Study of Transaxillary Robotic Thyroidectomy Versus Standard Open Thyroidectomy: Prospective, Comparative Single-Center Study

NCT ID: NCT06693258

Last Updated: 2026-01-06

Study Results

Results pending

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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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-11-25

Study Completion Date

2026-07-31

Brief Summary

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The aim of our study is to evaluate the two surgical approaches, standard thyroidectomy and robotic thyroidectomy, in terms of postoperative pain management, scar quality, quality of life, as well as the occurrence of postoperative complications (hypocalcemia, compressive cervical hematoma and nerve stimulation)

Detailed Description

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Conditions

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Carpal Tunnel Surgery

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Prospective, Comparative, Monocentric Study
Primary Study Purpose

OTHER

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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Experimental group

thyroidectomy by robotic surgery via axillary approach

Group Type EXPERIMENTAL

thyroidectomy by robotic surgery via axillary approach

Intervention Type PROCEDURE

thyroidectomy

Control group

thyroidectomy by standard conventional surgery

Group Type ACTIVE_COMPARATOR

thyroidectomy by standard conventional surgery

Intervention Type PROCEDURE

thyroidectomy by standard conventional surgery

Interventions

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thyroidectomy by robotic surgery via axillary approach

thyroidectomy

Intervention Type PROCEDURE

thyroidectomy by standard conventional surgery

thyroidectomy by standard conventional surgery

Intervention Type PROCEDURE

Eligibility Criteria

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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.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Clinique Bizet

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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clinique Bizet

Paris, , France

Site Status RECRUITING

Countries

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France

Facility Contacts

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bouchra benkessou, chef de projet

Role: primary

07 64 48 60 16

Other Identifiers

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2024-A01697-40

Identifier Type: -

Identifier Source: org_study_id

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