sefulness of abdominal binders as postoperative treatment following incisional hernia repair in sublay technique
Not Applicable
Completed
- Conditions
- K43.2K43.99Incisional hernia without obstruction or gangrene
- Registration Number
- DRKS00017410
- Lead Sponsor
- Helios Klinikum Berlin-Buch
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Age > 18 years
Patients who underwent incisional hernia repair in sublay technique
Subscribed consent form
Exclusion Criteria
Pregnancy
No hernia gap closure intraoperative (as screening failure)
Physical and psychological condition which not allows to understand and/or subscribe consent form
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain on the 14. postoperative day using VAS-Score
- Secondary Outcome Measures
Name Time Method Quality of life one year after surgery<br>Relapse rate one year after surgery<br><br>Rate of seroma formation 2 weeks after surgery
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular pathways are affected by abdominal binders in postoperative incisional hernia recovery using sublay technique?
How effective are abdominal binders compared to standard postoperative care in sublay incisional hernia repair?
Which biomarkers predict hernia recurrence or improved outcomes with abdominal binder use after sublay repair?
What adverse events are associated with abdominal binders in sublay incisional hernia repair and how are they managed?
Are there combination therapies with abdominal binders that enhance recovery in K43.2/K43.99 incisional hernia patients post-sublay repair?