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出境医 / 临床实验 / Microbiologic Alterations of the Conjunctiva of Hot Tub-soaking Ophthalmologists (MACHO)

Microbiologic Alterations of the Conjunctiva of Hot Tub-soaking Ophthalmologists (MACHO)

Study Description
Brief Summary:
The purpose of this study is to determine if there are microbiologic alterations of the ocular surface after hot tub exposure. The study will evaluate the number of microbes before and after hot tub use in order to find out whether hot tub exposure has any change on the organisms present on the ocular surface. Participants will be randomized to dunk or not to dunk their head during their time in the hot tub.

Condition or disease Intervention/treatment Phase
Conjunctivitis, Bacterial Keratitis Bacterial Behavioral: Dunk Other: Exposure to Hot Tub Not Applicable

Detailed Description:

Keratitis is a rare destructive cause of blindness. It typically affects young and healthy individuals, is excruciatingly painful, and difficult to treat. With 60% of cases mis-diagnosed at presentation, acanthamoeba keratitis carries a far worse visual prognosis compared to other cornea infections. Exposure to hot tubs is a widely accepted risk factor. However, the mechanism of infection and prediction of who is at risk is unknown as the vast majority of hot tub users do not become infected.In vivo changes to ocular microbiology after hot tub exposure has never been described.

Changes to ocular microbiology after exposure to hot tubs have not been described. The purpose of this study is to investigate whether there are significant alterations in the microbiology of the conjunctiva after hot tub exposure that may contribute to these changes.

This study will recruit at least 34 subjects, who will be randomized to head submersion versus no head submersion, using at least three different hot tubs. A conjunctival swab, a minimal-risk test performed routinely in the eye clinic, will be performed before and after 15 minutes of hot tub exposure on one eye (randomized) per subject. The swabs will be plated on blood agar (bacterial cultures) and non-nutrient agar (acanthamoeba cultures).

In this prospective study, healthy subjects will be recruited. The study will be Health Insurance Portability and Accountability Act compliant and approved by the Institutional Review Board. All subjects will review and sign an informed consent form.

Each patient will have the conjunctiva of one eye (randomized) cultured. This practically no-risk technique entails touching a polyester-tip swab to the lining of the lower eyelid. Each subject will be randomized to head submersion or no head submersion; this exposure will be masked by the study coordinator. After 15 minutes of hot tub exposure, the subject will have the same eye swabbed for cultures.

Each sample (pre- and post-hot tub) will be randomly assigned a study number. One study coordinator will record and mask data. Water from each tub will be cultured.

The culture plates will be sent to our microbiology facility at UCSF and identification of organisms on the blood agar plates will be performed on our MALDI (mass spectrometry to identify bacteria and fungi). Non-nutrient agar plates will be plated with E. coli overlay and incubated for up to 7 days. The plates will be randomized and the microbiologists will be masked to exposures.

Study Design
Layout table for study information
Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 36 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Investigator, Outcomes Assessor)
Masking Description: A provider is assigned to perform conjunctival swabs; this person is completely masked to exposure. The culture plates, which are randomized, are sent to a microbiology lab and the technicians are completely masked to exposures when reading the plates.
Primary Purpose: Prevention
Official Title: Microbiologic Alterations of the Conjunctiva of Hot Tub-soaking Ophthalmologists
Actual Study Start Date : May 27, 2019
Actual Primary Completion Date : March 26, 2020
Actual Study Completion Date : March 26, 2020
Arms and Interventions
Arm Intervention/treatment
Experimental: Head Dunk
Subjects who are assigned to be in this arm are asked to sit in a hot tub for 15 minutes and instructed to submerge his or her head in the hot tub at least once and at least up to the eyebrows during his or her time in the hot tub.
Behavioral: Dunk
If randomized to "Dunk," the subject is asked to submerge his or her head in the hot tub at least up to brow level.

