Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-26 @ 10:19 PM
Ignite Modification Date:
2025-12-26 @ 10:19 PM
NCT ID:
NCT06220812
Eligibility Criteria:
Inclusion Criteria:
1. Age ranges from 6 to 10 years of both genders.
2. All subjects have unilateral extension type II and III supracondylar humeral fracture requiring closed reduction and percutaneous pinning (CRPP).
3. The study will be start immediately after removal the splint.
4. Children clinically and medically stable.
5. Children able to follow verbal commands.
6. Children sample will represent those children who enrolled in schools and other not yet.
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Exclusion Criteria:
The patients will be excluded if they have one of the following criteria;
1. Previous soft tissue injury at the same affected side of fracture.
2. Presence of associated fractures on the ipsilateral or contralateral upper limb.
3. Active infection near the fracture site.
4. Children with congenital or acquired skeletal deformities in the upper limbs.
5. Children with neurological deficits such as convulsions, involuntary movements, receiving muscle relaxants.
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Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
6 Years
Maximum Age:
10 Years
Study:
NCT06220812
Study Brief:
Protocol Section:
NCT06220812