Cutaneous Scarring of Scalpel Versus Cautery
Recruitment status was Recruiting
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Purpose
Cutaneous scarring after elective surgery is a concern for surgeons of all types, perhaps even more so to plastic surgeons. Cautery is often used on the "cut" setting to make or extend incisions; however very few studies have looked at the results of these scars. The investigators' study aims are to compare standard scalpel incisions versus cautery incisions and to objectively compare the resultant scars in a prospective, randomized, controlled fashion.
| Condition | Intervention |
|---|---|
|
Scars |
Procedure: Cautery vs Active Control Arm (Scalpel) |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety Study Intervention Model: Parallel Assignment Masking: Single Blind (Subject) Primary Purpose: Treatment |
| Official Title: | A Pilot Study Comparing Cutaneous Scarring When Scalpel Versus Cautery is Used to Make Skin Incisions |
- The primary outcome measure is the Vancouver Scar Scale [ Time Frame: 12 months ] [ Designated as safety issue: No ]
- Visual scar scale done by both the subject and an independent observer [ Time Frame: 2 week ] [ Designated as safety issue: No ]
- Visual scar scale done by both the subject and an independent observer [ Time Frame: 3 months ] [ Designated as safety issue: No ]
- Visual scar scale done by both the subject and an independent observer [ Time Frame: 6 months ] [ Designated as safety issue: No ]
- Visual scar scale done by both the subject and an independent observer [ Time Frame: 12 months ] [ Designated as safety issue: No ]
| Estimated Enrollment: | 10 |
| Study Start Date: | November 2008 |
| Estimated Study Completion Date: | August 2011 |
| Estimated Primary Completion Date: | April 2011 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Active Comparator: Cautery Arm
Cautery to make skin incision
|
Procedure: Cautery vs Active Control Arm (Scalpel)
Interventions: The cautery used will be the standard operating room monopolar cautery used at our institution. The cautery will be used on a "cut" setting of 20 with a blend setting of zero (pure cut). A standard protected needle tip cautery will be used. A #15 blade carbon steel scalpel blade will be used on ½ of the incision; a cautery device with the above-mentioned settings will be used on the other ½ of the wound. The patient will be randomly assigned to receive the cautery incision on the left or right side. The same surgeon will make all of the skin incisions and perform the skin closures in order to provide as much standardization as possible. The closure will be standardized. Other Name: bovie
|
|
Active Comparator: Scalpel Incision
Scalpel to make skin incision
|
Procedure: Cautery vs Active Control Arm (Scalpel)
Interventions: The cautery used will be the standard operating room monopolar cautery used at our institution. The cautery will be used on a "cut" setting of 20 with a blend setting of zero (pure cut). A standard protected needle tip cautery will be used. A #15 blade carbon steel scalpel blade will be used on ½ of the incision; a cautery device with the above-mentioned settings will be used on the other ½ of the wound. The patient will be randomly assigned to receive the cautery incision on the left or right side. The same surgeon will make all of the skin incisions and perform the skin closures in order to provide as much standardization as possible. The closure will be standardized. Other Name: bovie
|
Show Detailed Description
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria: Inclusion Criteria:
- Patients undergoing primary, elective panniculectomy.
- Patients must voluntarily be enrolled in the study after informed consent.
- Patients must be in relative good health and have adequate nutrition.
- Patients of all races and genders will be included.
- Patients must agree to refrain from the use of topical scar products during the study period.
Exclusion Criteria:
- Under the age of 18 years old
- Patients with previous history of hypertrophic or keloid scarring
- Patients presenting for scar revision
- Patients presenting for a non-elective surgery
- Patients with chronic immunosuppression or wound healing problems
- Currently taking medications that interfere with wound healing such as corticosteroids, anti-coagulants (aspirin or NSAIDs), vasoconstricting agents (adrenaline or ergotrate), anti-cancer drugs, or colchicine for gout,
- Use of any tobacco products
Contacts and Locations| United States, Texas | |
| Scott and White Hospital and Clinic | Recruiting |
| Temple, Texas, United States, 76508 | |
| Contact: JoAnn Nichols 254-724-9187 jnichols@swmail.sw.org | |
| Principal Investigator: Raman C Mahabir, MD | |
| Principal Investigator: | Raman C Mahabir, MD | Scott and White Hospital & Clinic |
More Information
Publications:
| Responsible Party: | Raman Chaos Mahabir, MD, MSc, FRCSC, Scott and White Hospital |
| ClinicalTrials.gov Identifier: | NCT00803140 History of Changes |
| Other Study ID Numbers: | 81818CSSvC |
| Study First Received: | December 3, 2008 |
| Last Updated: | February 25, 2011 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by Scott and White Hospital & Clinic:
|
scarring |
Additional relevant MeSH terms:
|
Cicatrix Fibrosis Pathologic Processes |
ClinicalTrials.gov processed this record on May 23, 2013