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Comparison of maternal hemodynamic parameters with the time taken and level of sensory and motor blockade

A comparative clinical study between equivolume dosage of 0.5 % hyperbaric Bupivacaine versus 0.5 % hyperbaric Bupivacaine with fentanyl intrathecally in a parturient posted for elective cesarean section. - Nil

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/03/063521
Enrollment
60
Registered
2024-03-04
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-01

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Bupivacaine: Single dose, Subarachnoid block ,Bupivacaine heavy 0.5 % with Inj fentanyl 15 mcg Control Intervention1: Bupivacaine heavy 0.5 %: Single dose,Subarachnoid block, Bupivacain

Sponsors

Dr Jumana Afrin U
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Parturients willing to give informed and written consent. 2. Singleton pregnant mothers schedules for elective LSCS done under Sub Arachnoid block. 3. Parturients belonging to ASA ll 4. Height of parturients to be 150 to 170 cms.

Exclusion criteria

Exclusion criteria: 1. Parturient refusal. 2. ASA lll and above 3. Parturients hypersensitive to study drug. 4. Parturients with significant coagulopathies and other contra indications for spinal anaesthesia. 5. Parturients with pregnancy induced Hypertension. 6. Parturients with history of significant systemic disorders (cardiovascular, respiratory or central nervous system) 7. Parturients with fetal anomalies and twin gestation. 8. Parturients with oligohydraminios. 9. Precious pregnancy.

Design outcomes

Primary

MeasureTime frame
-Maternal heart rate, blood pressure, mean arterial pressure, oxygen saturation - level of sensory and motor blockade achieved time taken to attain maximum blockade - maximum blockade achievedTimepoint: Assessed preoperatively, at 2 minutes interval for first 10 minutes after sub arachnoid block, every 5 minutes for the next 20 minutes and every 10 minutes thereafter for one hour.

Secondary

MeasureTime frame
Intra & post operative adverse effects like itching, nausea, vomitingTimepoint: During procedure, 1 hour after procedure

Countries

India

Contacts

Public ContactDr Yoganarasimha N

BGS Global Institute of Medical Sciences

Dr.jumanaafrin@gmail.com9036129794

Outcome results

None listed

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