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Ocular Rosacea Biome Study (ORBS)

Primary Purpose

Ocular Rosacea, Antimicrobial Resistance

Status
Recruiting
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Doxycycline 40 MG ( 20mg twice daily)
Doxycycline 200 MG ( 100 mg twice daily)
Placebo
Sponsored by
University of California, San Francisco
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Ocular Rosacea

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Have symptomatic ocular disease attributed to ocular rosacea as the primary diagnosis
  • Ability to give informed consent
  • Be aged 18 years old or older

Exclusion Criteria:

  • Have an active ocular or systemic infection
  • Have a known allergy or intolerance to tetracycline antibiotics
  • Have had prior use of oral antibiotics within the last three months
  • Pregnancy or the possibility of becoming pregnant within the 8-week study medication timeline.

Sites / Locations

  • University of California, San FarnciscoRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Placebo Comparator

Arm Label

40mg of oral doxycycline

100mg of oral doxycycline

Placebo

Arm Description

Arm A will receive submicrobial dose doxycycline (40mg) administered as 20mg twice a day for 8 weeks

Arm B will receive 200mg of oral doxycycline administered as 100mg twice a day for 8 weeks

Arm C will receive a placebo twice a day for 8 weeks

Outcomes

Primary Outcome Measures

Frequency of Antimicrobial Resistance (AMR) genetic determinants
The frequency of AMR genetic determinants in rectal swab samples between arms will be compared, correcting for baseline

Secondary Outcome Measures

Differences in Simpson's diversity of the microbiome of the conjunctiva and gut
Simpson's diversity is the probability that any two randomly chosen reads will be for different organisms (at the genus level). This will be expressed in terms of effective number.
Ocular Surface Disease Index (OSDI) will be compared
Scores range from 0 to 100, with higher scores indicating greater symptom severity. Standard 12-question created by the Outcomes Research Group at Allergan Inc will be used.
Tear Breakup Time (TBUT) scores will be compared
Numbers representing how many seconds after a full blink a discontinuity in the tear film appears. Obtained with the Oculus keratography topographer This is a scale typically measured from 1-10, and the seconds correspond to the amount of time it takes for a tear film discontinuity to be observed. The lower the number the faster the tear break up and the worse the objective dry eye.

Full Information

First Posted
March 16, 2022
Last Updated
July 3, 2023
Sponsor
University of California, San Francisco
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1. Study Identification

Unique Protocol Identification Number
NCT05296837
Brief Title
Ocular Rosacea Biome Study
Acronym
ORBS
Official Title
ORBS: Ocular Rosacea Biome Study
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 22, 2023 (Actual)
Primary Completion Date
October 30, 2023 (Anticipated)
Study Completion Date
January 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of California, San Francisco

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Ocular rosacea is an inflammatory disease of the eyelids and ocular surface. Like the facial disease, the ocular condition is chronic and recurrent. Sequelae of ocular rosacea vary from mild to severe. Ocular rosacea may cause chronic eye redness, blepharitis, recurrent chalazia, dry eye, corneal erosion, corneal vascularization, and corneal ulceration. Rosacea affecting the cornea can result in vision loss. Prescription eye drops and ointments can be used topically to control mild ocular rosacea. However, severe disease, or rosacea that is not well controlled with local treatments is treated systemically. The most commonly used systemic treatment for rosacea is the bacteriostatic antibiotic doxycycline. Rosacea treatment doses of doxycycline vary widely. Treatment-dose doxycycline for systemic infections is 100mg twice a day. However, as rosacea is considered an inflammatory disease, doxycycline is often dosed at what is termed, sub-microbial dose doxycycline (SDD). Initially introduced in the oral medicine literature, SDD are doses 40mg and lower because systemic administration at this dose does not appear to alter the oral mucosa flora or increase resistance rates when given long-term for periodontal disease. Whereas 100mg doxycycline, even when given short term, may increase the percentage of culturable nasopharyngeal flora that is resistant to doxycycline. The FDA does not categorize SDD an antibiotic, stating this dosing is expected to exhibit only anti-inflammatory activity.
Detailed Description
Even though SDD is widely used for the treatment of rosacea, very little confirmatory data exists, to indicate if this dose alters any other systemic mucosa flora or increases antibiotic resistance rates. The classification of 40mg as "sub-microbial" has never been evaluated in patients diagnosed with ocular rosacea. Additionally, confirmation of a "sub-microbial" dose has not been investigated with more sophisticated genomics and resistance tools such as metagenomic deep sequencing (MDS). The goal of this proposal is to use MDS to determine whether SDD given to patients with ocular rosacea can be truly considered sub-microbial, or if a 40mg dose of doxycycline can in fact alter the microbiome of the conjunctiva and gut and increase resistance rates when prescribed for 8 weeks. The investigators plan to evaluate the effect of SDD on resistance and microbiome alteration through a randomized controlled masked trial. This is a randomized, controlled, masked trial comparing sub-microbial dose doxycycline, treatment dose Doxycycline, and placebo in the treatment of ocular rosacea. Participants will be recruited from the F.I. Proctor Foundation and the Ophthalmology clinics at the UCSF Wayne and Gladys Valley Center for Vision and consented for participation in an IRB-approved study protocol. Participants with a diagnosis of ocular rosacea (n=50) will be prospectively enrolled and randomized to one of three arms in a 2:2:1 fashion: Arm A will receive submicrobial dose doxycycline (40mg) administered as 20mg twice day for 8 weeks Arm B will receive 200mg of oral doxycycline administered as 100mg twice a day for 8 weeks Arm C will receive a placebo twice a day for 8 weeks

