Hemostasis after abdominal wall surgery with 4DryField® PH

Phase 4

• Conditions: Wound healing disorderSermon; T81.0; T81.4; Haemorrhage and haematoma complicating a procedure, not elsewhere classified; Infection following a procedure, not elsewhere classified

• Registration Number: DRKS00012547
• Lead Sponsor: PlantTec Medical GmbH

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2017-04-01
• Study Start: 2018-01-05
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

1. Written consent to participate in the study,
2. Anterior abdominoplasty or lower Bodylift after Lockwood

Exclusion Criteria

1. Less extensive surgical procedure, 2. Intolerance to starch

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Postoperative blood loss, measured as total volume of the drainages until the drainage is removed

Secondary Outcome Measures

Name	Time	Method
1. Fraction of patients with wound infections, 2. Fraction of patients with seromas, 3. Fraction of patients with wound healing disturbances<br>(Appearances are recorded up to the end of the studies)<br>