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Durind operation are giving numbness causing drugs [BUPIVACAINE or levobupivacaine] in the backbone and comparing the effects in delivering the baby by opening the uterus

Comparing clinical efficacy of intrathecal hyperbaric bupivacaine and levobupivacaine in subarachnoid block for cesarean section Randomised double blinded study

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/01/049231
Enrollment
120
Registered
2023-01-25
Start date
Unknown
Completion date
Unknown
Last updated
2023-02-06

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

Conditions

Health Condition 1: O998- Other specified diseases and conditions complicating pregnancy, childbirth and the puerperium

Interventions

Intervention1: Levobupivacaine: Dose 2 ml of hyperbaric Levobupivacaine contains 10 mg, Route Intrathecal , Duration of intervention over 5 minutes, Frequency once. Control Intervention1: Bupivacaine

Sponsors

Gowri N
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA grade 2

Exclusion criteria

Exclusion criteria: Height less than 145cm Patient with sensory or motor neuropathy Musculoskeletal disorder Coagulation abnormalities Allergic reaction to local anaesthetic drugs Local infection Patient wo are no willing to participate in study

Design outcomes

Primary

MeasureTime frame
To study and compare onset and duration of motor and sensory block Time to regressionTimepoint: Maximum 3 hours

Secondary

MeasureTime frame
To evaluate intraoperative and postoperative hemodynamic changesTimepoint: Blood pressure,Heart rate,Respiratory rate,saturation noted before giving spinal and every minute up to 10 minutes, every 2 minute for next 10 minutes, every 5 minutes for next 25 minutes.

Countries

India

Contacts

Public ContactGowri N

Sks hospital and postgraduate medical institute

gprabu_mmc@yahoo.co.in9884469456

Outcome results

None listed

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