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出境医 / 临床实验 / Study Comparing Open Radical Cystectomy With Robot-assisted Cystectomy in Patients With Bladder Cancer

Study Comparing Open Radical Cystectomy With Robot-assisted Cystectomy in Patients With Bladder Cancer

Study Description
Brief Summary:
The purpose of the study to compare two established methods of radical cystectomy (RC) in patients with bladder cancer. The participants will be treated under conditions in alignment with up-to-date guidelines and care. We wish to investigate whether it is feasible to compare the two methods under conditions of the highest methodological quality.

Condition or disease Intervention/treatment Phase
Urinary Bladder Neoplasms Procedure: Radical Cystectomy Not Applicable

Detailed Description:

Radical cystectomy (RC) is a comprehensive surgery including pelvic lymph node dissection and urinary diversion. The surgery is originally performed as an open procedure (ORC) but with advances in technology the procedure is now also offered as a robot-assisted laparoscopic procedure (RARC). It remains questionable if RARC is superior to ORC in terms of surgical outcomes.

Several studies have described outcomes following RARC of which most are comparative studies with only five studies being randomized controlled trials (RCTs). Overall, significant differences in operating room time, estimated blood loss, time to flatus and bowel movement as well as use of morphine sulfate equivalents in favor of RARC has been demonstrated with the exception of operating room time. However, no studies have demonstrated a significant reduction in risk of 30- or 90-day complication rates between ORC and RARC. The RCTs have not been blinded, and therefore may be subject to bias in terms of expectations from patients and care providers. Also, in the already conducted RCTs of ORC versus RARC the urinary diversion has been done extracorporally. Today, it is possible to conduct the whole procedure of RARC intracorporally (iRARC), potentially reducing the surgical stress further. Lastly, the previously conducted RCTs have not consequently been managed under an Enhanced Recovery After Surgery (ERAS) setup. Currently, a multicenter study comparing ORC with RARC is recruiting in the United Kingdom in which the patients are treated with iRARC and under an ERAS setup. The present study will compare the two methods blinded for the participants and all health care providers involved in the postoperative care from the time the patient exits the operating room (OR). Blinded studies in surgery are rare but in gastrointestinal surgery, a blinded study of open versus laparoscopic colonic resection has demonstrated to be feasible and thus we believe that such study must be feasible in an RC setting.

Participants will be randomized 1:1 to either ORC or RARC. Blinding: The study is blinded for the patient and for the group of nurses and doctors that will be responsible for the postoperative care. The postoperative care will be managed by members of the bladder cancer team other than the operating surgeon, and OR staff will not be involved in the postoperative care. The abdominal wound will be bandaged to hide the wounds from both an open and laparoscopic procedure. The blinding will be maintained until discharge from hospital.

Study Design
Layout table for study information
Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 50 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Participant, Care Provider)
Primary Purpose: Treatment
Official Title: A Controlled Blinded Randomized Feasibility Study of Open Radical Cystectomy (ORC) Versus Robot-Assisted Radical Cystectomy With Intracorporal Urinary Diversion (iRARC) Under an Enhanced Recovery After Surgery (ERAS) Setup
Actual Study Start Date : June 6, 2019
Actual Primary Completion Date : November 1, 2020
Actual Study Completion Date : January 20, 2021
Arms and Interventions
Arm Intervention/treatment
Active Comparator: Open Radical Cystectomy (ORC)
Open radical cystectomy includes in both genders removal of the bladder and distal ureters as well as pelvic lymphadenectomy. In men the procedure includes removal of the prostate and seminal vesicles and in women removal of the uterus, ovaries, urethra and part of the vagina. Lastly, for both genders an iliac conduit urinary diversion is performed.
Procedure: Radical Cystectomy
Participants are randomly and blinded assigned

Active Comparator: Robot-assisted Radical Cystectomy (iRARC)
Robot-assisted radical cystectomy includes in both genders removal of the bladder and distal ureters as well as pelvic lymphadenectomy. In men the procedure includes removal of the prostate and seminal vesicles and in women removal of the uterus, ovaries, urethra and part of the vagina. Lastly, for both genders an intracorporeal iliac conduit urinary diversion is performed.
Procedure: Radical Cystectomy
Participants are randomly and blinded assigned

Outcome Measures
Primary Outcome Measures :
  1. Participants blinded at discharge [ Time Frame: 12 months ]
    Number of patients that was not unblinded at discharge


Secondary Outcome Measures :
  1. Length of Stay (LOS) [ Time Frame: 12 months ]
    Duration (days) of primary hospitalization. From the date of admission until the date of discharge from hospital.

