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Comparison of 3 anaesthesia drugs bupivacaine levobupivacaine and ropivacaine given through space in spinal cord for pain relief in short gynaecological surgeries

Comparative study of bupivacaine zero point five percent levobupivacaine zero point five percent and ropivacaine zero point seven five percent in spinal anaesthesia for daycare gynaecological procedures - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/03/107046
Enrollment
75
Registered
2026-03-30
Start date
Unknown
Completion date
Unknown
Last updated
2026-04-27

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

Conditions

Health Condition 1: 8- Other Procedures

Interventions

Intervention1: Spinal anaesthesia: Subarachnoid block will be done under strict aseptic precautions with patient in left lateral position using twenty five G quinckespinal needle at L three L four int

Sponsors

Dr Jini S
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Asa status of one and two Height more than one forty five centimetres Written informed consent Posted for elective gynaecological surgeries

Exclusion criteria

Exclusion criteria: History of bleeding diathesis and coagulopathy Patient refusal and coagulopathy History of allergy to local anaesthetics Spinal deformities or neurological disorders Infection at site of injection History of clinically relevant respiratory cardiac hepatic disorders

Design outcomes

Primary

MeasureTime frame
To compare efficacy of zero point five percent hyperbaric bupivacaine zero point five percent hyperbaric levobupivacaine and zero point seven five percent hyperbaric ropivacaine for spinal anaesthesia in daycare gynaecological surgeries with respect to duration of sensory and motor blockTimepoint: baseline immediately after injection two minutes five minutes ten minutess fifteen minutes twenty minutes thirty minutes sixty minutes ninety miutes one hundred and twenty minutes

Secondary

MeasureTime frame
HAEMODYNAMIC CHANGESTimepoint: ;SURGEON SATISFACTIONTimepoint: ;PATIENT SATISFACTIONTimepoint: ;SIDE EFFECTS IF ANYTimepoint: ;Onset of sensory & motor blockTimepoint: baseline immediately after injection two minutes five minutes ten minutess fifteen minutes twenty minutes thirty minutes sixty minutes ninety miutes one hundred & twenty minutes

Countries

India

Contacts

Public ContactDr Shruti Hiremath

Shimoga institute of medical sciences

drshrutihiremath@gmail.com8197724745

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: May 1, 2026