Papillary Thyroid CancerNCT07659717
Frozen Section-Guided Selective Ipsilateral Central Neck Dissection in Bethesda V-VI Thyroid Nodules
An observational study of Papillary Thyroid Cancer and Lymph Node Metastasis, run by Eleonora Lori, MD at 1 site in Italy.
Trial summary
The goal of this observational pilot cohort study is to evaluate the feasibility and clinical implications of frozen section analysis-guided selective ipsilateral central neck dissection in adult patients undergoing primary thyroid surgery for Bethesda V-VI thyroid nodules with a clinically node-negative neck. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Papillary Thyroid Cancer, Lymph Node Metastasis
- What is being tested?
- Frozen section analysis (FSA)
- Type of treatment
- Surgery or procedure
- How many people
- 66 participants
- Where
- 1 siteItaly
- Study dates
- 9 Jan 2023to 19 Sep 2025
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: The study population includes consecutive adult patients treated in a tertiary referral endocrine surgery unit who underwent primary thyroid surgery for cytologically suspicious or malignant thyroid nodules. Eligible patients had Bethesda V or VI thyroid cytology, a solitary low-risk thyroid nodule smaller than 2.5 cm, and a clinically node-negative neck documented by preoperative cervical ultrasound. All patients were managed according to institutional surgical protocols and had prospectively collected clinical, surgical, and histopathological data available for analysis.
Who may be able to join
- age 18 years or older.
- Adult patients undergoing primary thyroid surgery.
- Preoperative thyroid cytology classified as Bethesda V or Bethesda VI according to the Bethesda System for Reporting Thyroid Cytopathology.
- Presence of a solitary thyroid nodule.
- Maximum nodule diameter less than 2.5 cm.
- Low-risk thyroid nodule according to clinical, cytological, and ultrasound criteria.
Show all 10Show fewer
- Clinically node-negative neck, documented by preoperative cervical ultrasound.
- Availability of complete histopathological report for the thyroid specimen.
- Availability of complete histopathological report for central compartment lymph nodes, when removed.
- Written informed consent for surgery and for the use of clinical and pathological data for research purposes.
Who cannot join
- Age younger than 18 years.
- Previous thyroid or neck surgery, including completion thyroidectomy or secondary lymph node dissection
- Known cervical lymph node metastases or distant metastases at the time of surgery.
- Thyroid nodule measuring 2.5 cm or more in maximum diameter.
- Incomplete clinical and pathological data relevant to the study endpoints.
Trial locations and contacts
1 site in 1 country.
Italy1 site
Policlinico "P. Giaccone" University of Palermo
Palermo, Sicily, 90127
About this study
Official title: Frozen Section-Guided Selective Ipsilateral Central Neck Dissection in Bethesda V-VI Thyroid Nodules: A Pilot Cohort Study Informing Surgical Extent
The goal of this observational pilot cohort study is to evaluate the feasibility and clinical implications of frozen section analysis-guided selective ipsilateral central neck dissection in adult patients undergoing primary thyroid surgery for Bethesda V-VI thyroid nodules with a clinically node-negative neck.
The main questions it aims to answer are:
Read more
- Can intraoperative frozen section analysis of ipsilateral level VI lymph nodes meaningfully inform real-time surgical decision-making?
- Can this strategy support tailored escalation or de-escalation of central compartment surgery while minimizing unnecessary bilateral central neck dissection and its associated morbidity? Researchers will compare patients managed with ipsilateral central neck dissection and intraoperative frozen section analysis with patients managed without frozen section analysis, in order to evaluate differences in treatment adequacy, surgical decision-making, and pathological nodal assessment.
Participants will undergo primary thyroid surgery according to institutional practice. In patients managed with the frozen section analysis-guided strategy, one or more ipsilateral level VI lymph nodes will be removed during surgery and examined intraoperatively. The result of frozen section analysis may be used to guide the extent of central compartment surgery and the overall surgical strategy.
Read the detailed description
This observational retrospective cohort study was conducted in a tertiary referral endocrine surgery unit and was based on prospectively collected institutional data. The study included consecutive adult patients undergoing primary thyroid surgery for cytologically suspicious or malignant thyroid nodules, classified as Bethesda V or VI according to the Bethesda System for Reporting Thyroid Cytopathology.