Other: Exposure to Hot Tub
Subjects will be asked to sit in a hot tub for 15 minutes (with an individual timer).

Placebo Comparator: No Head Dunk
Subjects assigned to this arm are asked to sit in a hot tub for 15 minutes but to keep his or her chin above water during the entire time.
Other: Exposure to Hot Tub
Subjects will be asked to sit in a hot tub for 15 minutes (with an individual timer).

Outcome Measures
Primary Outcome Measures :
  1. Quantity of organisms [ Time Frame: 1 year ]

    Genus-species will be identified for each sample, and quantified with an ordinal scale (0-4). The total of this score will be the quantity for that person-time. The primary analyses will be a Wilcoxon Rank Sum test (Mann-Whitney) between the two arms at the follow-up time point (randomized comparison of dunk vs no-dunk), and a Wilcoxon Signed Rank test between pre-hot-tub and post-hot-tub (longitudinal comparison of all cases).

    We estimate that a total of 20 subjects will provide 80% power to detect a 1.25 SD difference in the total quantity score between randomization arms at the post (f/u) time point. We estimate 80% power to detect a .9 SD difference between pre (baseline) and post (f/u) time points in a paired longitudinal analysis.



Secondary Outcome Measures :
  1. Richness (number of species per sample) of organisms found in the conjunctiva with hot tub use (post-test comparison) [ Time Frame: 1 year ]
    The investigators will assess whether organism diversity (richness) changes between arms (post-test comparison) using Simpson's Diversity, expressed in units of effective number (see Jost). We will also assess using Shannon's Diversity.

  2. Richness (number of species per sample) of organisms found in the conjunctiva with hot tub use (pre versus post) [ Time Frame: 1 year ]
    The investigators will assess whether organism diversity (richness) changes longitudinally (pre vs post-test comparison).

  3. Difference in organism profile with hot tub use (pre versus post) [ Time Frame: 1 year ]
    The investigators will determine whether the organism profile differs longitudinally (pre vs post-test comparison) using L-2 norm (Euclidean distance) and PERMANOVA. We will also assess using L-1 norm (Manhattan distance)

  4. Difference in organism profile with hot tub use (between arms) [ Time Frame: 1 year ]
    The investigators will determine whether the organism profile differs between arms (post-test comparison) using L-2 norm (Euclidean distance) and PERMANOVA. We will also assess using L-1 norm (Manhattan distance)

  5. Quantity comparing pre-hot tub and post-hot tub swabs [ Time Frame: 1 year ]
    We will compare quantity of organisms (amount and type) before and after hot tub use in both arms. We will used a paired t-test for analysis.

  6. Specific organisms found in the conjunctiva with hot tub use [ Time Frame: 1 year ]
    The investigators will compare specific organisms (Staphylococcus epidermidis, Corynebacterium species) between arms (post-test only) and longitudinally between time points (pre vs post-test) with Bonferroni correction


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:   Yes
Criteria

Inclusion criteria:

  • greater of 18 years of age
  • a willing participant
  • healthy

Exclusion criteria:

  • pregnancy
  • high or low blood pressure
  • active diarrhea
  • lymphedema
  • heart disease
  • seizure disorder.
Contacts and Locations

