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Postprandial Glucose Handing in Contraceptive and IUD Users

Exploring the Effect of Hormonal Contraceptives on Postprandial Glucose Handling in Young Healthy Females

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07169591
Acronym
HCPG
Enrollment
54
Registered
2025-09-12
Start date
2025-10-01
Completion date
2026-10-31
Last updated
2025-09-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Glucose Homeostasis

Keywords

Glucose, Insulin, Female Health, Hormonal Contraceptive, Intrauterine Device, Oral Contraceptive Pill

Brief summary

Goals: The long-term use of hormonal birth control has been shown to effect glucose handling, or blood sugar regulation, and potentially lead to insulin resistance which increases a person's risk for metabolic diseases such as type 2 diabetes. The goal of this study is to investigate how the body handles glucose, in three groups of young, healthy females: NAT (naturally cycling, or not using hormonal birth control), OCP (taking a birth control pill), and IUD (using an intrauterine device). Objectives: We will investigate if the body's ability to handle glucose differs between these groups. We will also explore if these differences are linked to the levels of primary sex hormones in females, estrogen and progesterone, and if the synthetic versions produced by hormonal birth control have the same negative effect. We will use an oral glucose tolerance test to investigate these potential differences, having participants drink a 75 gram glucose beverage and taking blood samples every 15-30 minutes for a 2-hour timespan. These blood samples will be used to measure glucose and insulin levels in the blood to determine any changes that occur in the body in response to glucose.

Detailed description

Insulin resistance is a common metabolic condition, and is considered a primary risk factor for the development of type 2 diabetes (T2D). As the prevalence of T2D continues to rise, particularly among premenopausal females (18-45 years), it is imperative to conduct additional research in this area. Fluctuations in primary sex hormones in females have been shown to modulate risk for developing impaired glucose tolerance, however, research in this area as well as work investigating synthetic versions of these hormones for OCP and IUD users remains unclear. It is crucial to investigate how hormonal contraceptives can alter glucose tolerance in young, otherwise healthy females, and what downstream effects contraceptives could have later in life.

Interventions

Standard oral glucose tolerance test with blood draws every 15-30 minutes for a 2-hour span

Sponsors

McMaster University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* Within 18-45 years * BMI between 18.5 and 30.0 kg/m2 * Weight stable for the past 6 months (± 2kg) * VO2peak values within a below average to above average rangea * Fasting blood glucose \<6.0 mMb * Resting blood pressure \<140/90 mmHg NAT females: • Regular menstrual cycle for \> 6 months (defined as a cycle length of 21-35 days) OCP users: * Use of combined OCPs as prescribed for \> 3 months * Second generation levonorgestrel drugs only * Monophasic formulations only (Alesse, Alysena, Audrina, Aviane, Min-Ovral, Ovima, or Portia) IUD users: * Insertion of IUD no fewer than 3 months prior to beginning of study * Hormonal, levonorgestrel-releasing IUD (Kyleena or Mirena)

Exclusion criteria

* Smoking * Diabetes, cancer, or other metabolic disorders * Cardiac or gastrointestinal problems * Infectious disease * Barium swallow or nuclear medicine scan in the previous 3 weeks * Pregnant or breastfeeding * Diagnosis of polycystic ovary syndrome * Endometriosis * Use of emergency contraception (e.g., Plan B) within the previous 3 months NAT females: • Use of any type of hormonal contraceptive in the previous 3 months OCP users: * Not using OCP as prescribed (e.g. missing doses or taking drug inconsistently) * Use of OCP for longer than 3 years. IUD users: * Insertion of Kyleena IUD longer than 2 years. * Insertion of Mirena IUD longer than 4 years.

Design outcomes

Primary

MeasureTime frameDescription
Glucose tolerance2 hoursA 2-hour oral glucose tolerance test will be performed in fasted individuals

Secondary

MeasureTime frameDescription
Glucose and lipid metabolitesTimepoints: 0 minute, 15 minute, 30 minute, 45 minute, 60 minute, 90 minute, 120 minutePeak concentration of whole blood glucose

Other

MeasureTime frameDescription
Hormone availabilityFasting (0 min timepoint)Concentration of 17b estradiol (endogenous estrogen)

Countries

Canada

Contacts

Primary ContactKirsten E Bell, Ph.D.
bellke3@mcmaster.ca905-525-9140

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026