Actively Recruiting

All Genders
NCT03309384

Intraoperative Monitoring to Predict Postoperative Complications After Thyroidectomy

Led by Central Hospital, Nancy, France · Updated on 2025-02-12

1000

Participants Needed

1

Research Sites

521 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this study is to evaluate the role of intraoperative continous and intermittent neuromonitoring and intraoperative parathormone (PTH) to predict postoperative nerve morbidity and hypocalcemia.

CONDITIONS

Official Title

Intraoperative Monitoring to Predict Postoperative Complications After Thyroidectomy

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients scheduled for total thyroidectomy at University Hospital of Nancy
Not Eligible

You will not qualify if you...

  • Refusal to participate

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

CHU Nancy

Vandœuvre-lès-Nancy, France, 54511

Actively Recruiting

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Research Team

B

Brunaud

CONTACT

J

Jacquel

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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