The study was designed to evaluate whether an intraoperative strategy based on ipsilateral central neck dissection (ipsiCND) with frozen section analysis (FSA) could improve the adequacy of surgical treatment in selected patients with low-risk thyroid cancer, potentially reducing both overtreatment and undertreatment. The institutional protocol incorporating ipsiCND-FSA was introduced in September 2023. Patients treated before implementation of this protocol generally underwent total thyroidectomy according to the standard institutional practice in place at that time. After implementation of the protocol, hemithyroidectomy combined with ipsilateral central neck lymph node sampling and intraoperative frozen section analysis was systematically proposed as the preferred surgical strategy in appropriately selected patients. Total thyroidectomy remained an option for patients who declined the conservative approach after counselling regarding the malignant or suspicious nature of the thyroid nodule and the available surgical alternatives.
Eligible patients were adults aged 18 years or older with a solitary thyroid nodule measuring less than 2.5 cm in maximum diameter, classified as Bethesda V or VI on preoperative cytology, with a clinically node-negative neck documented by preoperative cervical ultrasound. Patients were considered only if they underwent primary thyroid surgery and had complete histopathological data available for the thyroid specimen and, when removed, central compartment lymph nodes. Patients with previous thyroid or neck surgery, known distant metastases at the time of surgery, incomplete clinical or pathological data relevant to the study endpoints, or reoperations such as completion thyroidectomy or secondary lymph node dissection were excluded.
All patients received detailed preoperative counselling and provided written informed consent before surgery. The information provided included the planned procedure, the possible need for intraoperative modification of the surgical strategy according to real-time findings and frozen section results, and the potential risks and benefits of the available surgical options. Patients also consented to the inclusion of their clinical and pathological data in the institutional database and to their use for research purposes. The study was conducted in accordance with the principles of the Declaration of Helsinki, followed good clinical practice standards, and was approved by the local Ethics Committee under protocol PA-1-RETRO-2026-TBD. Reporting was planned in accordance with the STROCCS recommendations for observational studies.
All surgical procedures were performed or supervised by experienced endocrine surgeons. Intraoperative nerve monitoring was routinely used in all cases as part of the standard institutional practice. The extent of thyroid surgery, either total thyroidectomy or lobectomy/isthmectomy, and the strategy for management of the central neck compartment were planned preoperatively according to cytological diagnosis, imaging findings, clinical risk profile, and institutional practice. In patients managed according to the ipsiCND-FSA protocol, the operative plan could be modified intraoperatively on the basis of frozen section findings.
Patients were stratified according to intraoperative management of the central compartment. In the FSA group, one or more ipsilateral level VI lymph nodes were removed during hemithyroidectomy and immediately submitted for frozen section analysis. Lymph nodes were processed using standard cryostat techniques, stained with hematoxylin and eosin, and evaluated intraoperatively by an experienced pathologist. The intraoperative nodal status was reported as positive or negative for metastatic disease. Definitive paraffin-embedded histopathology served as the reference standard for final assessment. In the non-FSA group, no intraoperative frozen section analysis of central compartment lymph nodes was performed. In this cohort, patients underwent total thyroidectomy, reflecting the inability to obtain sufficiently reliable preoperative risk stratification according to the standard approach used before implementation of the new protocol.
The primary objective of the study was to assess treatment adequacy. Treatment adequacy was defined as the concordance between the surgical procedure actually performed and the minimum surgical treatment considered necessary to achieve appropriate locoregional disease control on the basis of final histopathological findings. The minimum necessary extent of surgery was determined retrospectively, with particular attention to definitive tumor characteristics, including tumor focality and laterality, extrathyroidal extension, vascular invasion, aggressive histological variants, and nodal involvement.
Overtreatment was defined as performance of total thyroidectomy in patients who were ultimately found to have a solitary unilateral carcinoma without microscopic or macroscopic extrathyroidal extension, vascular invasion, or aggressive histological variants. Undertreatment was defined as an insufficient extent of surgery in the presence of adverse pathological features requiring a more comprehensive oncological procedure. These definitions were applied irrespective of study group allocation. For comparative analyses, overtreatment and undertreatment were also combined into a composite endpoint of surgical mis-treatment.
