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Comparative Study on the Effectiveness of Butorphanol vs Tramadol in Managing Post-Spinal Anaesthesia Shivering

Comparative study on effectiveness of Butorphanol VS Tramadol on post spinal anaesthesia shivering - NIL

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/12/078088
Enrollment
60
Registered
2024-12-13
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: Inj BUTORPHANOL: Inj BUTORPHANOL given intravenously in patients who develop shivering over a period of 10 mins.The attending anesthesiologist recorded the time in minutes at which shiv

Sponsors

Dr Ritin Saxena
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: ASA grade 1 or 2 fit patients. Patient undergooing surgeries under spinal anaesthesia. Haemodynamically stable patients with all routine investigations Within normal limits without any other comorbidities. patients who are not on any cardiac related drugs. availability of written informed consent from concerned patient

Exclusion criteria

Exclusion criteria: Patients not willing to get enrolled in this study. Patients with ASA physical status III or more. Patients below 18 years and above 60 years of age. Patients posted for emergency procedures. Patients with uncontrolled systemic disorders like diabetes mellitus, heart disease, chronic hypertension, pulmonary disorders, etc. Patients with spine deformities or local skin interactions overlying the lumbar vertebral region. Patients with bleeding or coagulation disorders. Patients with known allergies to the study drugs.

Design outcomes

Primary

MeasureTime frame
Efficacy and haemodynamic effects of Butorphanol and Tramadol, for the control of Post-Spinal Anaesthesia ShiveringTimepoint: After administering Sub arachnoid block; 0, 1, 2, 5, 10, 15 and 30 minutes after administering the test drug.

Secondary

MeasureTime frame
Adverse effects of Butorphanol & Tramadol in sub arachnnoid block.Timepoint: After administering Sub arachnoid block.

Countries

India

Contacts

Public ContactDr Subha Teresa Jose Vazhakalayil

DR. D.Y.PATIL MEDICAL COLLEGE, HOSPITAL AND RESEARCH CENTRE, PIMPRI, PUNE

dr.subhajose@gmail.com9558224077

Outcome results

None listed

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