Patient reported outcome following incisional hernia repair:A survey on 163 patients at two maximum care hospitals
- Conditions
- K43.0Incisional hernia with obstruction, without gangrene
- Registration Number
- DRKS00016634
- Lead Sponsor
- HELIOS Research Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 163
Inclusion Criteria
conducted incisional hernia repair
Exclusion Criteria
Wish of the patient to get excluded
Nonage (<16 years)
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Relapse of an incisional hernia one year after surgery <br>yes/no
- Secondary Outcome Measures
Name Time Method Induced immobility due to carrying an abdominal binder one year after surgery yes/no<br><br>Pain reducing effect of an abdominal binder one year after surgery yes/no
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 associated with incisional hernia recurrence in DRKS00016634 observational study?
How do patient-reported outcomes in DRKS00016634 compare to laparoscopic hernia repair in terms of quality of life and recurrence rates?
Are there biomarkers in DRKS00016634 that predict postoperative complications in K43.0 incisional hernia patients?
What adverse events are most frequently reported in DRKS00016634 following incisional hernia repair and their management strategies?
How does the use of synthetic mesh in incisional hernia repair correlate with long-term patient-reported outcomes in DRKS00016634?