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Research on Excessive Iodine Status in Pregnancy

Chinese Academy of Medical Sciences & Peking Union Medical College logo

Chinese Academy of Medical Sciences & Peking Union Medical College

Status

Completed

Conditions

Neonatal Disorder
Pregnancy Related
Thyroid Dysfunction, Antepartum
Excessive Iodine Status

Treatments

Other: Dietary iodine intake restriction

Study type

Observational

Funder types

Other

Identifiers

NCT03422406
Liuyanping

Details and patient eligibility

About

To explore main cause and health impact of iodine excess during pregnancy, we performed iodine evaluation for 390 consecutive pregnant women from January 1st, 2016 to December 31st, 2016. Among them, 18 women (4.62%) with apparently elevated urinary iodine concentration (UIC) were enrolled onto this study for subsequent follow-up. History of high iodine exposure was collected from all participants. Parameters about iodine status were monitors until termination of pregnancy, and dietary iodine intake condition and thyroid function were also evaluated.

Full description

A prospective follow-up was arranged for the 18 pregnant women with excessive iodine status. History of iodine exposure (including hysterosalpingography (HSG) using an oil-soluble iodinated contrast medium, examination by computed tomography scan with contrast, administration of amiodarone, history of receiving radioiodine therapy, etc.) was collected from all participants. Evaluation of dietary iodine intake was performed through a 72-hour dietary recall.The serum iodine concentration (SIC) and urinary iodine concentration (UIC) were monitored continuously in the whole course of pregnancy. All subjects with excessive iodine load were recommended by nutritionists to have their dietary iodine intake restricted, and resume iodine-containing supplements and foods until the UIC<250 μg/L and SIC≤90 μg/L. After delivery, maternal colostrum iodine concentration and neonatal iodine status (including neonatal UIC, condition of congenital hypothyroidism screening tests, and thyroid physical examination) were also assessed.

Enrollment

18 patients

Sex

Female

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Pregnant women with apparently elevated urinary iodine concentration (UIC ≥250μg/L) and serum iodine concentration (SIC>90μg/L) were enrolled in this study.

Exclusion criteria

  • Subject who did not sign the informed consent or whose clinical date was not intact was excluded in our study.

Trial design

18 participants in 2 patient groups

HH group
Description:
Group (participants) with pre-gestational history of undergoing hysterosalpingography (HSG) using an oil-soluble iodinated contrast medium
Treatment:
Other: Dietary iodine intake restriction
Non-HH group
Description:
Group (participants) without pre-gestational history of undergoing hysterosalpingography (HSG)
Treatment:
Other: Dietary iodine intake restriction

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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