Secondary objectives included evaluation of the diagnostic performance of frozen section analysis for detecting central compartment lymph node metastases. Diagnostic performance was assessed by calculating sensitivity, specificity, positive predictive value, negative predictive value, overall accuracy, and the area under the receiver operating characteristic curve, using definitive histopathology as the reference standard. Additional secondary outcomes included postoperative complications and length of hospital stay. Postoperative complications included major complications such as recurrent laryngeal nerve injury, hypoparathyroidism, postoperative hemorrhage, and minor complications such as seroma, hematoma, and wound infection.
Clinical, surgical, pathological, and postoperative data were extracted from the prospectively maintained institutional database and cross-checked against source documents, including operative reports, pathology reports, ultrasound reports, discharge summaries, and postoperative follow-up records. Data quality was supported by predefined data fields, standardized definitions of variables and endpoints, internal consistency checks, and verification of missing or inconsistent values against the original clinical documentation. Missing data were handled by excluding patients with incomplete information relevant to the primary endpoint or key secondary endpoints. No formal sample size calculation was performed because of the retrospective observational design; all consecutive eligible patients treated between January 2023 and June 2025 were included.
Statistical analyses were planned to compare baseline characteristics, surgical management, treatment adequacy, diagnostic performance of frozen section analysis between study groups. Diagnostic performance of frozen section analysis was evaluated against definitive histopathology as the reference standard. Additional analyses were planned to account for potential confounding and to assess the robustness of the primary findings.
- Conditions
- Papillary Thyroid Cancer, Lymph Node Metastasis
- Being tested
- Frozen section analysis (FSA)
- Keywords
- Frozen section analysis, Papillary Thyroid Cancer, Central Neck Dissection, Clinically Node-Negative Thyroid Cancer, Intraoperative Decision-Making, Treatment Adequacy
- Medical subject headings
- Thyroid Cancer, Papillary, Lymphatic Metastasis
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Frozen section analysis (FSA)Procedure or surgery
Frozen section analysis (FSA) is an intraoperative pathological technique used to provide a rapid assessment of excised tissue during surgery. In this study, ipsilateral level VI lymph nodes were removed and immediately sent to the pathology department, where they were frozen, sectioned using standard cryostat techniques, stained with hematoxylin and eosin, and examined by an experienced pathologist. The result was reported intraoperatively as positive or negative for lymph node metastasis and used to support real-time surgical decision-making.
| Study group | Role | What they receive |
|---|---|---|
| FSA Group | Participants in the FSA group underwent hemithyroidectomy with selective ipsilateral central neck dissection. One or more ipsilateral level VI lymph nodes were removed during surgery and submitted for intraoperative frozen section analysis (FSA). The frozen section result was used to inform real-time surgical decision-making and to guide possible escalation or de-escalation of the surgical strategy. Receives: Procedure: Frozen section analysis (FSA) | |
| non-FSA Group | Participants in the non-FSA group underwent total thyroidectomy according to the 2015 American Thyroid Association guidelines and the institutional standard practice. The surgical strategy was based on preoperative cytology, cervical ultrasound findings, clinical risk assessment, and multidisciplinary evaluation. Central compartment lymph node management was performed according to the surgeon's judgment and preoperative findings. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Treatment adequacy
concordance between the surgical procedure performed and the minimum surgical treatment considered necessary for appropriate locoregional disease control, as determined retrospectively on the basis of final histopathological findings. Surgical treatment will be classified as adequate, overtreatment, or undertreatment. Overtreatment is defined as total thyroidectomy in patients ultimately found to have a solitary unilateral carcinoma without adverse pathological features. Undertreatment is defined as an insufficient surgical extent in the presence of adverse pathological features requiring a more comprehensive oncological procedure.
Measured: From surgery to availability of final histopathological report, approximately 2-4 weeks after surgery.
Secondary outcomes (2)
Complications
Complications will be assessed after thyroid surgery and classified as major or minor. Major complications include recurrent laryngeal nerve injury, hypoparathyroidism, and postoperative haemorrhage. Minor complications include seroma, haematoma, and wound infection.
Measured: From surgery to postoperative follow-up, approximately 30-60 days after surgery.
Length of hospital stay
Length of hospital stay will be measured as the number of days from the date of surgery to the date of hospital discharge.
