Post operative pain relief in hernia surgery
Not Applicable
- Conditions
- Health Condition 1: null- ASA 1 and 2 patients undergoing hernioplasty surgeries
- Registration Number
- CTRI/2018/01/011544
- Lead Sponsor
- HEAD OF THE DEPARTMENT
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1 Patients aged 18-70 years undergoing unilateral hernioplasty surgery
2 ASA 1 and 2
3 Informed consent.
Exclusion Criteria
1 Patient refusal to block
2 bleeding disorders
3 local infection
4 ASA 3 and 4
5 patients allergic to local anaesthetic
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Duration of postoperative analgesia.Timepoint: Interval between the time of performance of block and the time of first analgesia.
- Secondary Outcome Measures
Name Time Method umber of supplemental analgesic requirementsTimepoint: 24 hour requirement of rescue analgesic - injection Tramadol.;Postoperative Numerical rating Pain scores(NRS) at 0,1,2,3,4,5,6,8,12,24 hours and the mean postoperative NRS score.Timepoint: Monitored for 24 hours after block performance