ClinicalTrials.Veeva

Menu

Postoperative Care of Sutured Wounds

Northwestern University logo

Northwestern University

Status

Withdrawn

Conditions

Wound Healing

Treatments

Drug: 0.9% normal saline
Drug: 3% H2O2 solution

Study type

Interventional

Funder types

Other

Identifiers

NCT02383992
STU200234

Details and patient eligibility

About

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.

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

0 participants in 2 patient groups

Hydrogen Peroxide
Active Comparator group
Description:
Post-operative wound will be treated with 3% H2O2 solution, Subjects will also clean the sutured wounds with 3% H2O2 solution or twice daily then dress the wounds with petroleum jelly and a bandage.
Treatment:
Drug: 3% H2O2 solution
Saline
Active Comparator group
Description:
Post-operative wound will be treated with 0.9% normal saline. Subjects will also clean the sutured wounds with normal saline twice daily then dress the wounds with petroleum jelly and a bandage.
Treatment:
Drug: 0.9% normal saline

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems