Nailfold Capillaroscopic Assessment in Pediatric Uveitis Patients

February 1, 2024 updated by: Maha Sayed Ibrahim Abdelrahman, Assiut University
Pediatric uveitis accounts for 5-10% of uveitis cases. it may be infectious or noninfectious in etiology. The etiology of noninfectious uveitis may be autoimmune. The most common causes of pediatric uveitis are idiopathic and juvenile idiopathic arthritis-associated uveitis. Uveitis morbidities in pediatric patients include cataract, glaucoma, and amblyopia. Pediatric uveitis may be accopanied by involvement of the ocular vasculature, such as retinal vasculitis. We hypothesize that there are differences in systemic microcirculation between pediatric uveitis patients and healthy pediatric controls.

Study Overview

Status

Recruiting

Conditions

Detailed Description

The systemic microcirculation will be investigated through nailfold capillaroscopic (NFC) assessment with noninfectious uveitis and healthy pediatric controls.

The NFC parameters are:

capillary density (number of capillaries per mm), dilated capillaries (apex of >20µm), avascular areas, the presence of microhemorrhages, and capillary morphology (normal, multiple crossings, tortuous, bushy, ramified, non-convex, or bizarre capillaries).

Study Type

Observational

Enrollment (Estimated)

50

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

      • Assiut, Egypt, 71515
        • Recruiting
        • Maha Abdelrahman
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Probability Sample

Study Population

pediatric uveitis patients and healthy pediatric control

Description

Inclusion Criteria:

  • patients with uveitis < 18 years old

Exclusion Criteria:

  • infectious uveitis
  • age > 18 years old

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
pediatric uveitis
pediatric uveitis patients < 18 years old
healthy subjects
healthy subjects< 18 years old

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
capillary density by nailfold capillaroscopy
Time Frame: 6 months
(number of capillaries per mm)
6 months
detection of number of dilated capillaries by nailfold capillaroscopy
Time Frame: 6 months
number of dilated capillaries (apex of >20µm)
6 months
detection of other abnormalities as avascular areas, microhemorrhages, and abnormal capillary morphology
Time Frame: 6 months
detection of multiple crossings, tortuous, bushy, ramified, non-convex, or bizarre capillaries
6 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
correlation of nailfold findings with uveitis activity
Time Frame: 6 months
correlation of capillary abnormalities detected with active uveitis.
6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Maha Abdelrahman, MD, PHD, Assiut University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 15, 2024

Primary Completion (Estimated)

May 15, 2024

Study Completion (Estimated)

July 15, 2024

Study Registration Dates

First Submitted

October 1, 2023

First Submitted That Met QC Criteria

October 1, 2023

First Posted (Actual)

October 6, 2023

Study Record Updates

Last Update Posted (Estimated)

February 2, 2024

Last Update Submitted That Met QC Criteria

February 1, 2024

Last Verified

February 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • Nailfold capillaroscopy

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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