Skip to content

Comparison of two local anaesthetics in spinal anaesthesia

A comparative study of 0.75% ropivacaine heavy versus 0.5% bupivacaine heavy in subarachnoid block for infra umbilical surgeries.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/04/041908
Enrollment
60
Registered
2022-04-19
Start date
Unknown
Completion date
Unknown
Last updated
2022-05-02

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: group 1 (Ropivacaine): 3.5 ml of 0.75% hyperbaric Ropivacaine will be administered in spinal anaesthesia Control Intervention1: group 2 (Bupivacaine): 3.5 ml of 0.5% hyperbaric Bupivaca

Sponsors

Sree Balaji Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA 1&2 Undergoing infra umbilical surgery under subarachnoid block Consenting to participate in the study

Exclusion criteria

Exclusion criteria: Patient refusal Allergy to local anaesthetics Local infection at the site of block Bleeding disorder Pre operative hypotension pregnancy

Design outcomes

Primary

MeasureTime frame
onset and duration of sensory blockTimepoint: The onset of sensory block at T10 will be monitored from positioning the patient after spinal anaesthesia at every 30 seconds and thereafter at every 3 minutes for the 1st 15 minutes and at every 30 minutes till it recedes to S2

Secondary

MeasureTime frame
hemodynamic disturbance and complications.Timepoint: vital parameters will be monitored from 0 minute at 3 minute interval till 1st 15 minutes, at 10 minutes interval during the surgery and at 30 minutes interval till complete recovery. fall in MAP or SBP more than 30% or heart rate below 50/min requiring pharmacological treatment will be noted and patient followed up for 24 hours to note other complications such as nausea vomiting, rashes, urinary retention if any;onset and duration of motor blockTimepoint: motor block will be monitored from 0 minute at 30 seconds interval till grade 3 block according to modified Bromage scale is achieved and at 30 minutes interval till complete regression of motor block

Countries

India

Contacts

Public ContactGayathri Ramesh

Sree Balaji medical college and hospital

docgayu@gmail.com9004645828

Outcome results

None listed

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