Actively Recruiting
Intraoperative Monitoring (Parathormone Values and Continuous Neuromonitoring) to Predict Postoperative Complications After Total Thyroidectomy
Led by Central Hospital, Nancy, France · Updated on 2025-02-12
1000
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to evaluate how intraoperative continuous and intermittent neuromonitoring, along with intraoperative parathormone (PTH) levels, can help predict nerve problems and low calcium levels after thyroid removal surgery. The study focuses on patients undergoing total thyroidectomy, assessing complications related to the parathyroid glands and laryngeal nerves. It is an observational study conducted by Central Hospital, Nancy, France, to better understand postoperative risks. During surgery, continuous neuromonitoring and measurements of parathormone levels will be collected from patients having total thyroidectomy. These intraoperative data points are used to predict postoperative complications such as nerve injury and hypocalcemia. The study does not involve any experimental treatment but follows patients prospectively to observe outcomes. Participants will be monitored for nerve issues and calcium-related problems within the first week after surgery and again one year later. Validated classifications will be used to evaluate other complications at one year. Researchers will collect data on postoperative nerve function, calcium levels, and parathyroid function to assess the predictive value of intraoperative monitoring and PTH measurements. The total participation duration includes follow-up visits up to one year after surgery.
CONDITIONS
Brief Title
Intraoperative Monitoring to Predict Postoperative Complications After Thyroidectomy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients scheduled for total thyroidectomy at University Hospital in Nancy
You will not qualify if you...
- Refusal to participate
AI-Screening
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Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - Up to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Day of surgery and up to 1 week after surgery
Participants undergo total thyroidectomy with intraoperative monitoring of parathormone values and continuous neuromonitoring.
1 visit during surgery and follow-up assessments within 1 week after thyroidectomy
Duration - Up to 1 year after surgery
Participants are monitored for postoperative complications including hypocalcemia, hypoparathyroidism, and laryngeal nerve palsy at 1 year after thyroidectomy.
1 follow-up visit at 1 year post-thyroidectomy
Trial Site Locations
Total: 1 location
1
CHU Nancy
Vandœuvre-lès-Nancy, France, 54511
Actively Recruiting
Research Team
B
Brunaud
J
Jacquel
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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