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Bilateral Superficial Cervical Block for Thyroidectomy

NCT01171885 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2010-07-29

No results posted yet for this study

Summary

The objective of this study is to compare the postoperative analgesia afforded by bilateral superficial cervical block using different concentrations of local anesthetic (ropivacaine) in patients undergoing total thyroidectomy for the mini-incision technique, performed by the same surgical team.

Conditions

  • Cervical Pain

Interventions

DRUG

0.9% saline

20 ml of 0.9% saline

DRUG

Ropivacaine

20 ml of Ropivacaine 0.25%.

DRUG

Ropivacaine

20 ml of Ropivacaine 0.5%.

Sponsors & Collaborators

  • Federal University of Minas Gerais

    collaborator OTHER

  • Lifecenter Hospital

    lead OTHER

Principal Investigators

  • Carlos Leonardo A Boni, MD · Federal University of Minas Gerais

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-07-31
Primary Completion
2011-12-31
Completion
2011-12-31

Countries

  • Brazil

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 NCT01171885 on ClinicalTrials.gov