Evaluation of the effect of levothyroxine in subclinical hypothyroidism
Phase 3
Recruiting
- Conditions
- Subclinical hypothyroidism.Sub clinical iodine-deficiency hypothyroidism
- Registration Number
- IRCT20200731048259N1
- Lead Sponsor
- Shahid Beheshti University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
People who have normal T4 and high TSH in their blood tests
Exclusion Criteria
Taking anti thyroid drugs and lithium
Treated with radiation therapy or thyroid surgery
Iodine deficiency
Pregnancy
Central disorder (pituitary gland)
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Percentage of people whose lipid profile is affected by levothyroxine treatment. Timepoint: At the beginning of the study And 7 days later and 3 and 6 months after taking levothyroxine. Method of measurement: Laboratory data.
- Secondary Outcome Measures
Name Time Method