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Comparing the Efficacy and Safety Between Continuous Subcutaneous Beinaglutide and CSII for Newly Diagnosed T2DM Patients

StatusRecruiting
PhaseNot applicable
Started
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Record status
This record was last updated May 2, 2025 (before its estimated September 2025 completion). Its status may not reflect the trial's current state.

Record History

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  1. Minor Secondary endpoints: details revised at 1 of 29 entriesv3
  2. Notable Trial status: Not Yet Recruiting to Recruitingv2 Show 10 more changesShow less
    • Enrollment target: 260 to 115
    • Primary completion date: Jun 30, 2021 to Sep 2025
    • Primary endpoint revised
    • Study sites: 9 to 16
    • Study completion date: Dec 30, 2021 to Dec 2025
    • Start date changed from estimate of Jul 1, 2019 to Jul 2, 2019
    • Eligibility criteria shortened, about 175 words
    • Secondary endpoints: 24 to 29
    • Study title shortened, about 7 words
    • Study description shortened, about 1 word
  3. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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The efficacy, safety and post-treatment disease control will be compared between groups of continuous subcutaneous Beinaglutide infusion and continuous subcutaneous insulin infusion (CSII) in adult patients with newly diagnosed type 2 diabetes.
Trial Details
NCT Number NCT03987308
Lead Sponsor Beijing Hospital
Conditions
(from sponsor)
Type 2 Diabetic Patients, T2DM (Type 2 Diabetes Mellitus), T2DM
Related terms Diabetes Mellitus, Type 2
Enrollment 115 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov