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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05286203
Other study ID # P0555674
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date June 6, 2022
Est. completion date December 2026

Study information

Verified date July 2022
Source University of California, San Francisco
Contact Jessica Shantha, MD
Phone (415) 476-1442
Email Jessica.shantha@ucsf.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a multi-center randomized controlled evaluator-masked trial designed to compare metagenomic deep sequencing (MDS) versus standard of care testing for improvement of outcomes for intraocular infections. Patients with presumed intraocular infections who meet the eligibility criteria will be randomized to receive MDS testing results or not to receive MDS testing results. All patients will receive standard-of-care testing to guide management. Enrolled patients will be followed at week 2, week 3-6 (randomization visit), and at 4 weeks after the randomization visit. The proportions of patients who received the appropriate therapy and the proportions of patients with improved outcome will be compared between arms. Patient quality of life, MDS performance, and the provider certainly of belief will be collected.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date December 2026
Est. primary completion date December 2026
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Presumed infectious anterior uveitis, or intermediate uveitis, or posterior uveitis, or panuveitis - Presumed post-operative endophthalmitis - Unilateral or bilateral - 18 years and older Exclusion Criteria: - Insufficient specimen for MDS - Age < 18 years of age - Pregnancy - Unable to consent

Study Design


Intervention

Device:
Metagenomic Deep Sequencing (MDS)
MDS is an RNA-seq based testing of ocular fluid or tissue to identify potential infectious pathogens including bacteria, fungi, parasites, and DNA and RNA viruses.
Diagnostic Test:
Standard of Care (SOC)
SOC includes any available diagnostic tests, such as Gram stain, cultures, PCRs, that are considered the appropriate testing based on the clinical findings.

Locations

Country Name City State
United States University of California San Francisco (UCSF) San Francisco California

Sponsors (5)

Lead Sponsor Collaborator
University of California, San Francisco University of California, Davis, University of California, Los Angeles, University of Nebraska, University of Utah

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Clinical improvement Dichotomous variable (Y/N) as assessed by a masked evaluator 4-week after randomization
Primary Appropriate therapy Dichotomous variable (Y/N) as determined by an independent expert panel 4-week after randomization
Secondary Provider certainty of belief Provider certainty of belief that the patient has an infection (continuous variable from 0 to 100%) 4-week after randomization
Secondary Patient quality of life As measured by National Eye Institute Vision Function Questionnaire (min = 0, max = 100; higher means better vision function) 4-week after randomization
Secondary Infection status Estimated through latent class analysis that compares MDS with traditional tests for presumed ocular infections. Sensitivity and specificity will be reported as percentage (%) 4-week after randomization
Secondary Provider quality of care As measured by the World Health Organization Quality of Life Abbreviated Questionnaire (min = 0, max = 100; higher means better quality of life). 4-week after randomization
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