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 @ 4:16 AM
Ignite Modification Date:
2025-12-25 @ 4:16 AM
NCT ID:
NCT00641420
Eligibility Criteria:
Inclusion Criteria:
* Male or female voluntary patients between the ages of 18 and 59 with Fitzpatrick skin type IV-VI as verified by one of the investigators
* Patients with clinical diagnosis of ice pick, rolling, or boxcar type ane scarring
* Patients able to follow instructions
* If patient has a history of cold sores (herpes labialis) they must be willing to take prophylactic valtrex
* Written informed consent from the patients (Appendix II)
Exclusion Criteria:
* Children (less than 18 years old)
* Pregnant or lactating women
* Personal history of keloids or hypertrophic scarring
* Active acne requiring topical or oral therapy
* Accutane or other oral retinoid in past year
* Patients with a known allergy to lidocaine
* Allergy to valacyclovir in a patient that needs prophylaxis
* Patients with an unstable or non controlled underlying medical problem
* Patients who are not able to follow instructions
* Patients who have participated in a study within the 3 months prior to study entry
* Patients who refuse to give written informed consent
* Patients with a history of a pigmentary abnormality
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
59 Years
Study:
NCT00641420
Study Brief:
Protocol Section:
NCT00641420