Expired Study
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials.

Chicago, Illinois 60611


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.


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.



Primary Contact:

Principal Investigator
Murad Alam, MD
Northwestern University

Backup Contact:


Location Contact:

Chicago, Illinois 60611
United States

There is no listed contact information for this specific location.

Site Status: N/A

Data Source: ClinicalTrials.gov

Date Processed: January 21, 2020

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.

Click to view Full Listing

This study is not currently recruiting Study Participants on ClinicalConnection.com. The form below is not enabled.