Actively Recruiting

Age: 18Years +
FEMALE
Healthy Volunteers
NCT06147466

Time Spent In Target Glucose Range in Women With T2D Diabetes in Pregnancy

Led by Mount Sinai Hospital, Canada · Updated on 2024-03-20

50

Participants Needed

1

Research Sites

169 weeks

Total Duration

On this page

Sponsors

M

Mount Sinai Hospital, Canada

Lead Sponsor

U

University of Manitoba

Collaborating Sponsor

AI-Summary

What this Trial Is About

Prospective cohort study to determine to what extent women with type 2 diabetes are achieving the time in the target range outlined for women with type 1 diabetes (70-140 mg/dl or 3.5-7.8 mmol/l), overall and by trimester, by standard CGM measures and functional data analysis

CONDITIONS

Official Title

Time Spent In Target Glucose Range in Women With T2D Diabetes in Pregnancy

Who Can Participate

Age: 18Years +
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Women with type 2 diabetes diagnosed before pregnancy or before 20 weeks gestation confirmed by HbA1c >6.5%, fasting glucose 67.0, or 2-hour glucose 611.1 on a 75g OGTT
  • Pregnancy of 14 weeks gestation or less
  • Age 18 years or older
  • Willing to use study devices at least 10 days per trimester
  • Able to provide informed consent
  • Have access to email
Not Eligible

You will not qualify if you...

  • Non-type 2 diabetes diagnosis
  • Current use of drugs interfering with glucose metabolism like high dose systemic corticosteroids
  • Known or suspected allergy to insulin
  • Nephropathy with eGFR <30, severe autonomic neuropathy, or uncontrolled gastroparesis likely interfering with the study
  • Severe visual or hearing impairment affecting treatment compliance
  • Inability to communicate effectively in English
  • Any condition judged by the investigator to interfere with study conduct or results

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

Mount Sinai Hospital

Toronto, Ontario, Canada

Actively Recruiting

Loading map...

Research Team

D

Denice Feig, MD, MSc, FRCPC

CONTACT

S

Silva Darrouj, HBSc

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here