NCT03570021Active, not recruitingPhase 3
ESTIMation of the ABiLity of Prophylactic Central Compartment Neck Dissection to Modify Outcomes in Low-risk Differentiated Thyroid Cancer
Source: ClinicalTrials.gov · Last updated 6 Mar 2026
Brief summary (registry, in English)
Prospective randomized open phase III non-inferiority trial in cT1bT2N0 papillary thyroid carcinoma comparing: total thyroidectomy alone (experimental group) versus total thyroidectomy + Prophylactic Neck Dissection PND (reference group). Pre-registered patients will be randomized before surgery for tumors with class-6 cytology (Bethesda) or in the operating room after confirmation of malignancy by frozen section analysis for tumors with class-5 cytology.
- Status (registry)
- Active, not recruiting
- Phase (registry)
- Phase 3
- Study type
- Interventional
- Enrollment
- 352 (actual)
- First submitted
- 15 Jun 2018
- Start date
- 8 Aug 2018
- Primary completion date
- Dec 2026
- Lead sponsor
- Gustave Roussy, Cancer Campus, Grand Paris
- Diseases
- Thyroid cancer
- NCT number
- NCT03570021
What you commit to
- Study type: Interventional · Phase 3
- Participants enrolled: 352
- From 8 Aug 2018 to the primary completion date, Dec 2026
- 21 sites in 3 countries
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Metastatic neck lymph nodes or suspicious neck nodes on pre- operative ultrasound (cN1); for suspicious nodes, FNAB cytology and thyroglobulin assay on the needle washout fluid will be performed
Lab values
- Medullary thyroid carcinoma on FNAB cytology and/or with basal serum calcitonin \>50 pg/ml
- Recurrent nerve paralysis visualized on systematic pre-operative laryngoscopy and/or abnormal preoperative serum calcium
Other
- Tumors \> 40 mm (cT3) or ≤ 10 mm
- Tumors with extrathyroidal extension suspected or obvious on the pre-operative work-up or intra-operatively (cT3T4)
- Metastatic neck lymph nodes found during the thyroidectomy and confirmed with intra-operative frozen section analysis
- Preoperative or intra-operative suspicion of non-papillary thyroid carcinoma or aggressive histopathological subtype or poorly differentiated carcinoma
- Distant metastases (M1) apparent pre-operatively (found due to symptoms or fortuitously; no specific pre-operative work-up will be performed, however, in accordance with current clinical practice)
- Pregnant or breast feeding women
- Participation in another therapeutic clinical trial within one year from study entry
- Patient under guardianship or deprived of his liberty by a judicial or administrative decision or incapable of giving its consent
Who the study is looking for
- Thyroid nodule measuring 11-40 mm on ultrasound (cT1bT2)
- AND with fine-needle aspiration biopsy (FNAB) cytology in favor of "papillary thyroid carcinoma" (Type 6 according to the Bethesda classification (or BRAF mutation found on cytology analysis) (Appendix 2)
- OR with FNAB cytology "suspicious for malignancy" (Type 5 according to the Bethesda classification). In this latter case, randomization will be performed if confirmation of papillary carcinoma on intraoperative frozen section analysis
- cN0: absence of lymph nodes suspicious for malignancy on pre- operative ultrasound performed by the center's designated radiologist according to a standardized report
- Absence of a medical contra indication to performing a total thyroidectomy with or without bilateral prophylactic neck dissection of the central compartment
- Women of childbearing potential should have a negative pregnancy test (serum or urine) before any radioiodine administration. Sexually active patients must agree to use an effective method of contraception or to abstain from sexual activity during the study and for at least 6 months after last dose of radioiodine.
- Patient affiliated to a social security regimen or beneficiary of such regimen
- Patients age ≥ 18 years old, french-speaking
- Patients should understand, sign and date the written informed consent form prior to any protocol specific procedures. Patients should be able and willing to comply with study visits.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (21)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| CHU d Angers Coordinator of this site? Confirm its status | Angers | France | Unknown status |
| Institut Bergonie Coordinator of this site? Confirm its status | Bordeaux | France | Unknown status |
| Hôpital Saint-André Coordinator of this site? Confirm its status | Bordeaux | France | Unknown status |
| Groupement Hospitalier Est Coordinator of this site? Confirm its status | Bron | France | Unknown status |
| Centre François Baclesse Coordinator of this site? Confirm its status | Caen | France | Unknown status |
| Jean Perrin Coordinator of this site? Confirm its status | Clermont-Ferrand | France | Unknown status |
| Centre Georges François Leclerc Coordinator of this site? Confirm its status | Dijon | France | Unknown status |
| CH de Haguenau Coordinator of this site? Confirm its status | Haguenau | France | Unknown status |
| CHU Lille - Hôpital Claude Huriez Coordinator of this site? Confirm its status | Lille | France | Unknown status |
| CHU Nîmes Coordinator of this site? Confirm its status | Nîmes | France | Unknown status |
| CHU de Poitiers Coordinator of this site? Confirm its status | Poitiers | France | Unknown status |
| Institut Godinot Coordinator of this site? Confirm its status | Reims | France | Unknown status |
| CHU Reims Hopital Robert Debre Coordinator of this site? Confirm its status | Reims | France | Unknown status |
| Centre Henri Becquerel Coordinator of this site? Confirm its status | Rouen | France | Unknown status |
| Institut De Cancerologie Strasbourg Coordinator of this site? Confirm its status | Strasbourg | France | Unknown status |
| Institut Claudius Regaud Coordinator of this site? Confirm its status | Toulouse | France | Unknown status |
| CHU de Toulouse - Hopital Larrey Coordinator of this site? Confirm its status | Toulouse | France | Unknown status |
| CHRU Nancy - Hôpitaux de Brabois Coordinator of this site? Confirm its status | Vandœuvre-lès-Nancy | France | Unknown status |
| Gustave Roussy Coordinator of this site? Confirm its status | Villejuif | France | Unknown status |
| CHU de Pointe à Pitre Coordinator of this site? Confirm its status | Les Abymes | Guadeloupe | Unknown status |
| Clinique Saint Vincent Coordinator of this site? Confirm its status | Réunion | Réunion | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.