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Comparing The Efficiency of Oral Clonidine, Tramadol and Ondansteron given 1 hour prior to surgery as premedication to prevent Shivering after Spinal Anaesthesia

A Study to Compare The Efficacy of Oral Clonidine, Tramadol and Ondansteron as Premedication for Prevention of Post Spinal Shivering - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/07/071270
Enrollment
96
Registered
2024-07-25
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Health Condition 1: M959- Acquired deformity of musculoskeletal system, unspecified

Interventions

Intervention1: Tab. Clonidine 100 mcg: Given 1 hour before surgery with sips of water Control Intervention1: Tab. Tramadol 50mg: Given 1 hour before surgery with sips of water Control Intervention2:

Sponsors

Sapthagiri Institute of Medical Sciences And Research Centre
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA grade 1 and 2

Exclusion criteria

Exclusion criteria: Patients not willing to participate in the study. Participants who had history of drug or alcohol abuse and/or those who were on beta blockers, vasodilators, gonadotropins, tramadol, clonidine, ondansetron or pregabalin before surgery. pregnant women.

Design outcomes

Primary

MeasureTime frame
To compare the efficacy between oral clonidine, tramadol and ondansetron as premedication in prevention of shiveringTimepoint: 15, 30, 45, 60, 75, 90, 120 minutes

Secondary

MeasureTime frame
1. To evaluate hemodynamic changes 2. To assess side effects if any caused by oral clonidine, tramadol and ondansetronTimepoint: 15, 30, 45, 60, 75, 90, 120 minutes

Countries

India

Contacts

Public ContactDr Shreyavathi R

Sapthagiri Institute of Medical Sciences and Research Centre

shreyamurthy8993@gmail.com9880588325

Outcome results

None listed

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