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Impact of Thyroid Treatment on Ovarian Function and Pregnancy Outcomes in Women with Differentiated Thyroid Cancer

Z

Zhejiang Provincial People's Hospital

Status

Not yet enrolling

Conditions

Thyroid Gland

Treatments

Procedure: Thyroid one-sided lobe + isthmus resection
Procedure: Total thyroidectomy + RAIT
Procedure: Total thyroidectomy

Study type

Interventional

Funder types

Other

Identifiers

NCT06845098
KY2024117-Ge

Details and patient eligibility

About

This project aims to study the effects of different types of thyroid surgery and RAIT on ovarian function and pregnancy outcomes of DTC women of childbearing age, analyze possible risk factors, and assess whether potential risk factors such as age, thyroid stimulating hormone (TSH) levels and positive thyroid antibodies are related to ovarian hypofunction and adverse pregnancy outcomes.

Full description

  1. Screen the patients in the group according to the inclusion and exclusion criteria and sign the informed consent form (a total of 300 patients were included). Fill in the questionnaire after joining the group. 2) Physical examination of patients before treatment (measure height, weight, waist circumference, hip circumference, body fat distribution and percentage); thyroid function test (thyroid B-ultrasound, TSH, FT3, FT4, TPO-Ab, TG-Ab); baseline ovarian function test (AMH, menstruation 1-3 days Six hormones, observe the ovarian condition and the number of sinus follicles through vaginal B-ultrasound); leave blood for scientific research: 2 tubes of coagulation (serum), 1 tube of whole blood, -80℃ freeze. 3) Different types of thyroid surgery (thyroid unilateral lobe + isthmus resection, total thyroidectomy, total thyroidectomy + RAIT) are treated. 4) 3, 6, 12 and 24 months after treatment, the patients in the group should be followed up on ovarian and thyroid function, including physical examination (measurement of height, weight, waist circumference, hip circumference, body fat distribution and percentage); thyroid function testing (thyroid B-ultrasound, TSH, FT3, FT4, TPO-Ab, T G-Ab); ovarian function test (AMH, six items of sex hormones for 1-3 days of menstruation, observation of ovarian conditions and the number of sinus follicles through vaginal B-ultrasound); retention of blood for scientific research: 2 tubes (serum) of blood-promoting blood, 1 tube of whole blood, -80℃ freezing; record adverse reactions and combined medication. 5) If the patient in the group is pregnant during the follow-up period, the pregnancy follow-up shall be carried out according to the CRF table items at 2, 4, 12, 28 and 37 weeks of pregnancy respectively; delivery follow-up shall be carried out on the day of delivery and 6 weeks after delivery. 6) After the research, collect and sort out data for statistical analysis, summarize and sort out the results and publish them in professional journals in relevant fields in the form of papers.

Enrollment

300 estimated patients

Sex

Female

Ages

20 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age 20-45 years old;
  2. Premenopausal women whose thyroid B-ultrasound + surgical pathology is clearly differentiated thyroid cancer (papillar thyroid cancer or follicular thyroid cancer);
  3. TNM stage is in stage I (T1-3, N0 or N1, M0);
  4. Treatment of thyroid tumor resection: unilateral lobe of the thyroid + isthmus resection, total thyroidectomy, total thyroidectomy + RAIT.

Exclusion criteria

  1. Patients with malignant tumors in other parts or low undifferentiated thyroid cancer;
  2. Patients with abnormal liver and kidney function;
  3. TNM stage II and above;
  4. History of ovarian surgery, hysterectomy, pelvic surgery or radiation therapy;
  5. Pregnancy;
  6. Have the following uterine abnormalities, such as uterine malformation (single-horned uterus, double uterus); untreated mediastinal uterus, submucosal uterine fibroids, multiple endometrial polyps, or severe uterine adhesion.
  7. Patients diagnosed with polycystic ovary syndrome by the Rotterdam standard;
  8. Patients with ovarian failure;
  9. Patients have infectious factors, immune diseases and metabolic diseases that may affect pregnancy outcomes;
  10. Pregnancy contraindications or diseases that have a clear impact on pregnancy.

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

300 participants in 3 patient groups

Thyroid one-sided lobe + isthmus resection
Experimental group
Description:
Thyroid one-sided lobe + isthmus resection
Treatment:
Procedure: Thyroid one-sided lobe + isthmus resection
Total thyroidectomy
Experimental group
Description:
Total thyroidectomy
Treatment:
Procedure: Total thyroidectomy
Total thyroidectomy + RAIT
Experimental group
Description:
Total thyroidectomy + RAIT
Treatment:
Procedure: Total thyroidectomy + RAIT

Trial contacts and locations

1

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Central trial contact

Minghua Ge

Data sourced from clinicaltrials.gov

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