Comparison of pain killer medicine with salt water injection when given after intestine surgery
Not Applicable
- Conditions
- Health Condition 1: null- Patients are the who have an ileostomy done previously and are now posted for ileostomy closure.
- Registration Number
- CTRI/2017/03/008192
- Lead Sponsor
- Basavatarakam IndoAmerican Cancer Hospital and Research Institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 70
Inclusion Criteria
All patients under American Society of Anaesthesiologists physical status I and II will be included in the trial and will undergo randomization.
Exclusion Criteria
Exclusion criteria will include patients unable or unwilling to give informed consent, those with a history of relevant drug allergy, those currently using analgesics or who have current acute or chronic pain or are receiving medical therapies considered to result in tolerance to opioids, and patients with coagulopathies.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare 24 hour morphine consumption in patients who undergo ileostomy closure with and without transversus abdominis plane block under ultrasound guidance.Timepoint: 24 hours
- Secondary Outcome Measures
Name Time Method TO compare visual analogue score at rest and movement, to compare nausea and vomiting postoperativelyTimepoint: 24 hours