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Papillary Thyroid CarcinomaNCT07391514

Deep Learning-Based Intraoperative Dual-tracer Video Analysis of Sentinel Lymph Node Mapping for Metastasis Prediction in cN0 Papillary Thyroid Carcinoma

An observational study of Papillary Thyroid Carcinoma, run by First Affiliated Hospital of Chongqing Medical University at 1 site in China.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The goal of this observational study is to learn if a computer program (deep learning) can accurately predict lymph node spread in adults with papillary thyroid cancer who have no signs of lymph node involvement before surgery (called cN0). Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Papillary Thyroid Carcinoma
What is being tested?
Indocyanine green (ICG) sentinel lymph node mapping, Carbon nanoparticle (CNs) sentinel lymph node mapping and Dual-tracer (ICG combined with CNs) sentinel lymph node mapping
Type of treatment
Injection or infusion
How many people
131 participants
Where
1 siteChina
Study dates
1 Apr 2024to 31 Oct 2024
How long will I take part?
12 Months
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: Adults diagnosed with clinically node-negative papillary thyroid carcinoma (cN0-PTC) who are scheduled to undergo surgical treatment at the Department of Breast and Thyroid Surgery, First Affiliated Hospital of Chongqing Medical University, Chongqing, China. Participants are identified through routine clinical care and preoperative evaluation. The study population includes patients with primary PTC confirmed by fine-needle aspiration biopsy who have no evidence of lymph node metastasis on preoperative ultrasound or other imaging studies. Both male and female adults aged 18 years and older are eligible regardless of tumor size, location, or genetic mutation status.

Who may be able to join

  • Age 18 years or older at the time of enrollment
  • Histologically confirmed papillary thyroid carcinoma (PTC) by preoperative fine-needle aspiration biopsy
  • Clinically node-negative (cN0) status confirmed by preoperative imaging (ultrasound and/or cross-sectional imaging showing no evidence of lymph node metastasis)
  • Scheduled to undergo thyroid surgery with simultaneous central lymph node dissection
  • Willing and able to provide written informed consent
  • Complete preoperative clinical data available, including:
Show all 11Show fewer
  • Demographic information (age, sex, body mass index)
  • Thyroid ultrasound report with detailed tumor characteristics
  • Fine-needle aspiration biopsy pathology report
  • Genetic testing results (when available)
  • Able to undergo intraoperative dual-tracer sentinel lymph node mapping with near-infrared fluorescence video recording

Who cannot join

  • History of previous neck surgery (including thyroid surgery, parathyroid surgery, or other cervical operations)
  • History of external beam radiotherapy to the head and neck region
  • Diagnosis of thyroid malignancy other than papillary thyroid carcinoma (e.g., follicular thyroid carcinoma, medullary thyroid carcinoma, anaplastic thyroid carcinoma, or thyroid lymphoma)
  • Known allergy or hypersensitivity to indocyanine green (ICG), iodine, or carbon nanoparticles
  • Severe hepatic insufficiency (ICG is metabolized by the liver)
  • Pregnancy or breastfeeding
Show all 11Show fewer
  • Incomplete medical records or missing essential preoperative data
  • Refusal to undergo dual-tracer imaging procedure
  • Inability to obtain satisfactory intraoperative near-infrared fluorescence video recording due to technical issues or poor image quality
  • Participation in another interventional clinical trial that may interfere with the current study
  • Any condition that, in the investigator's opinion, would compromise the participant's safety or the quality of the study data

Trial locations and contacts

1 site in 1 country.

