TOETVA Technique Compared With Anterior Cervical Thyroidectomy (AC) in Terms of Efficacy and Safety
NCT ID: NCT07055191
Last Updated: 2026-01-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
616 participants
INTERVENTIONAL
2025-11-07
2028-11-30
Brief Summary
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Since 2014, the Transoral Endoscopic Thyroidectomy by Vestibular Approach (TOETVA) has been developed as an alternative to these robot-assisted procedures. Because this technique offers the surgeon similar access to the anatomical structures on both sides of the trachea and makes it possible to identify the noble structures to be preserved, TOETVA is currently undergoing a more widespread use in France and worldwide and more candidates for are being offered the procedure. TOETVA reduces the need for dissection to reach the thyroid gland. Moreover, this procedure does not require any special equipment, even if robotic assistance has been used in transoral thyroidectomy.
Just like the electric light was not developed from the continuous improvement of candles, entirely new approaches are sometimes necessary in surgery. The Scientific Committee of the French Association of Endocrine Surgery is convinced that TOETVA, will become more widely used in France, even if this technique is a major departure from the standard approach. However, it is technically more demanding and must, therefore, be evaluated and supervised. This will require a safety study and a comparison with the current reference procedure, the anterior cervical thyroidectomy (AC). The investigators assume, based on our initial experience, that the use of endoscopic equipment and its magnification will allow good visualization of the noble elements (recurrent nerve and parathyroid glands) and that the complication rate of TOETVA will not be higher than that of the reference approach.
The investigators propose to evaluate, through a prospective randomized study, an innovative endocrine surgical technique that has started to be used worldwide. Although this study is in line with the objectives of an evaluation of the pertinence of care by the health authorities, it would be the first assessment of this innovative surgical technique in thyroid surgery. To our knowledge, after an extensive bibliographic search, no prospective multicenter randomized trial comparing TOETVA to AC has yet been performed, even if many cohorts of patients have been reported to have benefited from this approach6.
In this trial, any change to the quality of life will be extensively evaluated. The use of validated scores to quantify pain and quality of life will provide objective information and make it possible to determine the impact of the presence or absence of a scar.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Transoral Endoscopic Thyroidectomy by Vestibular Approach (TOETVA)
Transoral Endoscopic Thyroidectomy by Vestibular Approach
Transoral Endoscopic Thyroidectomy by Vestibular Approach
Anterior Cervical thyroidectomy (AC)
Anterior Cervical thyroidectomy
Anterior Cervical thyroidectomy
Interventions
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Transoral Endoscopic Thyroidectomy by Vestibular Approach
Transoral Endoscopic Thyroidectomy by Vestibular Approach
Anterior Cervical thyroidectomy
Anterior Cervical thyroidectomy
Eligibility Criteria
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Inclusion Criteria
* Estimated thyroid volume measured by ultrasonography of less than 60 mL
* Nodules suspected to be malignant measuring less than 4 cm
* Patient aged between 18 and 65 years old
* Patient who has benefited from an endocrinological evaluation, with a favorable opinion for TOETVA or AC Patient who understands and accepts the need for follow-up
* Patient who agrees to be included in the study and who signs the informed consent form
* Patient affiliated to a healthcare insurance plan
Exclusion Criteria
* History of cervical surgery
* Associated parathyroid surgery
* Identification of malignant lymph nodes
* Presence of a severe and evolutive life threatening pathology
* Patients with unstable psychiatric disorder, under supervision or guardianship
* Patient who does not understand French/ is unable to give consent
* Patient not affiliated to a French or European healthcare insurance
* Patient who has already been included in a trial which has a conflict of interests with the present study
* Pregnant or breast-feeding patient
* Patient incarcerated
18 Years
65 Years
ALL
No
Sponsors
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Ministry of Health, France
OTHER_GOV
University Hospital, Lille
OTHER
Responsible Party
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Locations
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AP-HP - Hôpital Avicennes
Bobigny, , France
Hôpital Franco-Britannique
Levallois-Perret, , France
CHU de Lille, Hôpital Huriez
Lille, , France
CHU Dupuytren
Limoges, , France
CHU de Nantes - Hôtel Dieu
Nantes, , France
AP-HP - Hôpital Cochin
Paris, , France
Hôpital Lyon Sud
Pierre-Bénite, , France
CHU de Poitiers
Poitiers, , France
Polyclinique de la Côte Basque Sud
Saint-Jean-de-Luz, , France
CHRU de Nancy Brabois
Vandœuvre-lès-Nancy, , France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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PHRC-21-0340
Identifier Type: OTHER_GRANT
Identifier Source: secondary_id
2022-A02301-42
Identifier Type: OTHER
Identifier Source: secondary_id
2022_0509
Identifier Type: -
Identifier Source: org_study_id
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