Two drugs will be compared along with local anaesthetics in spinal anaesthesia.
Phase 3
- Conditions
- Health Condition 1: - Health Condition 2: M959- Acquired deformity of musculoskeletal system, unspecified
- Registration Number
- CTRI/2021/01/030252
- Lead Sponsor
- Subhaprada satapathy
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Adults in the age group of 18-65 years
2.ASA I or II
3.Elective lower limb surgeries
Exclusion Criteria
1.Body mass index >=30.
2.Height less than 155 cm.
3.Contraindications to spinal anaesthesia(patient refusal,coagulation disorder, infection at puncture site,increased intracranial tension, haemodynamic instability, spinal deformities,known history of allergy to the study drugs).
4.Patients on hypnotics,antipsychotics,tranquilizers or other CNS depressants.
5.Patients with history of adverse reaction to opioids.
6.Pregnancy.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the duration of effective analgesia between the two drugs(time from intrathecal injection till the requirement of first rescue analgesic)Timepoint: 1.5years
- Secondary Outcome Measures
Name Time Method 1.Intraoperative haemodynamic parameters. <br/ ><br>2.Post operative VAS <br/ ><br>3.Incidence of side effects like sedation, pruritus, nausea, vomiting. <br/ ><br>Timepoint: 1.5years