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Semaglutide GLP1 Agonists With Degludec Basal-bolus Insulin in Early Type 1 Diabetes to Basal-bolus
A Randomized Clinical Trial Comparing Semaglutide GLP1 Agonists With Degludec Basal-bolus Insulin in Early Type 1 Diabetes
Lead sponsor
Assets
GLP-1 / incretin class catch-all / Semaglutide
Listed sites
0
Recruiting sites
—
Enrollment
120
estimated
Study population
Type 1 diabetes
Key I/E criterion
—
Primary endpoint
•HbA1c, change (HbA1c, change)
Identifiers
Registered as
Timeline
Milestones
Assets
Investigational agents
Study populations
Who this study enrolls
Eligibility
Who can enroll
Inclusion criteria
early diagnosed type 1 diabetic patients were diagnosed in the last 6 months age of two groups: from 18-35 years basal-bolus insulin patients
Exclusion criteria
no oral hypoglycemic drugs no pregnancy no hypoglycemic drugs or immunosuppressant no history of diabetic ketoacidosis
Endpoints (2)
What's being measured
Protocol endpoints and posted registry outcome measures, grouped into outcome categories. Composite endpoints show their component event types. Standard codes (LOINC, SNOMED CT) are shown where available.
Coverage by outcome category
Weight & body composition
1 endpointthe change in weight after follow up of one year
Time frame:one year
Body weight, absolute change (kg)
change from baseline, improvement
Glycemic / diabetes
1 endpointchange in HA1c and mounts of insulin of basal and bolus which will be taken daily is the same or decreased after one year of follow up
Time frame:Time Frame: one year
HbA1c, change
change from baseline, improvement
componentsHbA1c, change
LOINC 4548-4
Publications (2)
Bibliography
Records linked to this trial through ClinicalTrials.gov references, PubMed NCT search, and curated study seeds. 'Canonical' marks design/result papers; others are registry references or candidates.
Registry references + supporting bibliography
- Advanced pharmaceutical bulletin2024 Jul (month)PMID39206389doi:10.34172/apb.2024.040via clinicaltrials gov reference derived + pubmed nct search
- Molecular cancer therapeutics2016 Jun (month)PMID27048952doi:10.1158/1535-7163.MCT-15-0815via CT.gov reference
Provenance
Sources
Trial facts come from public ClinicalTrials.gov records. Endpoint categories are Delfa's classification of those records, not a ClinicalTrials.gov field. All figures reflect the July 1, 2026 snapshot.