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Concentration-Volume Relationship in Infraclavicular Block

NCT02820688 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 81

Last updated 2017-01-05

No results posted yet for this study

Summary

This prospective, randomized, double blind study aims to determine the optimal volume for adequate sensorial and motor blockade following an infraclavicular block. Patients will be randomized into three groups. Using a constant dose of local anesthetics (45mg bupivacaine 180mg prilocaine), different volumes will be used in each of the groups (First group; 18mL, second group; 27mL, third group; 36mL). Onset, duration and quality of sensory and motor block will be compared for patients between groups

Conditions

  • Brachial Plexus Blockade

Interventions

DRUG

Bupivacaine 0.25%

DRUG

Prilocaine 1%

PROCEDURE

Infraclavicular Nerve Block

Ultrasound guided infraclavicular nerve block

DRUG

Bupivacaine 0.167%

DRUG

Bupivacaine 0.125%

DRUG

Prilocaine 0.66%

DRUG

Prilocaine 0.5%

DEVICE

Ultrasound

All nerve blocks will be performed with ultrasound guidance

Sponsors & Collaborators

  • Bozyaka Training and Research Hospital

    lead OTHER

Principal Investigators

  • Zeki T Tekgul, MD · Izmir Bozyaka Training and Research Hospital

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-06-30
Primary Completion
2016-10-31
Completion
2016-10-31

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 NCT02820688 on ClinicalTrials.gov