Comparison of two drugs for anaesthesia in spinal block for lower limb surgery

Not Applicable

Completed

• Conditions: Health Condition 1: S723- Fracture of shaft of femurHealth Condition 2: S822- Fracture of shaft of tibiaHealth Condition 3: S821- Fracture of upper end of tibia

• Registration Number: CTRI/2022/04/041726
• Lead Sponsor: Department of Anaesthesiology

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Completion: 2023-04-15
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 80

Inclusion Criteria

Patients with ASA physical status Grade I and II of either sex.

Patients in the age group of 18-60 years.

Posted for lower limb orthopedic surgeries under spinal anaesthesia.

Exclusion Criteria

Patients posted for emergency surgeries.

Pregnant patients.

Patients having coagulation abnormalities, platelet count <75,000, INR >1.5, or on anticoagulants.

Patients having systemic illness (severe hypovolemia, raised intracranial pressure, neuromuscular diseases, ischemic/ valvular/ congenital heart diseases, psychiatric, hematological disorder).

Patients having any absolute contraindications for spinal anesthesia.

Patient refusal to participate in study.

Any allergy to study drugs or local anaesthetic drugs.

Short stature (height <150cms), with spinal deformity.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Duration of AnalgesiaTimepoint: 4 hours postoperatively

Secondary Outcome Measures

Name	Time	Method
onset and duration of sensory block, onset and duration of motor block and hemodynamic parameters.Timepoint: Intraoperative (3-4 hours)