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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02520336
Other study ID # 7797
Secondary ID
Status Recruiting
Phase N/A
First received August 7, 2015
Last updated August 7, 2015
Start date July 2015

Study information

Verified date August 2015
Source Thomas Jefferson University
Contact n/a
Is FDA regulated No
Health authority United states: Thomas Jefferson university
Study type Interventional

Clinical Trial Summary

Assess postpartum diabetes screening in GDM patients with initiation of a reminder system in the postpartum period


Recruitment information / eligibility

Status Recruiting
Enrollment 78
Est. completion date
Est. primary completion date July 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria: GDM, english speaking -

Exclusion Criteria: Non english speaking. Younger than 18 years of age

Study Design

Allocation: Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Behavioral:
Reminder


Locations

Country Name City State
United States Thomas Jefferson University Hospital Philadelphia Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
Thomas Jefferson University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Postpartum Diabetes screening in GDM patients 1 year No
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