Trial Comparing Electric and Harmonic Scalpel in Mastectomy
- Conditions
- Complication, Postoperative
- Interventions
- Procedure: Harmonic scalpelProcedure: Electric scalpel
- Registration Number
- NCT01391988
- Lead Sponsor
- Barretos Cancer Hospital
- Brief Summary
Prospective trial comparing post-operative complications and seroma formation after mastectomy in patients with breast cancer, using conventional electric scalpel and harmonic scalpel.
- Detailed Description
The population of this study was formed by women aged older than 18 years old, with breast carcinoma (ductal ou lobular) at any stage, form whom modified radical mastectomy is proposed. Patients were excluded if the present blood dyscrasia, collagen diseases, known uncontrolled chronic disease, infections (mammary or axillary, ulcerated tumors and pregnancy. The women were submitted to modified radical mastectomy consecutive allocated in electric scalpel group and the other group with harmonic scalpel.
Electric scalpels were calibrated at 40 watts of cutting and coagulation power and harmonic scalpel with a GEN04 generator calibrated at power levels 3 and 5, using the HP054 handpiece and HF105 curved blade.
Local postoperative complications analysed were seroma, hematoma, skin necrosis and infection.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 97
- Breast carcinoma (ductal or lobular)
- Modified radical mastectomy was the surgery to be realized
- Not inclusion criteria
- Blood dyscrasia, collagen diseases, known uncontrolled chronic diseases, infections (mammary or axillary), ulcerated tumors and pregnancy
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Harmonic scalpel mastectomy Harmonic scalpel Radical Mastectomy with harmonic scalpel Electric Scalpel Mastectomy Electric scalpel Radical mastectomy with electric scalpel
- Primary Outcome Measures
Name Time Method Differences in operative conditions and first week seroma drainage 1 week. Time of the surgery and blood loss volume during surgery. Drain volume postoperative in the first week
- Secondary Outcome Measures
Name Time Method Differences in local complication day 7 and day 14 Number of participants with adverse events as seroma, hematoma, skin necrosis and infection
Trial Locations
- Locations (1)
Hospital de Câncer de Barretos.
🇧🇷Barretos, São Paulo, Brazil