Postpartum Diabetes Screening in Women With Gestational Diabetes

NCT ID: NCT02520336

Last Updated: 2015-08-11

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

78 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-07-31

Brief Summary

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

Detailed Description

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Conditions

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Diabetes, Gestational

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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active management

Laboratoy test request given postpartum with phone reminder prior to test

Group Type EXPERIMENTAL

Reminder

Intervention Type BEHAVIORAL

Routine care

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Reminder

Intervention Type BEHAVIORAL

Eligibility Criteria

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Exclusion Criteria

\-
Minimum Eligible Age

18 Years

Maximum Eligible Age

50 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Thomas Jefferson University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Thomas Jefferson University Hospital

Philadelphia, Pennsylvania, United States

Site Status RECRUITING

Countries

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United States

Facility Contacts

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Adeeb Khalifeh, MD

Role: primary

Other Identifiers

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7797

Identifier Type: -

Identifier Source: org_study_id

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