China1 site
  • The First Affiliated Hospital of Chongqing Medical University

    Chongqing, 400016

Other trials in China

About this study

Official title: Deep Learning-Based Intraoperative Dual-tracer Video Analysis of Sentinel Lymph Node Mapping for Metastasis Prediction in cN0 Papillary Thyroid Carcinoma: A Prospective Cohort Study

The goal of this observational study is to learn if a computer program (deep learning) can accurately predict lymph node spread in adults with papillary thyroid cancer who have no signs of lymph node involvement before surgery (called cN0). The main questions it aims to answer are:

  • Can video analysis of lymph node mapping during surgery predict if cancer has spread to lymph nodes beyond the first-draining (sentinel) lymph node?
  • Can this prediction help surgeons decide how much tissue to remove during surgery?
Read more

During surgery, participants will receive an injection of two special dyes (carbon nanoparticles and indocyanine green) near the thyroid tumor. These dyes travel through the lymphatic system and help surgeons see the lymph nodes. A special camera records a video of how the dyes move and light up the lymph nodes.

Researchers will use computer programs to analyze these videos along with other medical information (such as ultrasound results and tumor characteristics) to predict whether cancer has spread to additional lymph nodes. The predictions will be compared against the actual results from tissue samples examined after surgery.

Participants will receive standard thyroid cancer surgery. The study does not change the surgical treatment. The video recording adds no extra risk to participants.

Read the detailed description

BACKGROUND AND RATIONALE:

Papillary thyroid carcinoma (PTC) is one of the fastest-growing cancers worldwide. A major challenge in treating PTC is that 30% to 80% of patients who appear to have no lymph node involvement before surgery (clinically node-negative, or cN0) actually have hidden (occult) cancer spread to their lymph nodes. Current imaging methods like ultrasound often miss these small areas of cancer spread.

This creates a difficult decision for surgeons: removing too many lymph nodes increases the risk of complications such as damage to the parathyroid glands (which control calcium levels) and the nerves that control the voice. However, removing too few lymph nodes may leave cancer behind, which can lead to recurrence.

Sentinel lymph node (SLN) mapping is a technique that identifies the first lymph nodes that drain from a tumor. The idea is that if cancer spreads through the lymphatic system, it will reach these sentinel nodes first. However, current single-tracer methods for SLN mapping in thyroid cancer have limitations and variable results.

This study uses a dual-tracer approach that combines two different dyes:

  1. Carbon nanoparticles (CNs): These provide long-lasting black staining that helps surgeons see lymph nodes clearly
  2. Indocyanine green (ICG): This dye glows under near-infrared light, allowing real-time visualization of lymphatic flow

By combining these two tracers, surgeons can see both the structure of lymph nodes and how lymphatic fluid flows through them over time.

STUDY DESIGN:

This is a prospective, single-center, observational cohort study. The study does not change the surgical treatment that participants receive. All participants undergo standard thyroid cancer surgery with lymph node removal as determined by their surgical team.

STUDY PROCEDURES:

  1. Pre-operative Assessment: All participants undergo standard pre-operative evaluation including:
  • Physical examination
  • Thyroid ultrasound with detailed lymph node assessment
  • Fine-needle aspiration biopsy to confirm PTC diagnosis
  • Genetic testing for common mutations (such as BRAF)
  • Standard blood tests
  1. Surgical Procedure: During surgery, participants receive the dual-tracer injection under ultrasound guidance. The injection is given at multiple points around the thyroid tumor. The specific preparation is:
  • 0.1 ml of ICG solution (concentration: 2.5 mg/ml)
  • 0.1 ml of carbon nanoparticle suspension (concentration: 50 mg/ml) These are mixed together and injected using precise, multi-point technique.
  1. Video Recording: A near-infrared fluorescence imaging system records the entire process of lymph node visualization. The recording captures:
  • How the dyes spread through the lymphatic channels
  • When each lymph node first becomes visible
  • How the fluorescence signal changes over time
  • The pattern of lymphatic drainage Videos are recorded at high resolution (1920 × 1080 pixels) at approximately 30 frames per second. A standardized 3-minute segment is extracted from each video for analysis, providing 150 frames per patient.
  1. Surgical Decisions: The sentinel lymph node (the first node that lights up) is removed and sent for immediate frozen section analysis. Based on standard criteria, surgeons decide whether to perform:
  • Ipsilateral central lymph node dissection (removing lymph nodes on the same side as the tumor)
  • Lateral lymph node dissection (if certain criteria are met)
  • Contralateral central dissection (removing lymph nodes on the opposite side) These decisions follow the standard surgical protocol at our institution and are not influenced by the deep learning predictions.
  1. Pathological Examination:

