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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04396158
Other study ID # ovarian reserve
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date June 15, 2020
Est. completion date December 15, 2021

Study information

Verified date May 2020
Source Assiut University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Thyroid carcinoma is the most common endocrine malignancy. Surgery is the standard therapeutic approach for patients with differentiated thyroid carcinoma (DTC), followed by radioiodine (RAI) therapy if indicated. For women with DTC, the effects of RAI therapy on gonadal and reproductive function are an important consideration. This study aimed to evaluate the effects of RAI therapy on ovarian function.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 38
Est. completion date December 15, 2021
Est. primary completion date June 15, 2021
Accepts healthy volunteers No
Gender Female
Age group 15 Years to 45 Years
Eligibility Inclusion Criteria:

- Female patient in childbearing period.

- Female patient with differentiated thyroid carcinoma.

- Underwent thyroidectomy.

- Candidate for radioactive iodine therapy.

Exclusion Criteria:

- • Male patients.

- Postmenopausal female patients.

- Female patients with undifferentiated thyroid carcinoma.

- Pregnant female patients.

- Lactating female patients.

Study Design


Intervention

Radiation:
radioactive iodine
80-200 mCi of radioactive iodine will be given to thyroid cancer patients

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Assiut University

Outcome

Type Measure Description Time frame Safety issue
Primary Level of anti-Müllerian (AMH) hormone Level of anti-Müllerian (AMH) hormone in female patients before and after radioactive iodine therapy. 6 months
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