Status:
TERMINATED
Impact of Marking Surgical Incision on Patient's Abdomen
Lead Sponsor:
AdventHealth
Conditions:
Surgical Procedure
Eligibility:
FEMALE
18-89 years
Phase:
NA
Brief Summary
This is a study looking at patient's satisfaction with incision site and location after undergoing minimally invasive gynecologic surgery. (Laparoscopy) The study group will have the anticipated incis...
Detailed Description
This study is a prospective, randomized controlled trial examining the impact of marking the patient abdomen at the time of the preoperative visit on patient's satisfaction with scar appearance and sy...
Eligibility Criteria
Inclusion
- Age 18 - 89
- Diagnosed with a benign surgical pathology
- Patient scheduled for elective minimally invasive gynecologic surgery
Exclusion
- Have a diagnosis of gynecologic cancer
- History of prior laparoscopic surgery
- Emergency surgery
- Inability to provide informed consent
- Unable to follow up in the office for post operative visits
- Skin hypersensitivity or allergy to marker dye
- Positive pregnancy test
Key Trial Info
Start Date :
June 1 2012
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 8 2013
Estimated Enrollment :
4 Patients enrolled
Trial Details
Trial ID
NCT01803334
Start Date
June 1 2012
End Date
July 8 2013
Last Update
September 30 2020
Active Locations (1)
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1
Florida Hospital
Orlando, Florida, United States, 32804