All removed lymph nodes are examined by pathologists to determine:

  • Whether the sentinel lymph node contains cancer (SLNM status)
  • Whether second-echelon lymph nodes contain cancer (SeLNM)
  • Whether non-sentinel lymph nodes contain cancer (NsLNM)
  • The number and location of all positive lymph nodes

DATA COLLECTION AND ANALYSIS:

Clinical Data (32 variables):

  • Demographics: age, sex, body mass index
  • Ultrasound features: tumor size, location, margins, calcification patterns, aspect ratio, TI-RADS classification
  • Pathological features: multifocality, extrathyroidal extension, capsular invasion
  • Genetic data: BRAF mutation status and other relevant mutations

Video Analysis:

Two experienced surgeons (each with more than 10 years of experience) manually identify and outline the regions of interest (the sentinel lymph nodes) in each video frame. This creates 19,650 mask images across all participants.

Feature Extraction:

The deep learning system extracts multiple types of features:

Spatial Features (2,048 dimensions):

  • Image features from a pre-trained neural network (EfficientNet-B5)
  • Grayscale characteristics
  • Shape and morphological features
  • Hu moment descriptors (mathematical descriptions of shape)

Temporal Features (20 dimensions):

  • Frame-to-frame differences showing how the image changes
  • Optical flow measurements showing movement patterns
  • Fluorescence intensity changes over time
  • Flow velocity measurements at specific time points

DEEP LEARNING MODELS:

Nine different deep learning architectures are developed and compared:

  1. Convolutional Neural Network (CNN): Extracts local spatial features from images
  2. Long Short-Term Memory (LSTM): Captures patterns in time-series data
  3. CNN + LSTM: Combines spatial and temporal feature extraction
  4. CNN + LSTM + Attention: Adds attention mechanism to focus on important time points
  5. Transformer: Uses self-attention to capture global patterns in sequential data
  6. Crossformer: A specialized architecture for time-series analysis
  7. 3D-CNN: Processes video data as three-dimensional volumes
  8. LSTM + Transformer: Hybrid model combining LSTM and Transformer strengths
  9. LSTM + Crossformer: Hybrid model combining LSTM and Crossformer

All models use:

  • Binary cross-entropy loss function
  • Adam optimizer for training
  • Data augmentation (rotation, scaling, noise injection) to prevent overfitting
  • Weighted loss functions to handle class imbalance
  • Dropout regularization

MODEL EVALUATION:

Models are evaluated using 10-fold stratified cross-validation, ensuring balanced distribution of outcomes in training and testing sets. Performance metrics include:

  • Area Under the ROC Curve (AUC): Measures overall discrimination ability
  • Accuracy: Percentage of correct predictions
  • Sensitivity: Ability to correctly identify patients with metastasis
  • Specificity: Ability to correctly identify patients without metastasis
  • Positive Predictive Value: Probability that a positive prediction is correct
  • Negative Predictive Value: Probability that a negative prediction is correct
  • F1 Score: Balance between precision and recall
  • Brier Score: Calibration of predicted probabilities

Additional analyses include:

  • Decision curve analysis to assess clinical utility
  • Calibration curves to check prediction reliability
  • Learning curves to assess overfitting
  • DeLong test for statistical comparison between models
  • Probability-based model ranking approach (PMRA)

MODEL INTERPRETABILITY:

To understand how the model makes predictions, we use SHapley Additive exPlanations (SHAP) analysis. This technique:

  • Identifies which features contribute most to predictions
  • Shows how each feature affects individual predictions
  • Reveals whether the model relies on clinically meaningful factors
  • Provides transparency into the "black box" of deep learning

OUTCOMES:

Primary Outcomes:

  1. Second-echelon lymph node metastasis (SeLNM): Cancer spread to lymph nodes beyond the sentinel node in the drainage pathway
  2. Non-sentinel lymph node metastasis (NsLNM): Cancer spread to any lymph node other than the sentinel node

Both outcomes are determined by final pathological examination of surgically removed tissue (the gold standard).

Secondary Outcomes:

  • Model performance metrics (AUC, sensitivity, specificity, etc.)
  • Feature importance rankings from SHAP analysis
  • Comparison of model architectures

STATISTICAL CONSIDERATIONS:

Sample Size:

Based on power calculations assuming:

  • Alpha = 0.05 (significance level)
  • Power = 0.80
  • Expected sensitivity difference of 20% between methods
  • Expected prevalence of lymph node metastasis of 50%

A minimum of 335 participants was calculated. Due to strict inclusion criteria and video quality requirements, 131 participants with complete, high-quality data were included in the final analysis.

Statistical Methods:

  • Descriptive statistics for baseline characteristics
  • Chi-square or Fisher exact test for categorical variables
  • Mann-Whitney U test for continuous variables
  • DeLong test for comparing AUC values between models
  • 95% confidence intervals for all performance metrics

FOLLOW-UP:

While the primary analysis focuses on intraoperative prediction, participants are followed according to standard clinical care protocols. Long-term outcomes including recurrence-free survival may be analyzed in future studies.

ETHICAL CONSIDERATIONS:

This study was approved by the Ethics Committee of the First Affiliated Hospital of Chongqing Medical University (Approval No. 2023-322). All participants provided written informed consent before enrollment.

The study poses minimal additional risk to participants because:

  • The dual-tracer injection uses agents already approved for clinical use
  • The video recording is non-invasive and does not affect surgical decisions
  • All surgical decisions are made according to standard protocols
  • The deep learning analysis is performed retrospectively and does not influence treatment

POTENTIAL IMPACT:

If successful, this approach could:

  1. Help surgeons make more informed decisions about the extent of lymph node removal
  2. Reduce unnecessary extensive surgery in low-risk patients
  3. Ensure adequate surgery in high-risk patients who might otherwise be undertreated
  4. Provide real-time, objective decision support during surgery
  5. Standardize the interpretation of lymphatic mapping across different surgeons and centers
  6. Serve as a training tool for less experienced surgeons

LIMITATIONS:

  • Single-center study, which may limit generalizability
  • Relatively small sample size due to strict quality requirements
  • Manual annotation of regions of interest may introduce variability
  • Deep learning models require validation in external cohorts
  • Real-time implementation during surgery requires further development

FUTURE DIRECTIONS:

  • External validation in multiple centers
  • Development of real-time prediction software for intraoperative use
  • Integration with other imaging modalities
  • Prospective interventional trials to assess clinical benefit of AI-guided surgery
Being tested
Indocyanine green (ICG) sentinel lymph node mapping, Carbon nanoparticle (CNs) sentinel lymph node mapping, Dual-tracer (ICG combined with CNs) sentinel lymph node mapping
Keywords
Papillary thyroid carcinoma, Sentinel lymph node biopsy, Dual-tracer imaging, Indocyanine green, Carbon nanoparticles, Deep learning
Medical subject headings
Thyroid Cancer, Papillary

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Indocyanine green (ICG) sentinel lymph node mappingDiagnostic test

    Also called ICG fluorescence lymphography, Near-infrared fluorescence sentinel lymph node identification

    Intraoperative sentinel lymph node mapping using indocyanine green (ICG) with near-infrared fluorescence imaging.

    Preparation: ICG powder (25 mg) is dissolved in 10 ml sterile water to achieve a concentration of 2.5 mg/ml.

    Administration: 0.2 ml of ICG solution is injected at multiple points around the thyroid tumor under real-time ultrasound guidance using a precision multi-point stereotactic injection technique.

    Visualization: A near-infrared fluorescence imaging system (excitation wavelength 750-800 nm, emission wavelength 820 nm) is used to visualize lymphatic channels and identify sentinel lymph nodes in real time during surgery.

    The sentinel lymph node is defined as the first lymph node that shows fluorescence signal after tracer injection.

