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COMPLETED NA

Evaluating the Feasibility of Using M-Health to Improve Serum Glucose Logs

NCT03340311 · View on ClinicalTrials.gov ↗

Study Summary

Gestational diabetes mellitus (GDM) can cause adverse outcomes for the mother and fetus due to hyperglycemia. The purpose of this study is to evaluate the feasibility of improving pregnant women's glucose logs using a Bluetooth enabled glucose monitor and associated mobile health application and to assess their satisfaction with using mobile health technology.

Interventions

  • DEVICE iHealth Wireless Smart Gluco- Monitoring System (BG5)

Study Locations (1)

Virginia

  • University of Virginia Maternal Fetal Medicine Clinic — Charlottesville

Trial Details

FieldValue
Enrollment Target 8 participants
Start Date 2017-11-01
Est. Completion 2018-04-28
Phase NA

Sponsor

Leslie Balcazar De Martinez

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03340311

The ClinicalTrials.gov registry entry for NCT03340311 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 8 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Leslie Balcazar De Martinez, which has 1 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Gestational Diabetes Mellitus appearing as the primary indexed condition, and to 1 intervention — of which iHealth Wireless Smart Gluco- Monitoring System (BG5) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT03340311 reports 1 study location spanning 1 distinct geographic area — top geographies include Virginia. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT03340311 about?

NCT03340311 is a clinical study titled "Evaluating the Feasibility of Using M-Health to Improve Serum Glucose Logs". Gestational diabetes mellitus (GDM) can cause adverse outcomes for the mother and fetus due to hyperglycemia. The purpose of this study is to evaluate the feasibility of improving pregnant women's glucose logs using a Bluetooth enabled glucose monitor and associated mobile health application and to ...

What is the current status of trial NCT03340311?

This trial is currently completed. It is a NA study. The enrollment target is 8 participants. The study started on 2017-11-01. Estimated completion is 2018-04-28.

What conditions does trial NCT03340311 study?

This clinical trial studies the following conditions: Gestational Diabetes Mellitus. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03340311?

The interventions under investigation include: iHealth Wireless Smart Gluco- Monitoring System (BG5) (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03340311?

This trial is sponsored by Leslie Balcazar De Martinez, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03340311 being conducted?

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

Related

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