CGM Experience, Preferences & Blood Glucose Parameters

Sponsor
Getz Pharma
Study ID
NCT07607015
Status
Not Yet Recruiting

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Conditions

  • Diabete Mellitus
  • Gestational Diabetes
  • Pre Diabetes
  • Type2diabetes
  • type1diabetes

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • CGM — DEVICE
    Comparison of 2 devices by HCP

Study Details

This is an open-label, prospective, multicenter observational study designed to evaluate the perceived benefits, device experience, preference, and glucose-related parameters associated with the Instara-1 Continuous Glucose Monitoring device. The study will include patients with diabetes and healthcare professionals. Patients will use Instara- 1 and will be followed up to assess device experience, glucose parameters, and diabetes-related quality of life. Healthcare professionals will evaluate device experience and preference, including comparison with FreeStyle Libre 2.

Key Dates

First listed
May 26, 2026
Start date
Sep 10, 2026
Status verified
May 2026
Primary completion
Aug 10, 2027
Completion
Aug 10, 2027

Study Design

Enrollment
75 participants (estimated)

Arms

  • Arm: Instara-1 CGM
    Participants in this arm will use the Instara-1 Continuous Glucose Monitoring . Patients will be followed for device experience, perceived benefits, preference, glucose-related parameters, and diabetes-related quality of life. Healthcare professionals will assess device experience and preference, including comparison with FreeStyle Libre 2 where applicable.

Primary Outcome Measure

Benefit, device experience and preference of continuous glucose monitoring by patients and HCPs [ Time Frame: From enrollment to the end of treatment at 3 weeks. ]

Central Contacts

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