  • Carbon nanoparticle (CNs) sentinel lymph node mappingDiagnostic test

    Also called Carbon nanoparticle suspension lymph node tracing, Nano-carbon lymphatic mapping

    Intraoperative sentinel lymph node mapping using carbon nanoparticle suspension with visual identification.

    Preparation: Carbon nanoparticle suspension is used at the commercial concentration of 50 mg/ml.

    Administration: 0.2 ml of carbon nanoparticle suspension is injected at multiple points around the thyroid tumor under real-time ultrasound guidance using a precision multi-point stereotactic injection technique.

    Visualization: Carbon nanoparticles (diameter 150 nm) selectively enter lymphatic channels and accumulate in lymph nodes, producing visible black staining. Surgeons identify sentinel lymph nodes by direct visual inspection of black-stained nodes.

    The sentinel lymph node is defined as the first lymph node that shows black staining after tracer injection.

  • Dual-tracer (ICG combined with CNs) sentinel lymph node mappingDiagnostic test

    Also called Combined ICG and carbon nanoparticle lymphatic mapping, Dual-tracer fluorescence and visual lymph node identification

    Intraoperative sentinel lymph node mapping using combined indocyanine green and carbon nanoparticles with near-infrared fluorescence imaging and visual identification.

    Preparation: 0.1 ml of ICG solution (2.5 mg/ml) is mixed with 0.1 ml of carbon nanoparticle suspension (50 mg/ml) to form a 0.2 ml dual-tracer composite agent.

    Administration: The mixed tracer is injected at multiple points around the thyroid tumor under real-time ultrasound guidance using a precision multi-point stereotactic injection technique.

    Visualization: Near-infrared fluorescence imaging captures real-time lymphatic flow dynamics (ICG component), while black staining provides durable visual lymph node identification (CNs component). Video recording documents the entire sentinel lymph node visualization process for at least 5 minutes at 1920x1080 resolution.

    Deep learning analysis: In this group, video recordings are analyzed using nine deep learning models to extract spatiotemporal features and predict second

Study groups in NCT07391514
Study groupRoleWhat they receive
ICG GroupAdults with clinically node-negative papillary thyroid carcinoma (cN0-PTC) who undergo intraoperative sentinel lymph node mapping using indocyanine green (ICG) alone. Intervention: 0.2 ml of ICG solution (concentration: 2.5 mg/ml) injected at multiple points around the thyroid tumor under ultrasound guidance. Near-infrared fluorescence imaging is used to visualize lymphatic drainage and identify sentinel lymph nodes. Participants undergo standard thyroid surgery including thyroid lobectomy and central lymph node dissection, with additional dissection based on intraoperative findings.
Receives: Diagnostic Test: Carbon nanoparticle (CNs) sentinel lymph node mapping
CNs GroupAdults with clinically node-negative papillary thyroid carcinoma (cN0-PTC) who undergo intraoperative sentinel lymph node mapping using carbon nanoparticles (CNs) alone. Intervention: 0.2 ml of carbon nanoparticle suspension (concentration: 50 mg/ml) injected at multiple points around the thyroid tumor under ultrasound guidance. Black staining is used to visualize lymph nodes during surgery. Participants undergo standard thyroid surgery including thyroid lobectomy and central lymph node dissection, with additional dissection based on intraoperative findings.
Receives: Diagnostic Test: Indocyanine green (ICG) sentinel lymph node mapping
ICG+CNs Group (Dual-Tracer)Adults with clinically node-negative papillary thyroid carcinoma (cN0-PTC) who undergo intraoperative sentinel lymph node mapping using combined indocyanine green and carbon nanoparticles (dual-tracer technique). Intervention: A mixture of 0.1 ml ICG solution (concentration: 2.5 mg/ml) and 0.1 ml carbon nanoparticle suspension (concentration: 50 mg/ml) injected at multiple points around the thyroid tumor under ultrasound guidance. Near-infrared fluorescence imaging combined with visual black staining is used to visualize lymphatic drainage and identify sentinel lymph nodes. This group also undergoes deep learning video analysis of the fluorescence imaging process to predict lymph node metastasis. Participants undergo standard thyroid surgery including thyroid lobectomy and central lymph node dissection, with additional dissection based on intraoperative findings.
Receives: Diagnostic Test: Dual-tracer (ICG combined with CNs) sentinel lymph node mapping