Locations
Layout table for location information
United States, California
UCSF
San Francisco, California, United States, 94122
Sponsors and Collaborators
University of California, San Francisco
Investigators
Layout table for investigator information
Principal Investigator: Gerami D Seitzman, MD UCSF/Proctor Foundation
Tracking Information
First Submitted Date  ICMJE June 5, 2019
First Posted Date  ICMJE June 14, 2019
Last Update Posted Date September 10, 2020
Actual Study Start Date  ICMJE May 27, 2019
Actual Primary Completion Date March 26, 2020   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures  ICMJE
 (submitted: June 13, 2019)
Quantity of organisms [ Time Frame: 1 year ]
Genus-species will be identified for each sample, and quantified with an ordinal scale (0-4). The total of this score will be the quantity for that person-time. The primary analyses will be a Wilcoxon Rank Sum test (Mann-Whitney) between the two arms at the follow-up time point (randomized comparison of dunk vs no-dunk), and a Wilcoxon Signed Rank test between pre-hot-tub and post-hot-tub (longitudinal comparison of all cases). We estimate that a total of 20 subjects will provide 80% power to detect a 1.25 SD difference in the total quantity score between randomization arms at the post (f/u) time point. We estimate 80% power to detect a .9 SD difference between pre (baseline) and post (f/u) time points in a paired longitudinal analysis.
Original Primary Outcome Measures  ICMJE Same as current
Change History
Current Secondary Outcome Measures  ICMJE
 (submitted: June 13, 2019)
  • Richness (number of species per sample) of organisms found in the conjunctiva with hot tub use (post-test comparison) [ Time Frame: 1 year ]
    The investigators will assess whether organism diversity (richness) changes between arms (post-test comparison) using Simpson's Diversity, expressed in units of effective number (see Jost). We will also assess using Shannon's Diversity.
  • Richness (number of species per sample) of organisms found in the conjunctiva with hot tub use (pre versus post) [ Time Frame: 1 year ]
    The investigators will assess whether organism diversity (richness) changes longitudinally (pre vs post-test comparison).
  • Difference in organism profile with hot tub use (pre versus post) [ Time Frame: 1 year ]
    The investigators will determine whether the organism profile differs longitudinally (pre vs post-test comparison) using L-2 norm (Euclidean distance) and PERMANOVA. We will also assess using L-1 norm (Manhattan distance)
  • Difference in organism profile with hot tub use (between arms) [ Time Frame: 1 year ]
    The investigators will determine whether the organism profile differs between arms (post-test comparison) using L-2 norm (Euclidean distance) and PERMANOVA. We will also assess using L-1 norm (Manhattan distance)
  • Quantity comparing pre-hot tub and post-hot tub swabs [ Time Frame: 1 year ]
    We will compare quantity of organisms (amount and type) before and after hot tub use in both arms. We will used a paired t-test for analysis.
  • Specific organisms found in the conjunctiva with hot tub use [ Time Frame: 1 year ]
    The investigators will compare specific organisms (Staphylococcus epidermidis, Corynebacterium species) between arms (post-test only) and longitudinally between time points (pre vs post-test) with Bonferroni correction
Original Secondary Outcome Measures  ICMJE Same as current
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title  ICMJE Microbiologic Alterations of the Conjunctiva of Hot Tub-soaking Ophthalmologists
Official Title  ICMJE Microbiologic Alterations of the Conjunctiva of Hot Tub-soaking Ophthalmologists
Brief Summary The purpose of this study is to determine if there are microbiologic alterations of the ocular surface after hot tub exposure. The study will evaluate the number of microbes before and after hot tub use in order to find out whether hot tub exposure has any change on the organisms present on the ocular surface. Participants will be randomized to dunk or not to dunk their head during their time in the hot tub.
Detailed Description

Keratitis is a rare destructive cause of blindness. It typically affects young and healthy individuals, is excruciatingly painful, and difficult to treat. With 60% of cases mis-diagnosed at presentation, acanthamoeba keratitis carries a far worse visual prognosis compared to other cornea infections. Exposure to hot tubs is a widely accepted risk factor. However, the mechanism of infection and prediction of who is at risk is unknown as the vast majority of hot tub users do not become infected.In vivo changes to ocular microbiology after hot tub exposure has never been described.

Changes to ocular microbiology after exposure to hot tubs have not been described. The purpose of this study is to investigate whether there are significant alterations in the microbiology of the conjunctiva after hot tub exposure that may contribute to these changes.

This study will recruit at least 34 subjects, who will be randomized to head submersion versus no head submersion, using at least three different hot tubs. A conjunctival swab, a minimal-risk test performed routinely in the eye clinic, will be performed before and after 15 minutes of hot tub exposure on one eye (randomized) per subject. The swabs will be plated on blood agar (bacterial cultures) and non-nutrient agar (acanthamoeba cultures).

