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Clinical Trials in Turkey / NCT06826209
Enrolling by invitation Observational

Comparison of Upper Extremity Functional Performance in Hemophilic and Healthy Children

NCT06826209 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2024-10-24
Last updated
2025-02-13

Condition(s) studied

HemophiliaUpper ExtremityStrengthPerformanceChildren

Study summary

The goal of this observational study is to evaluate the functional performance of the upper extremity joints (scapula, shoulder, elbow, and wrist) in haemophilic children and compare muscle strength and ADL limitations with healthy children.

Eligibility

Sex
MALE
Min age
7 Years
Max age
17 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Diagnosed with Hemophilia A or B * Receiving prophylaxis treatment (a routine treatment) * Negative for inhibitors at the time of enrollment Exclusion Criteria: * Positive for inhibitors at the time of enrollment * Acute elbow bleeding * History of acute muscle bleeding * History of surgery in any upper extremity joints * Having undergone radionuclide synovectomy

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Hacettepe Universit Ankara Ankara

More Hacettepe University trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06826209 on ClinicalTrials.gov ↗ ← All trials in Turkey