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Sentinel Lymph Node Metastasis (SLNM) Status

    The presence or absence of cancer metastasis in the sentinel lymph node, determined by postoperative histopathological examination (paraffin section) as the gold standard. SLNM is classified as positive (macrometastasis or micrometastasis present) or negative (no metastasis). The SLNM rate is calculated as: number of participants with positive sentinel lymph nodes divided by total number of participants with successfully identified sentinel lymph nodes.

    Measured: immediately after the surgery

  2. Sentinel Lymph Node Detection Rate

    The proportion of participants in whom sentinel lymph nodes are successfully identified using each tracer method (ICG alone, CNs alone, or ICG+CNs dual-tracer). A sentinel lymph node is defined as the first lymph node visualized after tracer injection. Detection rate is calculated as: number of participants with successfully identified sentinel lymph nodes divided by total number of participants in each group, expressed as a percentage.

    Measured: immediately after the surgery

  3. Second-Echelon Lymph Node Metastasis (SeLNM)

    The presence or absence of cancer metastasis in second-echelon lymph nodes (lymph nodes beyond the sentinel node in the lymphatic drainage pathway), determined by postoperative histopathological examination. SeLNM is the primary prediction target for the deep learning models in the ICG+CNs group. SeLNM status is classified as positive or negative based on paraffin section pathology results.

    Measured: perioperatively

  4. Non-Sentinel Lymph Node Metastasis (NsLNM)

    The presence or absence of cancer metastasis in any lymph node other than the sentinel lymph node, determined by postoperative histopathological examination. NsLNM includes metastasis in central compartment nodes (prelaryngeal, pretracheal, paratracheal, and nodes posterior to recurrent laryngeal nerve) and lateral compartment nodes when dissected. NsLNM is the second primary prediction target for the deep learning models in the ICG+CNs group.

    Measured: perioperatively

Secondary outcomes (6)
  1. Sensitivity of Sentinel Lymph Node Mapping

    The ability of each tracer method to correctly identify participants who have lymph node metastasis. Sensitivity is calculated as: true positives divided by (true positives + false negatives), expressed as a percentage. A true positive is defined as a positive sentinel lymph node in a participant with confirmed central lymph node metastasis on final pathology. Compared among ICG, CNs, and ICG+CNs groups.

    Measured: through study completion, an average of 1 year

  2. Specificity of Sentinel Lymph Node Mapping

    The ability of each tracer method to correctly identify participants who do not have lymph node metastasis. Specificity is calculated as: true negatives divided by (true negatives + false positives), expressed as a percentage. A true negative is defined as a negative sentinel lymph node in a participant with no central lymph node metastasis on final pathology. Compared among ICG, CNs, and ICG+CNs groups.

    Measured: through study completion, an average of 1 year

  3. Positive Predictive Value (PPV) of Sentinel Lymph Node Mapping

    The probability that participants with a positive sentinel lymph node truly have central lymph node metastasis. PPV is calculated as: true positives divided by (true positives + false positives), expressed as a percentage. Compared among ICG, CNs, and ICG+CNs groups.

    Measured: through study completion, an average of 1 year

  4. Negative Predictive Value (NPV) of Sentinel Lymph Node Mapping

    The probability that participants with a negative sentinel lymph node truly do not have central lymph node metastasis. NPV is calculated as: true negatives divided by (true negatives + false negatives), expressed as a percentage. A high NPV indicates that a negative sentinel lymph node reliably rules out metastatic disease. Compared among ICG, CNs, and ICG+CNs groups.

