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Immediate Postoperative Course of Patients With Mini Video Assisted Total Thyroidectomy (miVAT) Versus Classic Total Thyroidectomy (cTT)

NCT00692835 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2012-10-02

No results posted yet for this study

Summary

Protocol Synopsis

* Protocol title: Immediate postoperative course of patients with mini Video Assisted Thyroidectomy (miVAT) versus classic Thyroidectomy (cTT)
* Purpose: Comparison of the immediate postoperative course and complications of the patients using the two techniques
* Design: Prospective, single-center randomized study
* Patient Population: Male or female subjects 18 years of age or older with nodular goiter who are scheduled for total thyroidectomy (miVAT or T)
* No. of Subjects: 100 patients divided into two groups, estimated up to 1 year to enroll
* Duration of Treatment: During the operation
* Duration of Follow-up: Follow-up will be performed daily while hospitalized, and by phone till the 7th postoperative day
* Endpoints: To evaluate the safety and cost-effectiveness of each technique

Conditions

  • Goiter

Interventions

PROCEDURE

Total Thyroidectomy (Mini Video Assisted Thyroidectomy)

Immediate postoperative course of patients with Thyroidectomy

PROCEDURE

Total Thyroidectomy (Classic Thyroidectomy)

Immediate postoperative course of patients with Thyroidectomy

Sponsors & Collaborators

  • AHEPA University Hospital

    collaborator OTHER

  • Aristotle University Of Thessaloniki

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-05-31
Primary Completion
2009-12-31
Completion
2012-09-30

Countries

  • Greece

Study Locations

More Related Trials

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 NCT00692835 on ClinicalTrials.gov