Measured: From surgery to hospital discharge, usually within 1-3 days after surgery.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted22 Jun 2026
- Study start9 Jan 2023
- Primary completion27 Jun 2025
- Study completion19 Sep 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Papillary Thyroid CancerStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Retrospective
- Enrolment
- 66 participants (actual)
Sponsor and investigators
- Lead sponsor
- Eleonora Lori, MD
- Sponsor type
- University, hospital or other
- Collaborators
- University of Palermo
- Responsible party
- Sponsor-investigator, Eleonora Lori, MD, University of Roma La Sapienza
- Investigators
- Gregorio Scerrino, MD, Principal investigator, Policlinico "P. Giaccone" University of Palermo
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07659717
- Sponsor's protocol ID
- PA-1-RETRO-2026-TBD
- Status last verified
- Jun 2026
- First submitted
- 15 Jun 2026
- Last updated
- 24 Jun 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No: Individual participant data will not be made available to other researchers. The study is based on institutional clinical and pathological data collected during routine care, and data sharing is restricted by privacy regulations and institutional policies. Only aggregate and anonymized data supporting the results may be reported in the final manuscript and related publications.
Study at a glance
From the registry record, last updated by the sponsor on 24 Jun 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Frozen Section-Guided Selective Ipsilateral Central Neck Dissection in Bethesda V-VI Thyroid Nodules: A Pilot Cohort Study Informing Surgical Extent
- ClinicalTrials.gov ID
- NCT07659717
- Acronym / sponsor ID
- PA-1-RETRO-2026-TBD
- Conditions
- Papillary Thyroid Cancer, Lymph Node Metastasis
- Keywords
- Frozen section analysis, Papillary Thyroid Cancer, Central Neck Dissection, Clinically Node-Negative Thyroid Cancer, Intraoperative Decision-Making, Treatment Adequacy
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 66 participants (actual)
- Lead sponsor
- Eleonora Lori, MDUniversity, hospital or other
- Collaborators
- University of Palermo
- Study start
- 9 Jan 2023 (actual)
- Primary completion
- 27 Jun 2025 (actual)
- Study completion
- 19 Sep 2025 (actual)
- First posted
- 22 Jun 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The goal of this observational pilot cohort study is to evaluate the feasibility and clinical implications of frozen section analysis-guided selective ipsilateral central neck dissection in adult patients undergoing primary thyroid surgery for Bethesda V-VI thyroid nodules with a clinically node-negative neck.
The main questions it aims to answer are:
- Can intraoperative frozen section analysis of ipsilateral level VI lymph nodes meaningfully inform real-time surgical decision-making?
- Can this strategy support tailored escalation or de-escalation of central compartment surgery while minimizing unnecessary bilateral central neck dissection and its associated morbidity? Researchers will compare patients managed with ipsilateral central neck dissection and intraoperative frozen section analysis with patients managed without frozen section analysis, in order to evaluate differences in treatment adequacy, surgical decision-making, and pathological nodal assessment.
Participants will undergo primary thyroid surgery according to institutional practice. In patients managed with the frozen section analysis-guided strategy, one or more ipsilateral level VI lymph nodes will be removed during surgery and examined intraoperatively. The result of frozen section analysis may be used to guide the extent of central compartment surgery and the overall surgical strategy.
Detailed description
This observational retrospective cohort study was conducted in a tertiary referral endocrine surgery unit and was based on prospectively collected institutional data. The study included consecutive adult patients undergoing primary thyroid surgery for cytologically suspicious or malignant thyroid nodules, classified as Bethesda V or VI according to the Bethesda System for Reporting Thyroid Cytopathology.
The study was designed to evaluate whether an intraoperative strategy based on ipsilateral central neck dissection (ipsiCND) with frozen section analysis (FSA) could improve the adequacy of surgical treatment in selected patients with low-risk thyroid cancer, potentially reducing both overtreatment and undertreatment. The institutional protocol incorporating ipsiCND-FSA was introduced in September 2023. Patients treated before implementation of this protocol generally underwent total thyroidectomy according to the standard institutional practice in place at that time. After implementation of the protocol, hemithyroidectomy combined with ipsilateral central neck lymph node sampling and intraoperative frozen section analysis was systematically proposed as the preferred surgical strategy in appropriately selected patients. Total thyroidectomy remained an option for patients who declined the conservative approach after counselling regarding the malignant or suspicious nature of the thyroid nodule and the available surgical alternatives.
