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:
2025-12-25 @ 1:45 AM
Ignite Modification Date:
2025-12-25 @ 1:45 AM
NCT ID:
NCT06681194
Eligibility Criteria:
Inclusion Criteria:
* Patients must be 18 years or older.
* Patients must be admitted to the institution with non-infected, traumatic wounds exhibiting hypergranulation tissue.
* Patients must provide consent to participate in the study.
* Eligible wounds include superficial or partial-thickness wounds.
* Wounds will be categorized based on size and depth, with variations controlled for in the statistical analysis.
Exclusion Criteria:
* Patients with known allergies or contraindications to silver nitrate or triamcinolone.
* Patients with wounds that do not exhibit hypergranulation tissue.
* Patients with wounds not primarily due to traumatic injury (e.g., surgical wounds, pressure ulcers).
* Full-thickness, infected, or complex wounds will be excluded, as these may require different management strategies.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT06681194
Study Brief:
Protocol Section:
NCT06681194