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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT02383992
Other study ID # STU200234
Secondary ID
Status Withdrawn
Phase N/A
First received
Last updated
Start date October 2015
Est. completion date October 1, 2019

Study information

Verified date December 2021
Source Northwestern University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The primary objective of this study is to compare the efficacy of hydrogen peroxide versus normal saline in postoperative care of sutured wounds. Subjects will be randomly assigned to standard of care hydrogen peroxide or standard of care normal saline in postoperative care of sutured wounds followed by applying petroleum jelly and sterile gauze bandage. Data will be collected at day 0 and between days 7 to14. Subjects will provide irritation scale rating (0-4) with 0 being none/absent and 4 being severe/extreme.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date October 1, 2019
Est. primary completion date October 1, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: 1. Patients who are undergoing sutured wound after dermatologic procedure. 2. Males and females ages 18-65 years old. 3. Patients who are in good health. 4. Willingness and the ability to understand and provide informed consent and communicate with the investigator/study staff. Exclusion Criteria: 1. History of keloids or hypertrophic scars. 2. History of bleeding tendency or coagulopathy. 3. Pregnant or lactating or intends to become pregnant in the next 3 months. 4. Active skin disease or skin infection in the treatment area. 5. Unable to understand the protocol or to give informed consent. 6. Any other condition that would, in the professional opinion of the investigator, potentially affect response or participation in the clinical clinical study, or would pose as an unacceptable risk to the subject.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
3% H2O2 solution

0.9% normal saline


Locations

Country Name City State
United States Northwestern University Feinberg School of Medicine, Department of Dermatology Chicago Illinois

Sponsors (1)

Lead Sponsor Collaborator
Northwestern University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Irritation scale rating from 1-2 weeks compared to baseline Subjects will provide irritation scale rating (0-4) with 0 being none/absent and 4 being severe/extreme. Baseline and 1-2 weeks
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