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NCT04206748 · ClinicalTrials.gov registry record · NA

iGlucose® Remote Patient Monitoring Device as an Adjunct to Routine Glucose Meter Devices for Glycemic Management and Control in Gestational Diabetes

A NA study of Gestational Diabetes and Type2 Diabetes, sponsored by The University of Texas Health Science Center, Houston.

Recruiting
Registry status
NA
Development phase
200
Enrollment target
1
Study location

NCT04206748 is a NA study of Gestational Diabetes and Type2 Diabetes that is actively recruiting participants, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 200 participants, below the 317-participant average among 41 other Gestational Diabetes trials with a reported enrollment target (37% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT04206748, a NA study of Gestational Diabetes and Type2 Diabetes, is actively recruiting participants, sponsored by The University of Texas Health Science Center, Houston.

RECRUITING
Registry status
NA
Development phase
200 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to investigate whether automation of glucose monitoring data to facilitate the total number of recommended and completed SMBG checks improve clinical outcomes for women living with gestational and type 2 diabetes during pregnancy? This is a RCT

Interventions

  • DEVICE iGlucose Smart Meter System
  • DEVICE Routine Care-RX meter

Study Locations (1)

Texas

  • The University of Texas Health Science Center at Houston - Houston

Trial Details

FieldValue
Enrollment Target 200 participants
Start Date 2019-11-12
Est. Completion 2022-11-01
Phase NA

What the Registry Record Tells You About NCT04206748

The ClinicalTrials.gov registry entry for NCT04206748 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 200 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 317-participant average among 41 other Gestational Diabetes trials with a reported enrollment target (37% lower). The listed sponsor is The University of Texas Health Science Center, Houston, which has 732 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Gestational Diabetes appearing as the primary indexed condition, and to 2 interventions - of which iGlucose Smart Meter System is the first listed.

NCT04206748 reports 1 study location spanning 1 distinct geographic area - top geographies include Texas.

Frequently Asked Questions

What is clinical trial NCT04206748 about?

NCT04206748 is a clinical study titled "iGlucose® Remote Patient Monitoring Device as an Adjunct to Routine Glucose Meter Devices for Glycemic Management and Control in Gestational Diabetes". The purpose of this study is to investigate whether automation of glucose monitoring data to facilitate the total number of recommended and completed SMBG checks improve clinical outcomes for women living with gestational and type 2 diabetes during pregnancy? This is a RCT

What is the current status of trial NCT04206748?

This trial is currently recruiting. It is a NA study. The enrollment target is 200 participants. The study started on 2019-11-12. Estimated completion is 2022-11-01.

What conditions does trial NCT04206748 study?

This clinical trial studies the following conditions: Gestational Diabetes, Type2 Diabetes, Pregnancy in Diabetic.

What interventions are being tested in trial NCT04206748?

The interventions under investigation include: iGlucose Smart Meter System (DEVICE), Routine Care-RX meter (DEVICE).

Who is sponsoring clinical trial NCT04206748?

This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04206748 being conducted?

This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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