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Search / Trial NCT06351176

Impact of Glycemic Control on Skeletal Outcomes in Adults With Type 1 Diabetes

Launched by CHU DE QUEBEC-UNIVERSITE LAVAL · Apr 2, 2024

Trial Information

Current as of July 26, 2025

Enrolling by invitation

Keywords

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Individuals with type 1 diabetes who have participated in the DenSiFy (Diabetes Spine Fractures) study (NCT04064437)
  • Inclusion Criteria:
  • Diagnosis of type 1 diabetes for at least 5 years;
  • Age 20 years and older.
  • Exclusion Criteria:
  • Pregnancy, delivery or breastfeeding in the past 6 months;
  • Conditions associated with bone disease (significant liver disease, intestinal malabsorption other than celiac disease, organ transplant, active cancer, rheumatoid arthritis, hyperthyroidism, hypothyroidism with abnormal TSH, hyperparathyroidism, hypoparathyroidism, hypogonadism, acromegaly, Cushing syndrome, adrenal insufficiency);
  • Any of these medications since the first DenSiFy study visit : biphosphonates, teriparatide, denosumab, calcitonin, glucocorticoids ≥ 7,5 mg prednisone/day or equivalency ≥ 3 months, aromatase inhibitors, antiandrogens, antiepileptic drugs, anticoagulants, thiazolidinediones;
  • Inability to consent.
  • Healthy controls who have participated in the DenSiFy (Diabetes Spine Fractures) study (NCT04064437)
  • Inclusion Criteria:
  • Age 20 years and older.
  • Exclusion Criteria :
  • * As above (as individuals with diabetes), and :
  • Diagnosis of diabetes or prediabetes;
  • Celiac disease;
  • Chronic kidney disease (CrCl \< 60 mL/min).

About Chu De Quebec Universite Laval

CHU de Québec-Université Laval is a leading academic health center in Canada, renowned for its commitment to advancing medical research and improving patient care. As a prominent clinical trial sponsor, it leverages its extensive network of healthcare professionals, researchers, and state-of-the-art facilities to conduct innovative clinical studies across various therapeutic areas. With a strong emphasis on collaboration and ethical standards, CHU de Québec-Université Laval aims to translate scientific discoveries into effective treatments, enhancing health outcomes for diverse populations.

Locations

Montréal, Quebec, Canada

Quebec City, Quebec, Canada

Patients applied

0 patients applied

Trial Officials

Claudia Gagnon, MD

Principal Investigator

CHU de Québec- Université Laval

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported