A Clinical to compare the effects of two drugs hyperbaric Bupivacaine and hyperbaric Ropivacaine in caesarean section under Spinal Anaesthesia.
Not Applicable
- Conditions
- Health Condition 1: 1- Obstetrics
- Registration Number
- CTRI/2023/03/051045
- Lead Sponsor
- Dr Millo Tama
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA I or ASA II
term Pregnant woman
Exclusion Criteria
a.History of allergy to study drugs
b.Bleeding disorder-platelet count <50,000/micro litre, prothrombin time >14 sec International normalised ratio(INR)- >1.5
c.Local site infection
d.Cardiac, respiratory diseases and kidney disorder, neurological deficit
e.Spinal deformity
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.The block characteristics <br/ ><br>2.regression of the blockade <br/ ><br>3.side effects (if any) <br/ ><br>4.hemodynamic changesTimepoint: outcome will be assesed after the administration of local anaesthetic at predetermined interval and data will be assesed at the end of the year.
- Secondary Outcome Measures
Name Time Method 1.BP,PR, <br/ ><br>2.Onset sensory block 10 <br/ ><br>3.Time to attain T4-6 <br/ ><br>4.Time to two segment regression <br/ ><br>5.Total duration Sensory block <br/ ><br>6.Onset Motor block <br/ ><br>7.Time to Complete Motor block <br/ ><br>8.Time to rescue Analgesia <br/ ><br>9.Side effects if anyTimepoint: 1.0,10,15,20,30,40,50,60(mt) <br/ ><br>2.Assesed and recorded after spinal every 2 minutes till 10 Sensory block <br/ ><br>3.Assesed and recorded after spinal every 2 minute till T4-6 level reached <br/ ><br>7.Assesed and recorded as per bromage scale till complete block 2 minutes after spinal <br/ ><br>8.Noted as per symptoms of patient <br/ ><br>9.Note time if any side effects as per symptoms if any