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Clinical Trials/DRKS00011733
DRKS00011733
Recruiting
Phase 4

Postoperative intra-abdominal adhesion prophylaxis with 4DryField® PH – a randomised, controlled, prospective, monocentric observational study with 4DryField® PH only including patients with open abdominal surgeries

PlantTec Medical GmbH0 sites40 target enrollmentMarch 14, 2017

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Adhesion prevention after abdominal surgery
Sponsor
PlantTec Medical GmbH
Enrollment
40
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 14, 2017
End Date
TBD
Last Updated
last year
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Open surgery, because of one of the following reasons: Intra\-abdominal perforation in general, perforation of hollow organs (gall, stomach, intestine), complicated diverticulitis, intra\-abdominal adhesions, intestinal fistulas, anastomotic insufficiency; additionally: compliance of the patient, written consent of the patient

Exclusion Criteria

  • Intolerance of substances containing starch, pregnancy, missing compliance, missing written consent of the patient, missing legal capacity, participation in different studies that could interfere with the results of this study

Outcomes

Primary Outcomes

Not specified

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