  2. Days Alive and Out of Hospital (DAOH) [ Time Frame: 90 days from surgery ]
    Number of days alive and out of hospital within 90 days from surgery

  3. 30-day complication rate [ Time Frame: 30 days after surgery ]
    Complication rate (Clavien-Dindo)

  4. 90-day complication rate [ Time Frame: 90 days after surgery ]
    Complication rate (Clavien-Dindo)

  5. Readmission rate [ Time Frame: 90 days after surgery ]
    Number of readmissions

  6. Quality of Life (QoL): EORTC QLQ-C30 [ Time Frame: 90 days after surgery ]
    Registration of differences in QoL. European Organization for Research and Treatment of Cancer 30-item core quality of life questionnaire (EORTC QLQ-C30 (scale range 0-100, a higher score indicating better quality of life))

  7. Quality of Life (QoL): EORTC QLQ-BLM30 [ Time Frame: 90 days after surgery ]
    Registration of differences in QoL. European Organization for Research and Treatment of Cancer quality of life questionnaire for patients with muscle invasive bladder cancer (QLQ-BLM30 (scale range 0-100, a higher score indicating increase in symptom burden)) will be used.

  8. Blood loss [ Time Frame: 4 days after surgery ]
    Both estimated as well as calculated/hidden blood loss

  9. Use of opioids [ Time Frame: until diacharge or up to 90 days, whichever comes first ]
    Use of opioids, mg total postoperatively


Eligibility Criteria
Layout table for eligibility information
Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • age> 18
  • non-metastatic disease
  • fit for both ORC and RARC
  • Patient-selected urinary diversion: ileal conduit

Exclusion Criteria:

  • if not able to speak/understand Danish
  • not able to cooperate for fully informed consent
  • need for extensive concomitant surgery (i.e. nephroureterectomy)
  • prior down staging chemotherapy (prior neoadjuvant chemotherapy accepted)
  • prior radiation therapy
  • prior major extensive abdominal or pelvic surgery
  • prior peritonitis
  • conditions contraindicating extended Trendelenburg's position
Contacts and Locations

