Iodine Status and Characteristics of Papillary Thyroid Cancer

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-65
SponsorShandong Provincial Hospital

About this trial

The effect of iodine on papillary thyroid cancer has been controversial for many years. The investigators designed a cross-sectional study and aimed to explore the relationship between the serum and urine iodine levels and the clinical and molecular characteristics of papillary thyroid cancer.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age range: 18~65 years old, gender not limited;

Living in the residential area for at least 5 years;

Patients diagnosed clinically with thyroid cancer and scheduled for thyroid surgery, with pathological diagnosis of papillary thyroid cancer;

Complete clinical data: including general information, relevant laboratory tests, pathological reports, surgical reports, ultrasound reports, etc.

Disqualifiers

Pathological diagnosis of other types of thyroid cancer;

Diagnosed with other types of cancer;

There are serious comorbidities of the heart, liver, and kidneys;

Trial population

Three sub centers will be selected in high iodine areas (Jining, Liaocheng, Heze) and moderate iodine areas (Jinan, Shenyang, Harbin) respectively. People who have lived in these areas for more than 5 years and seek medical treatment in tertiary hospitals will be selected.

Trial design

Design model

Case-only

Time perspective

Cross-sectional

Treatments tested in this trial

  • Iodine excess

    Dietary supplement

    Iodine excess areas: water iodine ≥100μg/L; or urinary iodine concentration(median urinary iodine levels in children aged 8-10 years old) ≥300μg/L

  • Iodine suitable

    Dietary supplement

    Iodine suitable areas: water iodine ≥40μg/L and ≤100μg/L; or urinary iodine concentration(median urinary iodine levels in children aged 8-10 years old) 100-199μg/L.

Treatment groups

600 Participants
are divided into 2 treatment groups
Group A: Excessive iodine group1 intervention
Group B: Suitable iodine group1 intervention

Trial outcomes

Primary outcomes

1

Serum and urine iodine levels

Time frame
1 year from enrollment
2

TNM staging of papillary thyroid cancer

Time frame
3 month from enrollment

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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