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Comparison of ropivacaine and levobupivacaine for spinal anaesthesia in patients of caesarian section

Comparative evaluvation of spinal anaesthesia with hyperbaric solution of levobupivacaine and ropivacaine for caesarean section Randomized double-blind controlled study - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/12/078329
Enrollment
80
Registered
2024-12-19
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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: Spinal anaesthesia with either 2ml of 0.5% hyperbaric levobupivacaine or 0.75% hyperbaric ropivacaine: Spinal anaesthesia is given in the L3-L4 subarachnoid space with a 25G spinal need

Sponsors

Department of Anesthesia Medical college Dungarpur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • ASA physical status I and II, • Age between 18-35 years • At Term, Elective caesarean Section • Valid informed consent • height ranging between 150 – 170 cms • weight ranging between 50 – 90 kg.

Exclusion criteria

Exclusion criteria: •Pregnant patients having coexisting systemic disorders like neuromuscular diseases, neuronal degenerative disorder, seizure disorder, bleeding and haematological disorders, Cardiac disorders, Diabetes mellitus or gestational diabetes. • Pregnant women with hepatic and renal disorders, severe Anaemia • Eclampsia, placenta previa, abruptio placenta • Parturient in active labour, Twin/ complicated pregnancy • Spinal deformities, poliomyelitis short stature

Design outcomes

Primary

MeasureTime frame
onset of the sensory blockTimepoint: onset of the sensory block upto 10 minutes after spinal anesthesia

Secondary

MeasureTime frame
Time to peak sensory block. Duration of the sensory block Time to complete motor block. Duration of the motor block Intraoperative Hemodynamic. Complications.(If any ) Timepoint: Duration of sensory block

Countries

India

Contacts

Public ContactDr Mamta Damor

Govt. Medical college dungarpur

vineeta7goda@gmail.com8441896796

Outcome results

None listed

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