A clinical trial to study the feasibility and safety of Adapted Enhanced Recovery After Surgery Pathway as compared to standard care in patients undergoing simple closure of perforated duodenal ulcer
Not Applicable
- Conditions
- Health Condition 1: null- patients of perforated duodenal ulcer undergoing primary closure
- Registration Number
- CTRI/2015/02/005548
- Lead Sponsor
- JIPMER
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 70
Inclusion Criteria
all consecutive patients more than 18 years undergoing simple closure of perforated peptic ulcer less than 10mm in size
Exclusion Criteria
Age less than 18 years
presence of any psychiatric or neurological illness
ASA class 3 or 4
irreversible septic shock
pregnancy
Spontaneously sealed off perforations that did not require surgical repair
multiple perforated peptic ulcers
Patients having concomitant definitive surgery or additional procedures done eg TV with GJ
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the length of hospitalisation (LOH) in patients managed with ERAS protocol vs standard practiceTimepoint: To compare the length of hospitalisation (LOH) in patients managed with ERAS protocol vs standard practice
- Secondary Outcome Measures
Name Time Method the time elapsed until resumption of oral feeding, the need for nasogastric tube reinsertion , the need for extra analgesics , the readmission and reoperation rates <br/ ><br>mortality and morbidity during the first 30 days after surgery.Timepoint: DURING HOSPITAL STAY