Graves’ disease,GD
Conditions
Interventions
Experimental group:Oral levothyroxine sodium tablets were supplemented with thyroid hormones. Vitamin D (5000 IU QOD) was also supplemented
Control group:Oral levothyroxine sodium tablets for thyroid hormone supplementation
Sponsors
Panzhihua Central Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. 131I treatment for GD patients. 2. After taking 131I for 1-3 months, TSH increases and/or FT4 decreases, indicating successful treatment of hyperthyroidism. 3. TRAb is higher than the reference value.
Exclusion criteria
Exclusion criteria: 1. Patients who have recently taken vitamin D (6 months prior to the study) 2. Active exophthalmos patients
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Thyrotropin Receptor Antibodies;25 hydroxyvitamin D;Thyroid hormone; | — |
Secondary
| Measure | Time frame |
|---|---|
| Blood calcium; | — |
Countries
China
Contacts
Public ContactWu Jie
Panzhihua Central Hospital
Outcome results
None listed