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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

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
NameTimeMethod
Duration of post-operative pain reliefAssessed at every 30 minutes interval until the first dose of pain killer is given.
Secondary Outcome Measures
NameTimeMethod
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

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