A study to compare the effect of two drugs used for giving spinal anaesthesia to perform surgeries below the level of umbilicus.
Phase 3
- Conditions
- Health Condition 1: V039- Pedestrian injured in collision with car, pick-up truck or van, unspecified whether traffic or nontraffic accident
- Registration Number
- CTRI/2024/03/064520
- Lead Sponsor
- Pandit BD Sharma PGIMS Rohtak
- 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 and Grade 2 patients posted for infraumbilical surgeries.
Exclusion Criteria
Age less than 18 years and more than 60 years.
ASA Grade 3 and above patients.
Patient allergic to the interventional drugs.
Patient not willing to participate in the research.
Patient having any neurological disease linked with brain and spinal cord.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Assessing the time of onset of sensory blockade and time of onset of motor blockade after subarachnoid injection of the study drugs (hyperbaric levo-bupivacaine and hyperbaric ropivacaine) and comparing the data.Timepoint: At one minute interval after administation of study drugs till 20 minutes.
- Secondary Outcome Measures
Name Time Method Assessment of the time required for two segments regression & complete regression of sensory blockade & complete regression of motor blockade in the two groups receiving the study drugs & time of first rescue analgesia requirement in the two groups will be done. Haemodynamic variations caused by the study drugs in the two groups will be noted. The quality of post operative analgesia in the two groups will be assessed & any adverse effects caused by the study drugs in the two groups will be noted. Data will be collected & compared. <br/ ><br>Timepoint: At baseline , 2 min interval till 10 minutes & then at 15 minutes interval till completion of surgery & postoperative period till patient complains of pain.