Comparison of two drugs as an adjuvant to a local anesthetic for post operative pain relief under spinal anesthesia

Not Applicable

Recruiting

• Conditions: Medical and Surgical,

• Registration Number: CTRI/2019/01/017078
• Lead Sponsor: Sri Venkateshwaraa Medical College Hospital Research Centre

Brief Summary

This is a post-graduate thesis approved by Institutional ethical committee on 28 Nov.2018. Two drugs are to be compared in this study. The study is likely to be started on 15 Jan 2019.

Detailed Description

Not available

Study Timeline

• Study Start: 2019-01-15
• Last Update Posted: 2022-10-25

Recruitment & Eligibility

• Status: Open to Recruitment
• Sex: All
• Target Recruitment: 140

Inclusion Criteria

ASA I & II Age 18 to 60 years of Both Sex.

Exclusion Criteria

• Patients with any contraindication for spinal anesthesia Patients with psychiatric illness or on any antipsychotic Medication Short stature.
• Allergic to local anesthetic Patients converted to general anesthesia.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Duration of post-operative pain relief	Assessed at every 30 minutes interval until the first dose of pain killer is given.

Secondary Outcome Measures

Name	Time	Method
Time to onset of sensory and motor block.	This will be assessed only once after spinal anesthesia. The time taken for establishment of sensory and motor block will be noted.

Trial Locations

Locations (1)

SRI VENKATESHWARAA MEDICAL COLLEGE HOSPITAL AND RESEARCH CENTRE; 🇮🇳 Pondicherry, PONDICHERRY, India

SRI VENKATESHWARAA MEDICAL COLLEGE HOSPITAL AND RESEARCH CENTRE

🇮🇳Pondicherry, PONDICHERRY, India

Roshini Devi P

Principal investigator

9566341988

roshiniog@gmail.com