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ocular Rosacea, Antimicrobial Resistance

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Randomized controlled trial
Masking
ParticipantCare ProviderInvestigator
Masking Description
All patients will be masked to their SDD allocation and informed that they will be taking a pill by mouth twice a day. Participants taking 40mg doxycycline will be taking one 20mg doxycycline pill twice a day. Participants taking 200mg doxycycline will be taking 100mg twice a day. Participants allocated to placebo will be taking a placebo pill twice daily All examining physicians responsible for TBUT determination and ocular photography will be masked to patient allocation assignment. The study analyst only will have access to the randomization key.
Allocation
Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
40mg of oral doxycycline
Arm Type
Experimental
Arm Description
Arm A will receive submicrobial dose doxycycline (40mg) administered as 20mg twice a day for 8 weeks
Arm Title
100mg of oral doxycycline
Arm Type
Active Comparator
Arm Description
Arm B will receive 200mg of oral doxycycline administered as 100mg twice a day for 8 weeks
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Arm C will receive a placebo twice a day for 8 weeks
Intervention Type
Drug
Intervention Name(s)
Doxycycline 40 MG ( 20mg twice daily)
Intervention Description
Submicrobial dose doxycycline (40mg) to be administered as 20mg twice daily
Intervention Type
Drug
Intervention Name(s)
Doxycycline 200 MG ( 100 mg twice daily)
Intervention Description
200 mg dose doxycycline to be administered as 100mg twice daily
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo to be administered in tablet form twice daily
Primary Outcome Measure Information:
Title
Frequency of Antimicrobial Resistance (AMR) genetic determinants
Description
The frequency of AMR genetic determinants in rectal swab samples between arms will be compared, correcting for baseline
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Differences in Simpson's diversity of the microbiome of the conjunctiva and gut
Description
Simpson's diversity is the probability that any two randomly chosen reads will be for different organisms (at the genus level). This will be expressed in terms of effective number.
Time Frame
4 weeks , 8 weeks, 3 - 6 months
Title
Ocular Surface Disease Index (OSDI) will be compared
Description
Scores range from 0 to 100, with higher scores indicating greater symptom severity. Standard 12-question created by the Outcomes Research Group at Allergan Inc will be used.
Time Frame
4 weeks , 8 weeks, 3 - 6 months
Title
Tear Breakup Time (TBUT) scores will be compared
Description
Numbers representing how many seconds after a full blink a discontinuity in the tear film appears. Obtained with the Oculus keratography topographer This is a scale typically measured from 1-10, and the seconds correspond to the amount of time it takes for a tear film discontinuity to be observed. The lower the number the faster the tear break up and the worse the objective dry eye.
Time Frame
4 weeks , 8 weeks, 3 - 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Have symptomatic ocular disease attributed to ocular rosacea as the primary diagnosis Ability to give informed consent Be aged 18 years old or older Exclusion Criteria: Have an active ocular or systemic infection Have a known allergy or intolerance to tetracycline antibiotics Have had prior use of oral antibiotics within the last three months Pregnancy or the possibility of becoming pregnant within the 8-week study medication timeline.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Victoria Cavallino, MSPH
Phone
(415) 353-2800
Email
victoria.cavallino@ucsf.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gerami Seitzman, MD
Organizational Affiliation
University of California, San Francisco
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of California, San Farncisco
City
San Francisco
State/Province
California
ZIP/Postal Code
94143
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gerami Seitzman, MD
Phone
415-353-2800
Email
gerami.seitzman@ucsf.edu
First Name & Middle Initial & Last Name & Degree
Victoria Cavallino, MSPH
Email
victoria.cavallino@ucsf.edu

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
31150711
Citation
Schaller M, Kemeny L, Havlickova B, Jackson JM, Ambroziak M, Lynde C, Gooderham M, Remenyik E, Del Rosso J, Weglowska J, Chavda R, Kerrouche N, Dirschka T, Johnson S. A randomized phase 3b/4 study to evaluate concomitant use of topical ivermectin 1% cream and doxycycline 40-mg modified-release capsules, versus topical ivermectin 1% cream and placebo in the treatment of severe rosacea. J Am Acad Dermatol. 2020 Feb;82(2):336-343. doi: 10.1016/j.jaad.2019.05.063. Epub 2019 May 29. Erratum In: J Am Acad Dermatol. 2021 May;84(5):1506.
Results Reference
background
PubMed Identifier
28651825
Citation
Zhang M, Silverberg JI, Kaffenberger BH. Prescription patterns and costs of acne/rosacea medications in Medicare patients vary by prescriber specialty. J Am Acad Dermatol. 2017 Sep;77(3):448-455.e2. doi: 10.1016/j.jaad.2017.04.1127. Epub 2017 Jun 23.
Results Reference
background
PubMed Identifier
31251542
Citation
Nagler AR, Del Rosso J. The Use of Oral Antibiotics in the Management of Rosacea. J Drugs Dermatol. 2019 Jun 1;18(6):506.
Results Reference
background
PubMed Identifier
18561589
Citation
Del Rosso JQ, Schlessinger J, Werschler P. Comparison of anti-inflammatory dose doxycycline versus doxycycline 100 mg in the treatment of rosacea. J Drugs Dermatol. 2008 Jun;7(6):573-6. No abstract available.
Results Reference
background
PubMed Identifier
18315426
Citation
Preshaw PM, Novak MJ, Mellonig J, Magnusson I, Polson A, Giannobile WV, Rowland RW, Thomas J, Walker C, Dawson DR, Sharkey D, Bradshaw MH. Modified-release subantimicrobial dose doxycycline enhances scaling and root planing in subjects with periodontal disease. J Periodontol. 2008 Mar;79(3):440-52. doi: 10.1902/jop.2008.070375.
Results Reference
background
PubMed Identifier
12707093
Citation
Skidmore R, Kovach R, Walker C, Thomas J, Bradshaw M, Leyden J, Powala C, Ashley R. Effects of subantimicrobial-dose doxycycline in the treatment of moderate acne. Arch Dermatol. 2003 Apr;139(4):459-64. doi: 10.1001/archderm.139.4.459.
Results Reference
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Citation
Anon. Periostat [package insert]. Place of publication: Galderma; 2001
Results Reference
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PubMed Identifier
27861741
Citation
Schaller M, Almeida LM, Bewley A, Cribier B, Dlova NC, Kautz G, Mannis M, Oon HH, Rajagopalan M, Steinhoff M, Thiboutot D, Troielli P, Webster G, Wu Y, van Zuuren E, Tan J. Rosacea treatment update: recommendations from the global ROSacea COnsensus (ROSCO) panel. Br J Dermatol. 2017 Feb;176(2):465-471. doi: 10.1111/bjd.15173. Epub 2017 Feb 5.
Results Reference
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PubMed Identifier
34713539
Citation
Del Rosso JQ, Brantman S, Baldwin H. Long-term inflammatory rosacea management with subantibiotic dose oral doxycycline 40 mg modified-release capsules once daily. Dermatol Ther. 2022 Jan;35(1):e15180. doi: 10.1111/dth.15180. Epub 2021 Dec 2.
Results Reference
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PubMed Identifier
31936625
Citation
Woo YR, Lee SH, Cho SH, Lee JD, Kim HS. Characterization and Analysis of the Skin Microbiota in Rosacea: Impact of Systemic Antibiotics. J Clin Med. 2020 Jan 9;9(1):185. doi: 10.3390/jcm9010185.
Results Reference
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Ocular Rosacea Biome Study

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