    Measured: through study completion, an average of 1 year

  5. Deep Learning Model Performance - Area Under ROC Curve (AUC)

    The area under the receiver operating characteristic curve for each deep learning model (CNN, LSTM, CNN+LSTM, CNN+LSTM+Attention, Transformer, Crossformer, 3D-CNN, LSTM+Transformer, LSTM+Crossformer) in predicting SeLNM and NsLNM in the ICG+CNs group. AUC ranges from 0 to 1, with higher values indicating better discrimination. Evaluated using 10-fold stratified cross-validation.

    Measured: through study completion, an average of 1 year

  6. Deep Learning Model Performance - Accuracy, Sensitivity, and Specificity

    Performance metrics of the optimal deep learning model for predicting SeLNM and NsLNM in the ICG+CNs group. Accuracy is the proportion of correct predictions. Sensitivity is the proportion of actual positive cases correctly identified. Specificity is the proportion of actual negative cases correctly identified. All metrics expressed as percentages with 95% confidence intervals.

    Measured: through study completion, an average of 1 year

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted6 Feb 2026
  2. Study start1 Apr 2024
  3. Primary completion31 Oct 2024
  4. Study completion31 Oct 2024

Resources

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
Prospective
Enrolment
131 participants (actual)
Target duration
12 Months
IDs, dates and publications
ClinicalTrials.gov ID
NCT07391514
Sponsor's protocol ID
1stChongqingMU-sxl
Status last verified
Feb 2026
First submitted
19 Jan 2026
Last updated
6 Feb 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided: A decision regarding individual participant data sharing has not yet been finalized. The study team is currently evaluating: 1. Technical feasibility of de-identifying video-based imaging data 2. Institutional and ethical requirements for data sharing 3. Development of appropriate data use agreements The IPD sharing plan will be updated prior to publication of the primary study results. Interested researchers may contact the Principal Investigator (suxinliang@21cn.com) to discuss potential future data access.

Publications

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    PubMed 39556263
  • Ding X, Liu Y, Zhao J, Wang R, Li C, Luo Q, Shen C. A novel wavelet-transform-based convolution classification network for cervical lymph node metastasis of papillary thyroid carcinoma in ultrasound images. Comput Med Imaging Graph. 2023 Oct;109:102298. doi: 10.1016/j.compmedimag.2023.102298. Epub 2023 Sep 9.

    PubMed 37769402
  • Yang D, Li T, Li L, Chen S, Li X. Multi-modal convolutional neural network-based thyroid cytology classification and diagnosis. Hum Pathol. 2025 Jul;161:105868. doi: 10.1016/j.humpath.2025.105868. Epub 2025 Jul 4.

    PubMed 40617519
  • Chu X, Wang T, Chen M, Li J, Wang L, Wang C, Wang H, Wong ST, Chen Y, Li H. Deep learning model for malignancy prediction of TI-RADS 4 thyroid nodules with high-risk characteristics using multimodal ultrasound: A multicentre study. Comput Med Imaging Graph. 2025 Sep;124:102576. doi: 10.1016/j.compmedimag.2025.102576. Epub 2025 May 26.

    PubMed 40446583
  • Liang M, Zhu T, Huang N, Zhang L, Yang C, Gao H, Zhang X, Li P, Cheng M, Wang K. Incorporating sentinel chain involvement pattern to predict non-sentinel lymph nodes status in breast cancer after neoadjuvant chemotherapy. Clin Transl Oncol. 2026 Jan;28(1):203-214. doi: 10.1007/s12094-025-03993-z. Epub 2025 Jul 31.

    PubMed 40745244
  • Mittendorf EA, Hunt KK, Boughey JC, Bassett R, Degnim AC, Harrell R, Yi M, Meric-Bernstam F, Ross MI, Babiera GV, Kuerer HM, Hwang RF. Incorporation of sentinel lymph node metastasis size into a nomogram predicting nonsentinel lymph node involvement in breast cancer patients with a positive sentinel lymph node. Ann Surg. 2012 Jan;255(1):109-15. doi: 10.1097/SLA.0b013e318238f461.

