Open Versus Laparoscopic Repair of Perforated Peptic Ulcer
Not Applicable
Recruiting
- Conditions
- Perforated Peptic Ulcer
- Interventions
- Procedure: laparoscopic repair of perforated peptic ulcerProcedure: open repair of perforated peptic ulcer
- Registration Number
- NCT06484699
- Lead Sponsor
- Sohag University
- Brief Summary
The aim of this clinical trial is to compare the outcomes of open versus laparoscopic repair for perforated peptic ulcer and provide evidence-based guidance to the selection of the most appropriate operative technique at Sohag University Hospital. The study will include patients presented with perforated peptic ulcers as a complication of peptic ulcer disease during the period of study.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
- All patients with a clinical diagnosis of perforated peptic ulcer that are fit to undergo surgery either via laparotomy or laparoscopy, males or females, any age, with gastric or duodenal ulcer, with American Society of Anesthesiologists (ASA) grade I, II, III.
Exclusion Criteria
- Patients with associated bleeding ulcer (additional steps are needed to control bleeding).
- Patients with associated pathology other than perforated peptic ulcer.
- Patients with American Society of Anesthesiologists (ASA) grade IV, V, VI.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description laparoscopic repair of perforated peptic ulcer laparoscopic repair of perforated peptic ulcer group (B) includes patients with perforated peptic ulcer that will be operated by laparoscopic repair approach open repair of perforated peptic ulcer open repair of perforated peptic ulcer group (A) includes patients with perforated peptic ulcer that will be operated by open repair approach
- Primary Outcome Measures
Name Time Method Early postoperative follow up for repair of perforated peptic ulcer 3 days after the operation resumption of oral intake
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Sohag University Hospital
🇪🇬Sohag, Egypt