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Comparison of efficacy of different doses of clonidine with 0.5%hyperbaric bupivacaine in spinal anaesthesia for lower limb surgeries.

Comparative study of intra-thecal 0.5% bupivacaine with 20mcgs clonidine versus 30mcgs clonidine to assess the effectiveness of post-operative analgesia - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/09/057616
Enrollment
100
Registered
2023-09-14
Start date
Unknown
Completion date
Unknown
Last updated
2023-09-18

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

Conditions

Health Condition 1: 4- Measurement and Monitoring

Interventions

Intervention1: Different doses of clonidine: To compare the effectiveness of postoperative analgesia with 20mcgs clonidine to 0.5%hyperbaric bupivacaine intrathecally versus 30mcgs clonidine to 0.5%h

Sponsors

Acs medical college and hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient aged between 18years and 60years of age posted for infra umbilical surgeries and fit for spinal anesthesia

Exclusion criteria

Exclusion criteria: Patient refusal, ishaemic heart disease /bleeding disorders/bronchial asthma Syndromic patients Infection at lumbar site

Design outcomes

Primary

MeasureTime frame
Onset of sensory and motor blockade in patients undergoing infra umbilical surgeries Total duration of postoperative analgesia Time for first rescue analgesic Duration of 2 segment regression of sensory blockade Duration of motor blockadeTimepoint: Intraop monitoring for every 10mis for first hour followed by every 20mins for subsequent hours Postoperative monitoring every hour for 24 hours

Secondary

MeasureTime frame
Hemodynamic stabilityTimepoint: intraoperative period for every 20mins Postoperative period hourly monitoring

Countries

India

Contacts

Public ContactRama Selvam

Acs medical college and hospital

drrama87@gmail.com9566823041

Outcome results

None listed

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