    PubMed 22167004
  • Zhou L, Yao J, Ou D, Li M, Lei Z, Wang L, Xu D. A multi-institutional study of association of sonographic characteristics with cervical lymph node metastasis in unifocal papillary thyroid carcinoma. Front Endocrinol (Lausanne). 2022 Sep 23;13:965241. doi: 10.3389/fendo.2022.965241. eCollection 2022.

    PubMed 36213266
  • Khan SU, Fatima K, Malik F, Kalkavan H, Wani A. Cancer metastasis: Molecular mechanisms and clinical perspectives. Pharmacol Ther. 2023 Oct;250:108522. doi: 10.1016/j.pharmthera.2023.108522. Epub 2023 Sep 1.

    PubMed 37661054
  • Cao R, Ji H, Feng N, Zhang Y, Yang X, Andersson P, Sun Y, Tritsaris K, Hansen AJ, Dissing S, Cao Y. Collaborative interplay between FGF-2 and VEGF-C promotes lymphangiogenesis and metastasis. Proc Natl Acad Sci U S A. 2012 Sep 25;109(39):15894-9. doi: 10.1073/pnas.1208324109. Epub 2012 Sep 11.

    PubMed 22967508
  • Li Y, Chen H, Zhao Y, Yan Q, Chen L, Song Q. circUBE2G1 interacts with hnRNPU to promote VEGF-C-mediated lymph node metastasis of lung adenocarcinoma. Front Oncol. 2024 Nov 27;14:1455909. doi: 10.3389/fonc.2024.1455909. eCollection 2024.

    PubMed 39664183
  • Guang Y, Wan F, He W, Zhang W, Gan C, Dong P, Zhang H, Zhang Y. A model for predicting lymph node metastasis of thyroid carcinoma: a multimodality convolutional neural network study. Quant Imaging Med Surg. 2023 Dec 1;13(12):8370-8382. doi: 10.21037/qims-23-318. Epub 2023 Nov 7.

    PubMed 38106318
  • Luo QW, Gao S, Lv X, Li SJ, Wang BF, Han QQ, Wang YP, Guan QL, Gong T. A novel tool for predicting the risk of central lymph node metastasis in patients with papillary thyroid microcarcinoma: a retrospective cohort study. BMC Cancer. 2022 Jun 2;22(1):606. doi: 10.1186/s12885-022-09655-5.

    PubMed 35655253
  • Popadich A, Levin O, Lee JC, Smooke-Praw S, Ro K, Fazel M, Arora A, Tolley NS, Palazzo F, Learoyd DL, Sidhu S, Delbridge L, Sywak M, Yeh MW. A multicenter cohort study of total thyroidectomy and routine central lymph node dissection for cN0 papillary thyroid cancer. Surgery. 2011 Dec;150(6):1048-57. doi: 10.1016/j.surg.2011.09.003.

    PubMed 22136820
  • Huang C, Cong S, Shang S, Wang M, Zheng H, Wu S, An X, Liang Z, Zhang B. Web-Based Ultrasonic Nomogram Predicts Preoperative Central Lymph Node Metastasis of cN0 Papillary Thyroid Microcarcinoma. Front Endocrinol (Lausanne). 2021 Sep 7;12:734900. doi: 10.3389/fendo.2021.734900. eCollection 2021.

    PubMed 34557165
  • Wang Y, Deng C, Shu X, Yu P, Wang H, Su X, Tan J. Risk Factors and a Prediction Model of Lateral Lymph Node Metastasis in CN0 Papillary Thyroid Carcinoma Patients With 1-2 Central Lymph Node Metastases. Front Endocrinol (Lausanne). 2021 Oct 15;12:716728. doi: 10.3389/fendo.2021.716728. eCollection 2021.

    PubMed 34721289

Questions about this trial

What is this clinical trial studying?

An observational study of Papillary Thyroid Carcinoma, run by First Affiliated Hospital of Chongqing Medical University at 1 site in China.

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 11 inclusion and 11 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 6 Feb 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 China. 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?

Sentinel Lymph Node Metastasis (SLNM) Status (time frame: immediately after the surgery). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07391514, which also lists 46 linked publications.

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 6 Feb 2026.

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