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Molecular basis and Clinical study of thyroid tumor

Molecular basis and Clinical study of thyroid tumor

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300070912
Enrollment
Unknown
Registered
2023-04-26
Start date
2020-08-01
Completion date
Unknown
Last updated
2023-06-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Thyroid cancer

Interventions

Gold Standard:Needle capillary biopsy or pathological results after surgery
Index test:Eight novel thyroid hormone metabolites were tested in this study, including: iodothyronine, 3-iodothyronine, 3' -iodothyronine, 3-iodothyronine, 3, 5-diiodothyronine, 3', 5' -diiodothyroni

Sponsors

Xuzhou Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1) Thyroid cancer group: differentiated thyroid cancer patients aged 25-75 years with clinical surgical pathology; 2) Benign thyroid nodule group: patients with benign thyroid nodule aged 25-75 years with puncture cytology or clinical surgical pathology; 3) Healthy volunteers group: healthy volunteers aged 25-75 years with clinical ultrasound reports without thyroid nodule.

Exclusion criteria

Exclusion criteria: The individuals in DTC group are the patients with thyroid cancer diagnosed by biopsy. The serum samples were collected before surgery. The individuals will be excluded if they have the following conditions: (1) Abnormal thyroid function (Hyperthyroidism, hypothyroidism etc.); (2) Having a history of chemoradiotherapy; (3) Having other site tumors; (4) Having a history of surgery or blood transfusion in the past six months; (5) Having severe liver or kidney diseases; (6) Having metabolic diseases (Diabetes, Hyperlipidemia etc.); (6) Having immune system diseases (Lupus erythematosus, HIV etc.) The individuals in thyroid benign nodule group are the patients diagnosed by biopsy after FNA or surgery. The serum samples were collected before surgery or at the physical examination. The exclusion criteria were the same for patients in thyroid cancer group. The individuals in health control group are the volunteers without any thyroid tumor in ultrasonic detection. Additionally, the thyroid function and blood biochemical indexes of these volunteers were all in the normal range. The healthy female volunteers were also excluded from breast nodules and uterine fibroids.

Design outcomes

Primary

MeasureTime frame
diiodo-thyroxines;monoiodo-thyroxine;thyronine ;thyronamine;Sensitivity, SE;Specificity, SP;Positive predicative value, PPV;

Secondary

MeasureTime frame
Thyroxine ;triiodo-thyroxine;

Countries

China

Contacts

Public ContactLiang Jun

Xuzhou Central Hospital

mwlj521@163.com+86 18952171209

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026