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Search / Trial NCT06619301

RCT Glargine vs NPH for Treatment of DM in Pregnancy

Launched by LOYOLA UNIVERSITY · Sep 26, 2024

Trial Information

Current as of November 10, 2025

Recruiting

Keywords

Glargine Nph Hypoglycemia

ClinConnect Summary

This clinical trial is studying two types of insulin, Glargine and NPH, to see which one works better for managing diabetes during pregnancy. If you are pregnant and have been diagnosed with Type 2 diabetes or gestational diabetes that requires insulin treatment, you may be eligible to participate. To join, you need to be at least 18 years old, start insulin before 34 weeks of pregnancy, and have established prenatal care by 14 weeks.

If you take part in this study, you will be randomly assigned to receive either Glargine or NPH insulin. The goal is to find out which insulin helps manage blood sugar levels more effectively and safely during pregnancy. It's important to note that this study is currently recruiting participants, and if you have any allergies to insulin, are under 18, or are managing your diabetes with diet or oral medications, you won’t be able to participate. Your involvement could help improve diabetes care for pregnant women in the future!

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • Patient requiring initiation of insulin therapy for Gestational Diabetes Mellitus or Type 2 Diabetes Mellitus in pregnancy
  • At least 18 years old
  • Insulin started prior to 34 weeks gestation
  • Established prenatal care by 14 weeks gestation
  • Exclusion Criteria:
  • Those under the age of 18 years old
  • Those unable to consent in english
  • Allergy to insulin
  • Controlled with only diet modification or the use of oral antihyperglycemics
  • Has diagnosis of Type 1 Diabetes Mellitus
  • Receiving insulin through an insulin pump

About Loyola University

Loyola University is a prestigious academic institution dedicated to advancing medical research and clinical innovation. As a sponsor of clinical trials, Loyola University leverages its extensive resources, expert faculty, and commitment to ethical research practices to explore new therapeutic interventions and improve patient outcomes. The university fosters a collaborative environment that brings together multidisciplinary teams to conduct rigorous studies across various fields of medicine, ensuring that the findings contribute to the broader healthcare community and enhance evidence-based practices. Through its dedication to scientific excellence and community health, Loyola University remains at the forefront of clinical research initiatives.

Locations

Maywood, Illinois, United States

Patients applied

0 patients applied

Trial Officials

Joana Lopes Perdigao, MD

Principal Investigator

Loyola University

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported