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Clinical Trials/NCT04421053
NCT04421053
Unknown
Not Applicable

Gestational Weight Gain (GWG) Recommendations for Chinese Women With Gestational Diabetes Mellitus (GDM)

Peking Union Medical College Hospital1 site in 1 country4,050 target enrollmentMarch 24, 2020

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Gestational Diabetes
Sponsor
Peking Union Medical College Hospital
Enrollment
4050
Locations
1
Primary Endpoint
The incidence rate of infant outcomes
Last Updated
4 years ago

Overview

Brief Summary

The 2009 IOM recommendation value for weight gain during pregnancy is widely used. Due to the unclear relationship between gestational diabetes mellitus and weight gain during pregnancy when formulating this recommendation value, pregnant women with gestational diabetes mellitus were excluded from the study population. Control of appropriate weight gain and control of blood glucose stability is an important part of GDM management in pregnant women. The incidence of GDM in China is about 15%-20%, and the number of pregnant women with GDM ranks first in the world. For the sake of the current and long-term health of maternal and infant, it is of great significance to explore the appropriate weight gain range and formulate the recommended value for GDM pregnant women as an independent population. This project intends to use prospective cohort study of combining the observation of pregnant women with gestational diabetes blood sugar and weight changes, through the comparison of normal pregnant women suitable scope of weight gain, analyzes its influence on adverse pregnancy outcomes, increased the weight of gestational diabetes women recommended value is put forward, and combined with the Delphi expert consultation method for evaluation.

Detailed Description

This project is a prospective cohort study designed to investigated the changes in blood glucose and body weight in women with gestational diabetes during pregnancy. The study aimed to enroll 4000 participants, using health management app in addition to routine prenatal care. Researchers screen subjects strictly according to the exclusion and inclusion criteria and those who interested sign the informed consent. participants completed baseline questionnaire and dietary questionnaire at app under the instruction of researchers. Pregnant women come back for follow up-visit every 2 weeks until delivery. If anyone doesn't upload the weight data for a week and doesn't respond to the phone call from the researchers, she will be regarded as lost follow-up,the number of lost follow-up cases are supplemented by increasing the enrollment. Data analysis and result output finally. Besides, part of the study conducted in Beijing has some special points which don't exsit in large cohort study: participants equipment dynamic blood glucose monitor for glycemic control and their blood samples and stool samples will be collected at 24-28, 32 and 36 gestational weeks,respectively. Based on the description of weight gain range of pregnant women with normal blood glucose, the influence of weight gain on adverse pregnancy outcome was analyzed, and the recommended weight gain value for women with gestational diabetes was proposed in combination with Delphi expert consultation method.

Registry
clinicaltrials.gov
Start Date
March 24, 2020
End Date
June 30, 2022
Last Updated
4 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Pregnant women who have regular labor inspection and delivery in the labor inspection hospital;
  • Pregnant women with gestational diabetes diagnosed by OGTT at 24 to 28 weeks of pregnancy;
  • Singleton pregnancy;
  • Those who can skillfully use mobile phones and other electronic devices for scientific follow-up and voluntarily record their daily weight;
  • Voluntary signing of informed consent.

Exclusion Criteria

  • Patients with pre-pregnancy diabetes mellitus or abnormal OGTT screening in early pregnancy;
  • diabetic ketoacidosis,high blood sugar of high permeability anemia,leukemia, and lymphoma without clinical control.

Outcomes

Primary Outcomes

The incidence rate of infant outcomes

Time Frame: delivery

infant outcomes including SGA,neonatal hypoglycemia.

The incidence rate of pregnancy outcomes

Time Frame: delivery

pregnancy outcomes including preeclampsia, gestational hypertension.

Secondary Outcomes

  • the value of gestational weight gain during third trimester(from enrollment to delivery)

Study Sites (1)

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