Comparing robotic and standard thyroid surgery techniques
A Comparative Study of Transaxillary Robotic Thyroidectomy Versus Standard Open Thyroidectomy
NA · Clinique Bizet · NCT06693258
This study is testing whether robotic thyroid surgery done through the armpit is better than traditional surgery in terms of pain, scarring, and recovery for patients.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 100 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Clinique Bizet (other) |
| Locations | 1 site (Paris) |
| Trial ID | NCT06693258 on ClinicalTrials.gov |
What this trial studies
This study evaluates the effectiveness of two surgical approaches for thyroidectomy: the traditional open method and a robotic technique performed through the axillary approach. It focuses on postoperative pain management, scar quality, quality of life, and the incidence of complications such as hypocalcemia and hematoma. The study aims to provide insights into which method offers better outcomes for patients undergoing thyroid surgery.
Who should consider this trial
Good fit: Ideal candidates are adults over 20 years old who are scheduled for a thyroidectomy and meet specific health criteria.
Not a fit: Patients under 20 years of age or those with significant underlying health issues may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved surgical outcomes and recovery experiences for patients undergoing thyroidectomy.
How similar studies have performed: Previous studies have shown promising results with robotic surgical techniques, suggesting potential benefits over traditional methods.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Subject aged over 20 years * Referred for a thyroidectomy (total or partial) * Absence of participation in another clinical study * Subject affiliated to a social security scheme or beneficiary of such a scheme * Accepts the completion of the various study questionnaires Exclusion Criteria: * Patient under 20 years of age. * Patients who have undergone combined radical cervical lymph node dissection * Patient with a postoperative wound problem * Patient with an underlying systemic disease that may influence the wound healing process * Unable to undergo medical follow-up for the study.
Where this trial is running
Paris
- clinique Bizet — Paris, France (RECRUITING)
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
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