Health Condition 1: 1- Obstetrics
Conditions
Interventions
Intervention1: Hyperbaric Ropivacaine: Study participants will be randomised into two groups.Intervention group will receive the 2 ml of 0.5% of hyperbaric intrathecally for spinal anaesthesia.
Contro
Sponsors
Dr Millo Tama
Eligibility
Inclusion criteria
Inclusion criteria: ASA I or ASA II term Pregnant woman
Exclusion criteria
Exclusion criteria: a. History of allergy to study drugs b. Bleeding disorder-platelet count 14 sec International normalised ratio(INR)- >1.5 c. Local site infection d. Cardiac, respiratory diseases and kidney disorder, neurological deficit e. Spinal deformity
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1.The block characteristics 2.regression of the blockade 3.side effects (if any) 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
| Measure | Time frame |
|---|---|
| 1.BP,PR, 2.Onset sensory block 10 3.Time to attain T4-6 4.Time to two segment regression 5.Total duration Sensory block 6.Onset Motor block 7.Time to Complete Motor block 8.Time to rescue Analgesia 9.Side effects if anyTimepoint: 1.0,10,15,20,30,40,50,60(mt) 2.Assesed and recorded after spinal every 2 minutes till 10 Sensory block 3.Assesed and recorded after spinal every 2 minute till T4-6 level reached 7.Assesed and recorded as per bromage scale till complete block 2 minutes after spinal 8.Noted as per symptoms of patient 9.Note time if any side effects as per symptoms if any | — |
Countries
India
Contacts
Public ContactDr A Jack Meitei
Manipur University
Outcome results
None listed