Comparing the pain relief effect of two types of pain killers in patients of hernia surgery
Not Applicable
Completed
- Conditions
- Health Condition 1: null- Male patients18 to 70 years Inguinal Hernia Surgery ASA 1 and 2 statusHealth Condition 2: O- Medical and Surgical
- Registration Number
- CTRI/2016/08/007217
- Lead Sponsor
- Government Medical College and Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Under going inguinal hernia surgery
ASA status I and II
Exclusion Criteria
1.ASA status > III
2.Major co-existing medical illness (especially severe asthma/COPD, epilepsy, uncontrolled hypertension or diabetes, liver or renal disease)
3.Patients with paralytic ileus
4.Patients on tricyclic antidepressants, anticonvulsants, Mono amino oxidase inhibitors, antipsychotics or serotonin-norepinephrine reuptake inhibitors (i.e. within 30 days)
5. Known hypersensitivity to any of the study medications.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain at rest and on movement measured by visual analog scale (VAS)Timepoint: During the postoperative period at intervals of 0 hour (when the first dose of the combination is administered, i.e., when the block level recedes to T10), 2, 4, 8, 12, and 24 h
- Secondary Outcome Measures
Name Time Method Haemodynamics,Patient Satisfaction Scale , rescue analgesics, adverse effectsTimepoint: During the postoperative period at intervals of 0 hour (when the first dose of the combination is administered, i.e., when the block level recedes to T10), 2, 4, 8, 12, and 24 h