Comparison between two anesthetic blocks for postoperative pain relief in hernia patients.
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/01/061690
- Lead Sponsor
- Chettinad Hospital and Research Institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patient coming for Inguinal hernia repair under spinal anesthesia under American society of Anesthesiologists(ASA) grade I,II,III .
2.Patient scheduled for both elective and emergency studies
Exclusion Criteria
1. Patient refusal
2. If the duration of surgery is more than 3 hours
3. Contraindications to regional anesthesia
4. Known allergy to local anesthetics
5. Bleeding diathesis
6. Use of any anti-coagulants
7. Inability to provide informed consent
8. Severe kidney or liver disease
9. Patient with psychiatric disorders
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the duration of analgesic effect of transverse abdominus plane block and erector spinae block as post operative analgesia in patients undergoing inguinal hernia repair under spinal anesthesia. <br/ ><br>Timepoint: First 24 hours
- Secondary Outcome Measures
Name Time Method 1. To determine the total requirement of opioids as rescue analgesia in the first 24 hours <br/ ><br>2. To compare the hemodynamic stability of transverse abdominus block and erector spinae block <br/ ><br>3. To assess the post operative pain severity using visual analog score at rest and after coughTimepoint: First 24 hours