Assessment of Prophylactic Retention Suture in Preventing Dehiscence in Midline Laparotomy in High Risk Patient
Not Applicable
- Conditions
- Dehiscence.Disruption of operation wound, not elsewhere classified
- Registration Number
- IRCT201105082982N3
- Lead Sponsor
- Tehran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 300
Inclusion Criteria
undergoing midline laparotomy, being high risk for dehiscence or any other risk factors, informed consent for enrolling in the study, incision more than 10 cm
Exclusion criteria: age under 18, no informed consent, incision length for less than 10 cm
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Wound Dehiscence. Timepoint: Daily. Method of measurement: Clinical Examination.
- Secondary Outcome Measures
Name Time Method Wound Infection. Timepoint: Daily. Method of measurement: Clinical Examination.;Postoperative hospital stay. Timepoint: while discharge. Method of measurement: Based on hospital record.;Postoperative pain. Timepoint: Daily. Method of measurement: Visual analogue score.;Incisional Hernia. Timepoint: each 2 months till 6 month. Method of measurement: Clinical Examination.;Evisceration. Timepoint: Daily. Method of measurement: Clinical Examination.;Reoperation due to wound dehiscence. Timepoint: until 30 days postoperative. Method of measurement: Based on hospital record.;Mortality due to dehiscence. Timepoint: until 30 days postoperative. Method of measurement: Based on hospital record.