To assess efficacy of steroid as adjuvant added to local anaesthetic in regional technique for pain management in laproscopic inguinal hernia repair- a randomized controlled prospective study
Phase 2
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/03/063593
- Lead Sponsor
- Fortis Hospital, Mohali
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA Grade 1 & 2
Patients in age group of 18-65 years posted for laproscopic inguinal hernia surgery
Willing to participate
Exclusion Criteria
Patient refusal
History of allergy or contraindication to study medicine
ASA Grade 3 & 4
Drug or Alcohol abuse
Surgery converted to open procedure
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the time of First rescue analgesia post-operatively <br/ ><br>Evaluate total doses of rescue analgesia in 24 hrsTimepoint: VAS scores will be assessed at 0hr,2hr,4hr,8hr,12hr,16hr,24hr <br/ ><br>Total dose of rescue analgesia will be assessed in 24 hrs
- Secondary Outcome Measures
Name Time Method Evaluate efficacy of TAP block in providing post-operative analgesia in laproscopic inguinal hernia surgeries <br/ ><br>Evaluate safety and adverse effects of TAP block <br/ ><br>Assess pain severity using Visual Analogue score(VAS score) <br/ ><br>Post-operative opioid consumptionTimepoint: 0hr,2hr,4hr,8hr,16hr,24hr