NCT07891156Toboroz2/3. fázis
Lean Mass Changes With Semaglutide in Adults With Type 1 Diabetes and Overweight/Obesity.
Changes to Body Composition With Semaglutide vs. Placebo in Adults With Type 1 Diabetes and Overweight/Obesity: a Double-blinded, Randomized, Parallel Controlled Trial
Forrás: ClinicalTrials.gov · Utoljára frissítve: 2026. okt. 23.
Rövid összefoglaló (regiszter, angolul)
The goal of this 24 week double-blinded, randomized, parallel controlled clinical trial is to learn how semaglutide affects body composition in adults with type 1 diabetes and overweight/obesity. The main question to answer is: What effect does Semaglutide have on body composition in adults with type 1 diabetes and overweight/obesity compared to a placebo? Around 40 participants will: * Be randomly assigned to receive semaglutide or a placebo. * Self-administer the treatment drug once per week for 24 weeks. * Complete a series of tests, measurements and questionnaires throughout the study duration. * Attend a remote follow-up visit 4 weeks after the treatment is complete.
- Állapot (regiszter)
- Toboroz
- Fázis (regiszter)
- 2/3. fázis
- Vizsgálattípus
- Beavatkozással járó
- Résztvevők száma
- 40 (tervezett)
- Első benyújtás
- 2026. aug. 9.
- Kezdés
- 2026. okt. 13.
- Elsődleges befejezés
- 2028. szept. 1.
- Fő szponzor
- McGill University Health Centre/Research Institute of the McGill University Health Centre
- Betegségek
- 1-es típusú cukorbetegség, Elhízás
- NCT-szám
- NCT07891156
Mit vállalsz
- Vizsgálat típusa: Beavatkozással járó · 2/3. fázis
- Tervezett résztvevők: 40
- 2026. okt. 13. és az elsődleges befejezés (2028. szept. 1.) között
- 1 helyszín, 1 országban
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Korábbi kezelés
- Prior hypersensitivity reaction to GLP1-RA (glucagon-like-peptide-1 receptor agonist)
- Any prior diagnostic history of eating disorder or suicidal attempts, or feelings of suicidal thoughts or behaviours in the last month**
Más betegség
- Pre-existing conditions limiting physical activity, specifically inability to walk for 6 minutes.
- Active proliferative diabetic retinopathy requiring surgery or laser/injectable therapy within the last 3 months.
- *If a history of proliferative retinopathy is present within the last year, written permission from the eligible participant's ophthalmologist or optometrist is required*
- History of bariatric surgery
- Personal history of acute/chronic pancreatitis or gallstone disease without cholecystectomy.
- Personal or family history of medullary thyroid cancer or multiple endocrine neoplasia type 2.
- Unstable angina, or myocardial infarction/ cardiovascular surgery / coronary stenting in the last month.
- Any serious medical or psychiatric illness likely to interfere with study participation as per the judgment of the investigator (e.g. cirrhosis, active cancer, decompensated schizophrenia).
Laborértékek
- HbA1c (glycated hemoglobin) ≥ 10% within the last 3 months.
- Severe hypoglycemic episode within the last 3 months, defined as an event where glycemia was < 4 mmol/L, resulting in seizure, loss of consciousness, or need for third-party assistance in treatment.
- Severe impairment of renal function with eGFR <30 mL/min/1.73 m2 (using CKD-EPI formula), measured within the last 12 months.
Egyéb
- Current use of non-insulin anti-hyperglycemic agents within the last month.
- Diabetic ketoacidosis (DKA) within the last 3 months (DKA refers to the need to present to medical attention and the requirement of intravenous insulin due to ketones)
- Use of supraphysiological doses of glucocorticoids in the last 3 months, and/or expected use at some point in the next 6 months.
- Planned or ongoing pregnancy
- Breastfeeding individuals
- Clinically significant gastroparesis, defined as persistent symptoms despite pharmacotherapy such as domperidone.
Kiket keres a vizsgálat
- Age 18-65 years old
- Clinical diagnosis of T1D (type 1 diabetes) for ≥ 1 year, as per clinician judgement.
- BMI (Body mass index) ≥ 27 kg/m2
- Use of multi-daily injections or insulin pump therapy.
- Use of CGM (continuous glucose monitoring).
- Agreement to the use of a highly effective method of birth control in persons of child-bearing age (if sexually active) and active avoidance of pregnancy during the trial. Child-bearing potential refers to participants of the female sex post-menarche who have not reached menopause or have a disclosed medical condition causing sterility (e.g. hysterectomy). Post-menopausal state refers to the absence of menses for 12 months without any alternative cause.
- Diabetic retinopathy assessment performed within the last 2 years, as per participant history.
Életkor a regiszterben: 18 év – 65 év · Nem: nők és férfiak · Egészséges önkénteseket nem fogad
Helyszínek (1)
Helyszínek a regiszter sorrendjében. Ha a profilodba mented a városodat, távolság szerint rendeződnek.
| Helyszín | Város | Ország | Helyszín állapota |
|---|---|---|---|
| Research Institute of the McGill University Health Centre Royal Victoria Hospital | Montreal | Kanada | Toboroz |
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