Evaluation of Cohera TissuGlu in the Management of Wound Drainage Following Abdominoplasty

NCT ID: NCT01331798

Last Updated: 2011-04-08

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 40 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2009-12-31
• Study Completion Date: 2010-05-31

Brief Summary

A blinded, prospective, randomized trial in 40 abdominoplasty cases at three sites to study the safety and the preliminary efficacy of TissuGlu®, a novel surgical adhesive, in the management of wound drainage during abdominoplasty procedures.

Detailed Description

Background: Fluid accumulation in dissected tissue planes has been a longstanding problem following surgical procedures. The common use of closed suction drains has been associated with infection risk, wound healing complications, additional scarring, and patient discomfort. Additionally, seroma formation after drain removal often requires invasive treatment. Therapies that can reduce fluid accumulation and decrease the need for drains will have a positive impact on surgical practice.

Objective: To study the safety and the preliminary efficacy of a TissuGlu®, a novel surgical adhesive, in the management of wound drainage during abdominoplasty procedures.

Material & Methods: A blinded prospective randomized trial compared drain fluid output (volume) and complication profile in 40 subjects undergoing abdominoplasty with (n=20) or without (n=20) the use of a urethane based adhesive. The TissuGlu® adhesive, which required no mixing or preparation, was administered to the abdominal wall using a custom drop tip applicator prior to closure of the abdominoplasty flap. Two Blake® drains connected to J-VAC suction reservoirs were placed in the wound.

Conditions

Abdominoplasty

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

Test: TissuGlu Adhesive

Patients received the TissuGlu Adhesive Treatment

Group Type: EXPERIMENTAL

Cohera TissuGlu Surgical Adhesive

Intervention Type: DEVICE

TissuGlu device used prior to closing of the flap in the abdominoplasty procedure.

Control

Control Arm received no TissuGlu- Standard of Care received.

Group Type: ACTIVE_COMPARATOR

Control- Standard of care

Intervention Type: PROCEDURE

Control Arm- no TissuGlu device used. Standard abdominoplasty procedure followed.

Interventions

Cohera TissuGlu Surgical Adhesive

TissuGlu device used prior to closing of the flap in the abdominoplasty procedure.

Intervention Type: DEVICE

Control- Standard of care

Control Arm- no TissuGlu device used. Standard abdominoplasty procedure followed.

Intervention Type: PROCEDURE

Eligibility Criteria

Inclusion Criteria

• Be at least 20 years of age;
• Be in good general health in the opinion of the Investigator with no conditions that would significantly impact wound healing as determined by medical history and review of recent concomitant medications;
• Be scheduled for at least one full thickness surgical incision of at least 20cm in length as part of elective abdominoplasty requiring the placement of sutures in the superficial fascia and subcutaneous tissue to relieve skin tension prior to final skin closure, Surgeon must use electrocautery in the procedure;
• Be willing to follow instructions for incision care, comply with schedule for wound drainage volume measurements, and follow guidelines related to resumption of daily activities;
• Agree to return for all follow-up evaluations specified in this protocol;
• Agree not to schedule any additional elective surgical procedures that involve an incision until their participation in this study is complete; and
• Sign the informed consent.

Exclusion Criteria

• Anesthesia Risk judged to be higher than ASA2
• Previous Abdominoplasty
• Have severe co-morbid conditions that pose a high risk for surgery and adequate recovery (e.g., heart disease)
• Any condition involving compromised vascular flow to the abdominal wall tissue. Prior abdominal scars, especially subcostal scars, will be a relative contraindication and judged on a case by case basis by the surgeon investigator.
• Any condition known to effect wound healing, such as collagen vascular disease
• Current active tobacco use, including smokeless (chewing) tobacco
• Obesity, as defined by BMI >30
• Known blood clotting disorder
• Current diagnosis of diabetes
• Be receiving antibiotic therapy for pre-existing condition or infection
• Have known personal or family history of keloid formation or hypertrophy
• Undergoing concurrent adjacent or congruent Liposuction procedures
• Concurrent use of fibrin sealants or other internal wound care devices
• Be currently taking systemic steroids or immunosuppressive agents
• Concurrent hernia repair greater than 6 cm and/or requiring the use of mesh
• Mini abdominoplasty (Abdominoplasty without umbilical transposition)
• Have known or suspected allergy or sensitivity to any test materials or reagents
• Be participating in any current clinical trial or have participated in any clinical trial within 30 days of enrollment in this study
• Pregnancy (30 days post-op)

• Minimum Eligible Age: 20 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Cohera Medical, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Cohera Medical Inc.

Locations

University of Bonn

Bonn, , Germany

Rosenpark Klinik

Darmstadt, , Germany

Erich-Lexer-Klinik

Freiburg im Breisgau, , Germany

Countries

Germany

Other Identifiers

PRO-100-0002

Identifier Type: -

Identifier Source: org_study_id