16 September 2026 editorial review · Trial
Argus 2.0 CGM adoption study: review notes
These notes document the scope actually reviewed, including source-access limits. They are not independent clinical certification or a guarantee that every claim was verified.
Read the trial evidence page →Baseline trial evidence review: A–H
Outcome: Expanded sparse summary/eligibility using current registry design, inclusion criteria and primary outcome; no efficacy inferred from registration.
Registry: NCT07425236. Registered endpoint checked: Quantity of Paired Argus and Reference Laboratory Blood Glucose Measurements During In-Clinic Visit (Day 1 (approximately 6 hours)); Quantity of Paired Argus and Dexcom Stelo CGM Data Points During Home-Wear Period (Day 1 through Day 15 (15 days)). Eligibility check: Registry age 18 Years to 75 Years; substantive diagnosis/stage, device and other inclusion restrictions were compared with the public eligibility summary. The registry remains the source for full exclusions. Limits: No usable primary abstract was independently recovered in this pass for this record. Protocol/design wording was assessed; any existing detailed sponsor, conference or historical outcome claims require their cited source and were not independently certified through full-text review.