Locations
Layout table for location information
Denmark
Department of Urology, Rigshospitalet
Copenhagen, Denmark
Sponsors and Collaborators
Rigshospitalet, Denmark
Tracking Information
First Submitted Date  ICMJE May 29, 2019
First Posted Date  ICMJE June 6, 2019
Last Update Posted Date January 26, 2021
Actual Study Start Date  ICMJE June 6, 2019
Actual Primary Completion Date November 1, 2020   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures  ICMJE
 (submitted: June 5, 2019)
Participants blinded at discharge [ Time Frame: 12 months ]
Number of patients that was not unblinded at discharge
Original Primary Outcome Measures  ICMJE Same as current
Change History
Current Secondary Outcome Measures  ICMJE
 (submitted: January 22, 2021)
  • Length of Stay (LOS) [ Time Frame: 12 months ]
    Duration (days) of primary hospitalization. From the date of admission until the date of discharge from hospital.
  • Days Alive and Out of Hospital (DAOH) [ Time Frame: 90 days from surgery ]
    Number of days alive and out of hospital within 90 days from surgery
  • 30-day complication rate [ Time Frame: 30 days after surgery ]
    Complication rate (Clavien-Dindo)
  • 90-day complication rate [ Time Frame: 90 days after surgery ]
    Complication rate (Clavien-Dindo)
  • Readmission rate [ Time Frame: 90 days after surgery ]
    Number of readmissions
  • Quality of Life (QoL): EORTC QLQ-C30 [ Time Frame: 90 days after surgery ]
    Registration of differences in QoL. European Organization for Research and Treatment of Cancer 30-item core quality of life questionnaire (EORTC QLQ-C30 (scale range 0-100, a higher score indicating better quality of life))
  • Quality of Life (QoL): EORTC QLQ-BLM30 [ Time Frame: 90 days after surgery ]
    Registration of differences in QoL. European Organization for Research and Treatment of Cancer quality of life questionnaire for patients with muscle invasive bladder cancer (QLQ-BLM30 (scale range 0-100, a higher score indicating increase in symptom burden)) will be used.
  • Blood loss [ Time Frame: 4 days after surgery ]
    Both estimated as well as calculated/hidden blood loss
  • Use of opioids [ Time Frame: until diacharge or up to 90 days, whichever comes first ]
    Use of opioids, mg total postoperatively
Original Secondary Outcome Measures  ICMJE
 (submitted: June 5, 2019)
  • Length of Stay (LOS) [ Time Frame: 12 months ]
    Duration (days) of primary hospitalization. From the date of admission until the date of discharge from hospital.
  • Days Alive and Out of Hospital (DAOH) [ Time Frame: 90 days from surgery ]
    Number of days alive and out of hospital within 90 days from surgery
  • 30-day complication rate [ Time Frame: 30 days after surgery ]
    Complication rate (Clavien-Dindo)
  • 90-day complication rate [ Time Frame: 90 days after surgery ]
    Complication rate (Clavien-Dindo)
  • Readmission rate [ Time Frame: 90 days after surgery ]
    Number of readmissions
  • Quality of Life (QoL): EORTC QLQ-C30 [ Time Frame: 90 days after surgery ]
    Registration of differences in QoL. European Organization for Research and Treatment of Cancer 30-item core quality of life questionnaire (EORTC QLQ-C30 (scale range 0-100, a higher score indicating better quality of life))
  • Quality of Life (QoL): EORTC QLQ-BLM30 [ Time Frame: 90 days after surgery ]
    Registration of differences in QoL. European Organization for Research and Treatment of Cancer quality of life questionnaire for patients with muscle invasive bladder cancer (QLQ-BLM30 (scale range 0-100, a higher score indicating increase in symptom burden)) will be used.
  • Blood loss [ Time Frame: 4 days after surgery ]
    Both estimated as well as calculated/hidden blood loss
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title  ICMJE Study Comparing Open Radical Cystectomy With Robot-assisted Cystectomy in Patients With Bladder Cancer
Official Title  ICMJE A Controlled Blinded Randomized Feasibility Study of Open Radical Cystectomy (ORC) Versus Robot-Assisted Radical Cystectomy With Intracorporal Urinary Diversion (iRARC) Under an Enhanced Recovery After Surgery (ERAS) Setup
Brief Summary The purpose of the study to compare two established methods of radical cystectomy (RC) in patients with bladder cancer. The participants will be treated under conditions in alignment with up-to-date guidelines and care. We wish to investigate whether it is feasible to compare the two methods under conditions of the highest methodological quality.
Detailed Description

Radical cystectomy (RC) is a comprehensive surgery including pelvic lymph node dissection and urinary diversion. The surgery is originally performed as an open procedure (ORC) but with advances in technology the procedure is now also offered as a robot-assisted laparoscopic procedure (RARC). It remains questionable if RARC is superior to ORC in terms of surgical outcomes.

Several studies have described outcomes following RARC of which most are comparative studies with only five studies being randomized controlled trials (RCTs). Overall, significant differences in operating room time, estimated blood loss, time to flatus and bowel movement as well as use of morphine sulfate equivalents in favor of RARC has been demonstrated with the exception of operating room time. However, no studies have demonstrated a significant reduction in risk of 30- or 90-day complication rates between ORC and RARC. The RCTs have not been blinded, and therefore may be subject to bias in terms of expectations from patients and care providers. Also, in the already conducted RCTs of ORC versus RARC the urinary diversion has been done extracorporally. Today, it is possible to conduct the whole procedure of RARC intracorporally (iRARC), potentially reducing the surgical stress further. Lastly, the previously conducted RCTs have not consequently been managed under an Enhanced Recovery After Surgery (ERAS) setup. Currently, a multicenter study comparing ORC with RARC is recruiting in the United Kingdom in which the patients are treated with iRARC and under an ERAS setup. The present study will compare the two methods blinded for the participants and all health care providers involved in the postoperative care from the time the patient exits the operating room (OR). Blinded studies in surgery are rare but in gastrointestinal surgery, a blinded study of open versus laparoscopic colonic resection has demonstrated to be feasible and thus we believe that such study must be feasible in an RC setting.

Participants will be randomized 1:1 to either ORC or RARC. Blinding: The study is blinded for the patient and for the group of nurses and doctors that will be responsible for the postoperative care. The postoperative care will be managed by members of the bladder cancer team other than the operating surgeon, and OR staff will not be involved in the postoperative care. The abdominal wound will be bandaged to hide the wounds from both an open and laparoscopic procedure. The blinding will be maintained until discharge from hospital.

Study Type  ICMJE Interventional
Study Phase  ICMJE Not Applicable
Study Design  ICMJE Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Participant, Care Provider)
Primary Purpose: Treatment
Condition  ICMJE Urinary Bladder Neoplasms
Intervention  ICMJE Procedure: Radical Cystectomy
Participants are randomly and blinded assigned
Study Arms  ICMJE
  • Active Comparator: Open Radical Cystectomy (ORC)
    Open radical cystectomy includes in both genders removal of the bladder and distal ureters as well as pelvic lymphadenectomy. In men the procedure includes removal of the prostate and seminal vesicles and in women removal of the uterus, ovaries, urethra and part of the vagina. Lastly, for both genders an iliac conduit urinary diversion is performed.
    Intervention: Procedure: Radical Cystectomy
  • Active Comparator: Robot-assisted Radical Cystectomy (iRARC)
    Robot-assisted radical cystectomy includes in both genders removal of the bladder and distal ureters as well as pelvic lymphadenectomy. In men the procedure includes removal of the prostate and seminal vesicles and in women removal of the uterus, ovaries, urethra and part of the vagina. Lastly, for both genders an intracorporeal iliac conduit urinary diversion is performed.
    Intervention: Procedure: Radical Cystectomy
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status  ICMJE Completed
Actual Enrollment  ICMJE
 (submitted: June 5, 2019)
50
Original Estimated Enrollment  ICMJE Same as current
Actual Study Completion Date  ICMJE January 20, 2021
Actual Primary Completion Date November 1, 2020   (Final data collection date for primary outcome measure)
Eligibility Criteria  ICMJE

Inclusion Criteria:

  • age> 18
  • non-metastatic disease
  • fit for both ORC and RARC
  • Patient-selected urinary diversion: ileal conduit

Exclusion Criteria:

  • if not able to speak/understand Danish
  • not able to cooperate for fully informed consent
  • need for extensive concomitant surgery (i.e. nephroureterectomy)
  • prior down staging chemotherapy (prior neoadjuvant chemotherapy accepted)
  • prior radiation therapy
  • prior major extensive abdominal or pelvic surgery
  • prior peritonitis
  • conditions contraindicating extended Trendelenburg's position
Sex/Gender  ICMJE
Sexes Eligible for Study: All
Ages  ICMJE 18 Years and older   (Adult, Older Adult)
Accepts Healthy Volunteers  ICMJE No
Contacts  ICMJE Contact information is only displayed when the study is recruiting subjects
Listed Location Countries  ICMJE Denmark
Removed Location Countries  
 
Administrative Information
NCT Number  ICMJE NCT03977831
Other Study ID Numbers  ICMJE H-18056682-D
Has Data Monitoring Committee Not Provided
U.S. FDA-regulated Product
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
IPD Sharing Statement  ICMJE
Plan to Share IPD: No
Responsible Party Ulla Nordström Joensen, Rigshospitalet, Denmark
Study Sponsor  ICMJE Rigshospitalet, Denmark
Collaborators  ICMJE Not Provided
Investigators  ICMJE Not Provided
PRS Account Rigshospitalet, Denmark
Verification Date January 2021

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP

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