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Intraoperative Neuromonitoring of the Recurrent Laryngeal Nerve Versus Neurostimulation

NCT01163045 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 250

Last updated 2010-07-15

No results posted yet for this study

Summary

The purpose of this study is to evaluate if intraoperative neuromonitoring associated to neurostimulation of recurrent laryngeal nerve reduce the rate of recurrent laryngeal palsy respect to neurostimulation alone.

Conditions

  • Thyroidectomy

Interventions

PROCEDURE

thyroidectomy

total thyroidectomy and lobectomy

Sponsors & Collaborators

  • University of Bologna

    lead OTHER

Principal Investigators

  • Ottavio O Cavicchi, MD · ENT Clinic Ploiclinico S.Orsola-Malpighi Bologna Italy

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
84 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-01-31
Primary Completion
2009-02-28
Completion
2010-01-31

Countries

  • Italy

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 NCT01163045 on ClinicalTrials.gov