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Comparing intrathecal levobupivacaine with bupivacaine for infraumbilical surgeries

Comparison of intrathecal levobupivacaine with bupivacaine in adult patients undergoing infraumbilical surgeries under neuraxial anaesthesia - NIL

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/01/061492
Enrollment
82
Registered
2024-01-15
Start date
Unknown
Completion date
Unknown
Last updated
2024-01-22

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 Health Condition 2: O- Medical and Surgical Health Condition 3: O- Medical and Surgical

Interventions

Intervention1: Neuraxial Block: comparison between hyperbaric levobupivacaine and levobupivacaine with respect to duration of anaesthesia,motor blockade,analgesia,incidence of intraoperative hypotens

Sponsors

Maj Dr Lalita Sharma
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA physical status I to II Age 18-50yrs Elective Surgeries Height >150 cms

Exclusion criteria

Exclusion criteria: History of severe headache and migraine. Failure to achieve desired motor or sensory blockade Neurological deficit Emergency surgeries Increased intracranial pressure Coagulation and bleeding disorders Infection at the site of needle insertion Spine deformities Spinal Anaesthesia converted to General Anaesthesia

Design outcomes

Primary

MeasureTime frame
Comparison of duration of anaesthesia. Timepoint: Outcome of the study will be observed after the end of surgery and patients recover to preoperative condition.

Secondary

MeasureTime frame
Total duration of motor block. Total duration of analgesia. Incidence of hypotension and bradycardia. Timepoint: every min till 10 min, at the end of surgery and every 30 min thereafter till complete recovery achieved

Countries

India

Contacts

Public ContactLt Col Dr Abraham L C

Command Hospital EC Kolkata

deepakdwivedi739@gmail.com8195915566

Outcome results

None listed

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