Postoperative Care of Sutured Wounds
| Status: | Enrolling by invitation |
|---|---|
| Conditions: | Hospital |
| Therapuetic Areas: | Other |
| Healthy: | No |
| Age Range: | 18 - 65 |
| Updated: | 2/17/2019 |
| Start Date: | October 2015 |
| End Date: | October 1, 2019 |
Comparing the Efficacy of Hydrogen Peroxide Versus Normal Saline in Postoperative Care of Sutured Wounds
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.
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.
We found this trial at
1
site
Chicago, Illinois 60611
Click here to add this to my saved trials