In this prospective study, healthy subjects will be recruited. The study will be Health Insurance Portability and Accountability Act compliant and approved by the Institutional Review Board. All subjects will review and sign an informed consent form.

Each patient will have the conjunctiva of one eye (randomized) cultured. This practically no-risk technique entails touching a polyester-tip swab to the lining of the lower eyelid. Each subject will be randomized to head submersion or no head submersion; this exposure will be masked by the study coordinator. After 15 minutes of hot tub exposure, the subject will have the same eye swabbed for cultures.

Each sample (pre- and post-hot tub) will be randomly assigned a study number. One study coordinator will record and mask data. Water from each tub will be cultured.

The culture plates will be sent to our microbiology facility at UCSF and identification of organisms on the blood agar plates will be performed on our MALDI (mass spectrometry to identify bacteria and fungi). Non-nutrient agar plates will be plated with E. coli overlay and incubated for up to 7 days. The plates will be randomized and the microbiologists will be masked to exposures.

Study Type  ICMJE Interventional
Study Phase  ICMJE Not Applicable
Study Design  ICMJE Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Investigator, Outcomes Assessor)
Masking Description:
A provider is assigned to perform conjunctival swabs; this person is completely masked to exposure. The culture plates, which are randomized, are sent to a microbiology lab and the technicians are completely masked to exposures when reading the plates.
Primary Purpose: Prevention
Condition  ICMJE
  • Conjunctivitis, Bacterial
  • Keratitis Bacterial
Intervention  ICMJE
  • Behavioral: Dunk
    If randomized to "Dunk," the subject is asked to submerge his or her head in the hot tub at least up to brow level.
  • Other: Exposure to Hot Tub
    Subjects will be asked to sit in a hot tub for 15 minutes (with an individual timer).
Study Arms  ICMJE
  • Experimental: Head Dunk
    Subjects who are assigned to be in this arm are asked to sit in a hot tub for 15 minutes and instructed to submerge his or her head in the hot tub at least once and at least up to the eyebrows during his or her time in the hot tub.
    Interventions:
    • Behavioral: Dunk
    • Other: Exposure to Hot Tub
  • Placebo Comparator: No Head Dunk
    Subjects assigned to this arm are asked to sit in a hot tub for 15 minutes but to keep his or her chin above water during the entire time.
    Intervention: Other: Exposure to Hot Tub
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: September 2, 2020)
36
Original Estimated Enrollment  ICMJE
 (submitted: June 13, 2019)
34
Actual Study Completion Date  ICMJE March 26, 2020
Actual Primary Completion Date March 26, 2020   (Final data collection date for primary outcome measure)
Eligibility Criteria  ICMJE

Inclusion criteria:

  • greater of 18 years of age
  • a willing participant
  • healthy

Exclusion criteria:

  • pregnancy
  • high or low blood pressure
  • active diarrhea
  • lymphedema
  • heart disease
  • seizure disorder.
Sex/Gender  ICMJE
Sexes Eligible for Study: All
Ages  ICMJE 18 Years and older   (Adult, Older Adult)
Accepts Healthy Volunteers  ICMJE Yes
Contacts  ICMJE Contact information is only displayed when the study is recruiting subjects
Listed Location Countries  ICMJE United States
Removed Location Countries  
 
Administrative Information
NCT Number  ICMJE NCT03987178
Other Study ID Numbers  ICMJE 18-26141
Has Data Monitoring Committee No
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 University of California, San Francisco
Study Sponsor  ICMJE University of California, San Francisco
Collaborators  ICMJE Not Provided
Investigators  ICMJE
Principal Investigator: Gerami D Seitzman, MD UCSF/Proctor Foundation
PRS Account University of California, San Francisco
Verification Date September 2020

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