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Completed

NCT Number: NCT05025046

NGS-based Thyroscan Genomic Classifier in the Diagnosis of Thyroid Nodules

The purpose of this study is to evaluate the accuracy of Thyroscan in the differential diagnosis of benign and malignant thyroid nodules with suspecious ultrasound features

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

The First Peple's Hospital of Changzhou, Changzhou, Jiangsu, China

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About this study

The prevalence of thyroid nodules by high-resolution ultrasound can be as high as 20%, though most of them are benign lesions, only about 5%-15% are malignant lesions. Based on 1.4 billion population in China, there are approximately 280 million thyroid nodule carriers, of which approximately 14-42 million are potential patients with thyroid cancer. Now thyroid cancer is the fastest growing cancer and the 4th most common cancer in women in China. Therefore, the key point in the evaluation of thyroid nodules is the differential diagnosis of benign and malignant nodules. At present, the commonly used imaging and cytological diagnostic techniques for thyroid nodules include ultrasound and ultrasound-guided fine needle aspiration biopsy (FNAB), as well as emerging molecular diagnostic techniques.

The purpose of this study is to evaluate the accuracy of Thyroscan in the diagnosis of benign and malignant thyroid nodules with suspecious ultrasound features. For patients who have signed an informed consent, the subjects undergo fine needle aspiration of thyroid nodules classified as C-TIRADS catagories 3 or 4 under the guidance of ultrasound or palpation before receiving surgical treatment. One needle is used to prepare cytological smear, and one needle is preserved and sent to Thyroscan detection.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients sign the informed consent form for participating in the reasearch study.
  • Patient's age is 18 years or older.
  • Ultrasound showed at least one thyroid nodule, and it was classified as C-TIRADS Category 3/4.
  • The surgeon has confirmed surgical indication and the subject is willing to undergo the planned surgical intervention at the participating medical institution; or cytology results are benign, and the nodule(s) have remained clinically stable-defined as absence of new high-risk ultrasound features and no significant change in size on serial imaging.
  • Surgical indications include but are not limited to one of the following conditions: 1) Thyroid nodules are compressed or affect aesthetics; 2) The patient's subjective wishes require surgical removal of the nodules; 3) FNA samples with indeterminate cytology are classified as Bethesda III and IV, requiring diagnostic surgery; 4) After the investigator's assessment, there are other surgical indications.
  • Preoperative FNAB to obtain sufficient cells.

Exclusion criteria

  • The subject has a history of thyroid tumor.
  • The subject is not suitable for fine-needle aspiration biopsy and surgical treatment due to other conditions such as comorbid diseases.
  • Subjects who intend to receive the radiofrequency ablation therapy.
  • Other conditions determined by the researcher that do not meet the criteria of enrollment.

Treatment and study plan

Thyroscan

Diagnostic Test

To evaluate the accuracy of Thyroscan in the differential diagnosis of benign and malignant thyroid nudules with abnormal ultrasound features.

Primary outcomes

  1. To evaluation of Thyroscan's performance in diagnosing thyroid nodules

    Time frame: At the time of postsurgical pathology report, or upon completion of the 12-month follow-up for non-surgical participants.

    To explore the sensitivity, specificity, positive predictive value, negative predictive value, consistency and Kappa value of Thyroscan in the diagnosis of thyroid nodules with ultrasound features classified as C-TIRADS category 3/4.

Secondary outcomes

  1. To compared with cytopathology and Thyroscan in diagnosing thyroid nodules.

    Time frame: At the time of postsurgical pathology report, or upon completion of the 12-month follow-up for non-surgical participants.

Other outcomes

  1. To reveals the correlation between molecular landscape and clinical-pathological characteristics of thyroid nodules.

    Time frame: At the time of postsurgical pathology report, or upon completion of the 12-month follow-up for non-surgical participants.

Sponsors and collaborators

Lead sponsor

Rigen Biotech

Industry

Collaborators

  • RenJi Hospital
  • The First People's Hospital of Changzhou
  • Tianjin Medical University Cancer Institute and Hospital
  • Zhejiang Provincial People's Hospital

Registry information

Official study title

Prospective, Blinded, Multi-center Clincal Study of NGS-based Thyroscan Genomic Classifier in the Diagnosis of Thyroid Nodules

Important dates

Study start
2021
Primary completion
2024
Study completion
2024
First posted
Aug 27, 2021
Registry last updated
Aug 14, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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