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Comparison of two drugs 0.5% levobupivacaine versus 0.75% ropivacaine under spinal anaesthesia in caesarean delivery for the duration of effect of pain relief and to know which drug is better for long duration od pain relief.

A randomised comparative study for the efficacy of 0.5% hyperbaric Levo bupivacaine versus 0.75% hyperbaric ropivacaine in parturients undergoing lower segment caesarean section under spinal anaesthesia - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/01/062119
Enrollment
96
Registered
2024-01-31
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O00-O9A- Pregnancy, childbirth and the puerperium Health Condition 2: O099- Supervision of high risk pregnancy, unspecified

Interventions

Intervention1: To find out which drug is better in terms of post operative analgesia in parturients undergoing LSCS under spinal anaesthesia: To find out the efficacy of 0.5% hyperbaric bupivacaine 1.

Sponsors

SMS Medical College and hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Parturients willing to participate in the study undergoing LSCS under subarachnoid block with age group of 18 to 40 years and ASA grade II

Exclusion criteria

Exclusion criteria: Parturient should not be a part of other study,non co-operative parturient,history of allergy or hypersensitivity to any drug of study,any deformity or local sepsis in spinal lumbar region,severe hypovolemia,any bleeding or coagulation abnormalities,parturients receiving tranquillisers,phenothiazines or other CNS depressants including alcohol,any major pre-existing comorbidities such as COPD,neurological,cardiovascular,metabolic,hepatic,respiratory or renal disease

Design outcomes

Primary

MeasureTime frame
To assess and compare mean time of onset of sensory and motor blockade between the study groups,level of sensory blockade at different time intervals until the highest level achieved,time duration of sensory and motor block,requirement of first rescue analgesia in post operative period between the study groups.Timepoint: 1,2,3,5,10,15,20,25,30,40,50,60 minutes—

Secondary

MeasureTime frame
To assess and compare hemodynamic variables at different time intervals such as SBP,DBP,MAP and SPO2,frequency of side effects if anyTimepoint: 1,2,3,5,10,15,20,25,30,40,50,60 minutes—

Countries

India

Contacts

Public ContactDr Sandeep Chhipa

Sawai man Singh medical college, Jaipur

drsandeepchhipa@gmail.com8505052367

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026