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Clinical Trials/NCT02010996
NCT02010996
Completed
Not Applicable

Preventing Seroma Formation After Stripping Saphenous Vein in Coronary Bypass - a Randomized Control Clinical Trial

Changhai Hospital1 site in 1 country72 target enrollmentDecember 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Coronary Bypass Graft Stenosis of Autologous Vein
Sponsor
Changhai Hospital
Enrollment
72
Locations
1
Primary Endpoint
Early Complications of Vascular Zone
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

The great saphenous vein is the most commonly used material in coronary vascular bridging operation. Coronary bypass operation to obtain the great saphenous vein is mainly through the incision open groin to ankle. This operation may damage the lymphatic, cause lymph circumfluence obstacle, cause fat liquefaction, scar formation, wound dehiscence, around hematoma and other a series of symptoms.Based on some studies and our experience that vacuum assisted closure (VAC)is effective in complex wound failures following Stripping saphenous vein, we use VAC to prevent seroma formation after Stripping saphenous vein in Coronary bypass. This study is aimed to evaluate the efficacy and economics benefits of early VAC application on postoperative complications and wound healing after Stripping saphenous vein in Coronary bypass in comparison to conventional suction drain.

Registry
clinicaltrials.gov
Start Date
December 2013
End Date
April 2014
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Bi-Hongda

physician

Changhai Hospital

Eligibility Criteria

Inclusion Criteria

  • Written informed consent
  • Coronary heart disease patients to transplant more than 2 vascular bridge
  • The thigh groin following from the saphenous vein

Exclusion Criteria

  • Subjects does not agree to participate in clinical trials
  • Subjects had a injury, operation history of Thigh
  • Subjects having ever received chemotherapy before the surgery
  • Subjects with known hypersensitivity to components of the surgical sticky membrane

Outcomes

Primary Outcomes

Early Complications of Vascular Zone

Time Frame: 2 weeks

Study Sites (1)

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