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Spinal Anaesthesia With Levobupivacaine 0.5% and Ropivacaine 0.75% for Lower Limb Orthopaedic Surgery

NCT02201784 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2015-01-21

Study results available
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Summary

The purpose of this study is to compare the effects of two intrathecally administered drugs:0.5% levobupivacaine and0.75%Ropivacaine in spinal anesthesia

Conditions

  • Lower Limb Surgery

Interventions

DRUG

Levobupivacaine

Comparison of Equipotent doses

DRUG

Ropivacaine

Comparison of equipotent doses

Sponsors & Collaborators

  • Aligarh Muslim University

    lead OTHER

Principal Investigators

  • Manazir Athar, M.D · Jawaharlal Nehru Medical College, AMU,Aligarh, India

  • Syed Moied Ahmed, PhD, M.D · Jawaharlal Nehru Medical College, AMU, Aligarh, India

  • Masood H Siddiqi, M.S · Jawaharlal Nehru Medical College, AMU, Aligarh, India

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-12-31
Primary Completion
2014-01-31
Completion
2014-01-31

Countries

  • India

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02201784 on ClinicalTrials.gov