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Addition of Lidocaine to Levobupivacaine Reduces Intrathecal Block Duration

NCT01675895 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2012-12-18

No results posted yet for this study

Summary

The main objective was to test the hypothesis that adding lidocaine to hyperbaric levobupivacaine could change the duration of levobupivacaine spinal block.

Conditions

  • Benign Prostate Hyperplasia

Interventions

DRUG

Levobupivacaine lidocaine spinal anesthesia

Spinal anesthesia

DRUG

levobupivacaine Spinal anesthesia

spinal anesthesia

Sponsors & Collaborators

  • Diskapi Teaching and Research Hospital

    lead OTHER

Principal Investigators

  • Taylan Akkaya, MD · Ankara Diskapi Yildirim Beyazit Teaching and Research Hospital, Turkey.

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
40 Years
Max Age
80 Years
Sex
MALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-07-31
Primary Completion
2011-07-31
Completion
2011-07-31

Countries

  • Turkey (Türkiye)

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 NCT01675895 on ClinicalTrials.gov