Comparison between two techniques for post-operative pain relief after laparoscopic hernia surgery.
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/04/065381
- Lead Sponsor
- Department of Anaesthesiology IPGMER and SSKM Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Patients that have given written, informed consent to participate in the study.
2. American society of anaesthesiologist (ASA) physical status I-II.
3. Age 18-65 years old.
4. Body mass index below 30 kg/m2
5. Patients undergoing elective laparoscopic hernia surgery
Exclusion Criteria
1. The chronic use of analgesics or anti inflammatory drugs
2. Allergy to local anesthetics or any of the study drugs.
3. History of co-morbidities ( MI, asthma, COPD etc)
4. Pregnancy or lactation.
5. Patients with thrombocytopenia, coagulopathies, infection at site of block.
6. Inability to communicate due to dementia, language barrier or end stage disease.
7. Refusal to participate in study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Compare postoperative hospital stay between groups received ultrasound guided rectus sheath block and transversus abdominis plane block.Timepoint: Post-operatively at 1,4,8,12,24 hours respectively.
- Secondary Outcome Measures
Name Time Method 1.To determine post-operative analgesia use. <br/ ><br>2.To determine post-operative hemodynamics. <br/ ><br>3.To determine the incidence of adverse events.Timepoint: Post-operatively at 1,4,8,12,24 hours respectively.