Eligible patients were adults aged 18 years or older with a solitary thyroid nodule measuring less than 2.5 cm in maximum diameter, classified as Bethesda V or VI on preoperative cytology, with a clinically node-negative neck documented by preoperative cervical ultrasound. Patients were considered only if they underwent primary thyroid surgery and had complete histopathological data available for the thyroid specimen and, when removed, central compartment lymph nodes. Patients with previous thyroid or neck surgery, known distant metastases at the time of surgery, incomplete clinical or pathological data relevant to the study endpoints, or reoperations such as completion thyroidectomy or secondary lymph node dissection were excluded.
All patients received detailed preoperative counselling and provided written informed consent before surgery. The information provided included the planned procedure, the possible need for intraoperative modification of the surgical strategy according to real-time findings and frozen section results, and the potential risks and benefits of the available surgical options. Patients also consented to the inclusion of their clinical and pathological data in the institutional database and to their use for research purposes. The study was conducted in accordance with the principles of the Declaration of Helsinki, followed good clinical practice standards, and was approved by the local Ethics Committee under protocol PA-1-RETRO-2026-TBD. Reporting was planned in accordance with the STROCCS recommendations for observational studies.
All surgical procedures were performed or supervised by experienced endocrine surgeons. Intraoperative nerve monitoring was routinely used in all cases as part of the standard institutional practice. The extent of thyroid surgery, either total thyroidectomy or lobectomy/isthmectomy, and the strategy for management of the central neck compartment were planned preoperatively according to cytological diagnosis, imaging findings, clinical risk profile, and institutional practice. In patients managed according to the ipsiCND-FSA protocol, the operative plan could be modified intraoperatively on the basis of frozen section findings.
Patients were stratified according to intraoperative management of the central compartment. In the FSA group, one or more ipsilateral level VI lymph nodes were removed during hemithyroidectomy and immediately submitted for frozen section analysis. Lymph nodes were processed using standard cryostat techniques, stained with hematoxylin and eosin, and evaluated intraoperatively by an experienced pathologist. The intraoperative nodal status was reported as positive or negative for metastatic disease. Definitive paraffin-embedded histopathology served as the reference standard for final assessment. In the non-FSA group, no intraoperative frozen section analysis of central compartment lymph nodes was performed. In this cohort, patients underwent total thyroidectomy, reflecting the inability to obtain sufficiently reliable preoperative risk stratification according to the standard approach used before implementation of the new protocol.
The primary objective of the study was to assess treatment adequacy. Treatment adequacy was defined as the concordance between the surgical procedure actually performed and the minimum surgical treatment considered necessary to achieve appropriate locoregional disease control on the basis of final histopathological findings. The minimum necessary extent of surgery was determined retrospectively, with particular attention to definitive tumor characteristics, including tumor focality and laterality, extrathyroidal extension, vascular invasion, aggressive histological variants, and nodal involvement.
Overtreatment was defined as performance of total thyroidectomy in patients who were ultimately found to have a solitary unilateral carcinoma without microscopic or macroscopic extrathyroidal extension, vascular invasion, or aggressive histological variants. Undertreatment was defined as an insufficient extent of surgery in the presence of adverse pathological features requiring a more comprehensive oncological procedure. These definitions were applied irrespective of study group allocation. For comparative analyses, overtreatment and undertreatment were also combined into a composite endpoint of surgical mis-treatment.
Secondary objectives included evaluation of the diagnostic performance of frozen section analysis for detecting central compartment lymph node metastases. Diagnostic performance was assessed by calculating sensitivity, specificity, positive predictive value, negative predictive value, overall accuracy, and the area under the receiver operating characteristic curve, using definitive histopathology as the reference standard. Additional secondary outcomes included postoperative complications and length of hospital stay. Postoperative complications included major complications such as recurrent laryngeal nerve injury, hypoparathyroidism, postoperative hemorrhage, and minor complications such as seroma, hematoma, and wound infection.
Clinical, surgical, pathological, and postoperative data were extracted from the prospectively maintained institutional database and cross-checked against source documents, including operative reports, pathology reports, ultrasound reports, discharge summaries, and postoperative follow-up records. Data quality was supported by predefined data fields, standardized definitions of variables and endpoints, internal consistency checks, and verification of missing or inconsistent values against the original clinical documentation. Missing data were handled by excluding patients with incomplete information relevant to the primary endpoint or key secondary endpoints. No formal sample size calculation was performed because of the retrospective observational design; all consecutive eligible patients treated between January 2023 and June 2025 were included.
