A CLINICAL TRIAL TO STUDY THE EFFICACY OF TWO BLOCKS FOR LUMBAR DISECTOMY SURGERIES
Not Applicable
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/01/039249
- Lead Sponsor
- IMS BH
- 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
Cases of prolapsed intervertebral disc(PIVD) undergoing disectomy
Exclusion Criteria
Patientâ??s age <25 years and >50 years.
Patients with Bleeding diasthesis.
Patient allergic to LA agents.
Patients with Psychiatric disorders.
Presence of infection at the injection area.
Patients with H/O previous spine surgeries.
Refusal of consent
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Visual analogue scaleTimepoint: 30 minutes,hours 1,6,12,24
- Secondary Outcome Measures
Name Time Method Total rescue analgesia requirement in 24 hoursTimepoint: 24 hours