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Femoral Blockade and Low-dose Spinal Anesthesia in Outpatient Knee Arthroscopy

NCT02322372 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2015-02-18

No results posted yet for this study

Summary

The investigators of the current study aimed to evaluate the effect of spinal anesthesia with low dose bupivacaine combined with femoral blockade on duration of anesthesia and time of first analgesic requirement during postoperative period

Conditions

  • Meniscus Lesion

Interventions

DRUG

Femoral blockade

Spinal anesthesia with heavy bupivacaine combined with femoral blockade with bupivacaine

DRUG

Intrathecal anesthesia

Spinal anesthesia with heavy bupivacaine

Sponsors & Collaborators

  • Ankara University

    lead OTHER

Principal Investigators

  • Ramazan Akmese, Specialist · Ankara University Faculty of Medicine

  • Fatma Ozkan, Assistant · Ankara University Faculty of Medicine

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
25 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-07-31
Primary Completion
2014-12-31
Completion
2014-12-31

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 NCT02322372 on ClinicalTrials.gov