Statistical analyses were planned to compare baseline characteristics, surgical management, treatment adequacy, diagnostic performance of frozen section analysis between study groups. Diagnostic performance of frozen section analysis was evaluated against definitive histopathology as the reference standard. Additional analyses were planned to account for potential confounding and to assess the robustness of the primary findings.
Study design
- Observational model
- Cohort
- Time perspective
- Retrospective
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| FSA Group | – | Procedure: Frozen section analysis (FSA)Participants in the FSA group underwent hemithyroidectomy with selective ipsilateral central neck dissection. One or more ipsilateral level VI lymph nodes were removed during surgery and submitted for intraoperative frozen section analysis (FSA). The frozen section result was used to inform real-time surgical decision-making and to guide possible escalation or de-escalation of the surgical strategy. |
| non-FSA Group | – | –Participants in the non-FSA group underwent total thyroidectomy according to the 2015 American Thyroid Association guidelines and the institutional standard practice. The surgical strategy was based on preoperative cytology, cervical ultrasound findings, clinical risk assessment, and multidisciplinary evaluation. Central compartment lymph node management was performed according to the surgeon's judgment and preoperative findings. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- The study population includes consecutive adult patients treated in a tertiary referral endocrine surgery unit who underwent primary thyroid surgery for cytologically suspicious or malignant thyroid nodules. Eligible patients had Bethesda V or VI thyroid cytology, a solitary low-risk thyroid nodule smaller than 2.5 cm, and a clinically node-negative neck documented by preoperative cervical ultrasound. All patients were managed according to institutional surgical protocols and had prospectively collected clinical, surgical, and histopathological data available for analysis.
Key inclusion criteria (10 listed)
- age 18 years or older.
- Adult patients undergoing primary thyroid surgery.
- Preoperative thyroid cytology classified as Bethesda V or Bethesda VI according to the Bethesda System for Reporting Thyroid Cytopathology.
- Presence of a solitary thyroid nodule.
- Maximum nodule diameter less than 2.5 cm.
Key exclusion criteria (5 listed)
- Age younger than 18 years.
- Previous thyroid or neck surgery, including completion thyroidectomy or secondary lymph node dissection
- Known cervical lymph node metastases or distant metastases at the time of surgery.
- Thyroid nodule measuring 2.5 cm or more in maximum diameter.
- Incomplete clinical and pathological data relevant to the study endpoints.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Frozen section analysis (FSA)Frozen section analysis (FSA) is an intraoperative pathological technique used to provide a rapid assessment of excised tissue during surgery. In this study, ipsilateral level VI lymph nodes were removed and immediately sent to the pathology department, where they were frozen, sectioned using standard cryostat techniques, stained with hematoxylin and eosin, and examined by an experienced pathologist. The result was reported intraoperatively as positive or negative for lymph node metastasis and used to support real-time surgical decision-making. | Procedure or surgery | FSA Group |
Primary outcome
Treatment adequacy
Time frame: From surgery to availability of final histopathological report, approximately 2-4 weeks after surgery.
concordance between the surgical procedure performed and the minimum surgical treatment considered necessary for appropriate locoregional disease control, as determined retrospectively on the basis of final histopathological findings. Surgical treatment will be classified as adequate, overtreatment, or undertreatment. Overtreatment is defined as total thyroidectomy in patients ultimately found to have a solitary unilateral carcinoma without adverse pathological features. Undertreatment is defined as an insufficient surgical extent in the presence of adverse pathological features requiring a more comprehensive oncological procedure.
2 secondary outcomes
Complications
Time frame: From surgery to postoperative follow-up, approximately 30-60 days after surgery.
Length of hospital stay
Time frame: From surgery to hospital discharge, usually within 1-3 days after surgery.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 24 Jun 2026.
- Individual participant dataSharing planned: No. Individual participant data will not be made available to other researchers. The study is based on institutional clinical and pathological data collected during routine care, and data sharing is restricted by privacy regulations and institutional policies. Only aggregate and anonymized data supporting the results may be reported in the final manuscript and related publications.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Gregorio Scerrino, MD principal investigator
Policlinico "P. Giaccone" University of Palermo
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Papillary Thyroid Cancer and Lymph Node Metastasis, run by Eleonora Lori, MD at 1 site in Italy.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 10 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 24 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Treatment adequacy (time frame: From surgery to availability of final histopathological report, approximately 2-4 weeks after surgery.). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Jun 2026.