- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06070935
Nailfold Capillaroscopic Assessment in Pediatric Uveitis Patients
Study Overview
Status
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
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Maha Abdelrahman, PHD
- Phone Number: 01011212050
- Email: mahasayed@aun.edu.eg
Study Contact Backup
- Name: Maha Abdelrahman, MD, PHD
- Phone Number: 01011212050
- Email: mahasayed@aun.edu.eg
Study Locations
-
-
-
Assiut, Egypt, 71515
- Recruiting
- Maha Abdelrahman
-
Contact:
- Maha Abdelrahman, MD, PHD
- Phone Number: 01011212050
- Email: mahasayed@aun.edu.eg
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- patients with uveitis < 18 years old
Exclusion Criteria:
- infectious uveitis
- age > 18 years old
Study Plan
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
Sponsor
Investigators
- Principal Investigator: Maha Abdelrahman, MD, PHD, Assiut University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
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
Studies a U.S. FDA-regulated device product
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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