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A Trial for the Evaluation of the Treatment and Outcome of Hyperthyroidism With Iodized Salt and Non Iodized Salt

A

Air Force Military Medical University of People's Liberation Army

Status

Unknown

Conditions

Hyperthyroidism

Treatments

Dietary Supplement: Iodine free diet group
Dietary Supplement: Normal iodine diet group

Study type

Interventional

Funder types

Other

Identifiers

NCT03444246
KY20172032-1

Details and patient eligibility

About

To clarify the influence of iodine intake in salt on the incidence and treatment of hyperthyroidism patients, so as to provide theoretical basis for accurate formulation of iodine intake in salt, and provide strategies for effective prevention and control of hyperthyroidism.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. sign informed consent before any research procedure is carried out
  2. men or women aged 18-65 (equal) at the age of 1.
  3. had been diagnosed as Graves hyperthyroidism
  4. patients with hyperthyroidism who had not been treated with drugs or stopped taking medicine for more than 3 months
  5. reduction to the current dose of hyperthyroidism for more than 2 months

Exclusion criteria

  1. during the period of pregnancy and lactation, those who plan to be pregnant during the study are not granted medical permission.

    Effective contraceptives

  2. for the last 1 months or the need for long-term use of amiodarone

  3. the history of anaphylaxis (such as systemic anaphylaxis, vasoedema, epidermal exfoliation) Etc.)

  4. consecutive use of beta receptor blockers for the last 2 weeks

  5. over the past six months, systemic use of corticosteroids (oral or intravenous) is continuous More than 7 days

  6. there was an obvious liver disease, showing one of the following cases: two consecutive weeks before A. visits.

It was confirmed that the measurements of AST or ALT were more than 3 times higher than the highest normal value (local data).

B. bilirubin synthesis and / or excretion disorders (such as hyperbilirubinemia), and other Decompensated liver diseases such as coagulation disorders, hepatic encephalopathy, hypoproteinemia, ascites, and esophagus Bleeding from varicose veins. C. acute viral, active, alcoholic, and alcoholic Other types of hepatitis 7 visits for 4 weeks before the 1 (or the local data), leukopenia (less than 3 * 10 9 /L) B/ 0 edition of the First Affiliated Hospital of The Fourth Military Medical University The First Affiliated Hospital, the Fourth Military Medical University B/0 Edition Seventh pages / 13 Pages Or neutropenia (less than 1.5 * 10 9 /L) 8 congestive heart failure at grade III or IV of the New York Heart Association (NYHA) 9 the past 3 months of visit to 1 had a major cardiovascular history, defined as: myocardial infarction Plug and coronary angioplasty or bypass surgery, valvular disease or repair, instability Angina pectoris, transient ischemic attack, or cerebrovascular accident 10 non well controlled atrial fibrillation 11 diagnosis of malignant tumors over the past 5 years 12 history of medullary thyroid carcinoma 13 organ transplantation or AIDS history 14 severe exophthalmos has influenced visual acuity 15 over the last 12 months, there is a history of alcohol abuse or drug abuse

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

60 participants in 2 patient groups

Iodine free diet group
Experimental group
Description:
The arm with non iodized salt,the subject in the non iodized salt group used the iodized salt for the first three months, and the iodized salt was changed after three months.
Treatment:
Dietary Supplement: Normal iodine diet group
Dietary Supplement: Iodine free diet group
Normal iodine diet group
Active Comparator group
Description:
The arm with iodized salt,the subject in the control group were consumed with iodized salt within six months.
Treatment:
Dietary Supplement: Normal iodine diet group

Trial contacts and locations

1

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Central trial contact

Qiuhe Ph.D Ji, Ph.D.,M.D.; Jie Ph.D Zhou, M.D.

Data sourced from clinicaltrials.gov

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