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NCT05633628Recruiting

Periodic Continuous Glucose Monitoring in Patients With Type 2 Diabetes

Periodic Continuous Glucose Monitoring to Support a Person-centered Approach During Diabetes Consultations in Patients With Type 2 Diabetes- A Randomised Controlled Study

Source: ClinicalTrials.gov · Last updated 29 Apr 2026

Brief summary (registry, in English)

The aim of this randomised controlled trial is to investigate the effectiveness of periodic CGM (continuous glucose monitoring) to support a person-centered approach versus self-monitoring of blood glucose (SMBG) in adults with type 2 diabetes on glucose control and patient reported outcomes.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
400 (estimated)
First submitted
21 Nov 2022
Start date
1 Feb 2023
Primary completion date
Dec 2026
Lead sponsor
Sophiahemmet University
NCT number
NCT05633628

What you commit to

  • Study type: Interventional
  • Planned participants: 400
  • From 1 Feb 2023 to the primary completion date, Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Planned or currently using weight reduction medications, programs, or surgery

Other illness

  • Active malignancy or under investigation for malignancy
  • Severe visual impairment
  • Eating disorders

Lab values

  • Renal disease with estimated glomerular filtration rate (eGFR) \<45 mL/ min/1.73 m2
  • Severe skin allergy that inhibits the use of a continuous glucose monitoring device

Other

  • Prandial insulin
  • Pregnancy or planning pregnancy during the study
  • Breastfeeding
  • Glucocorticoids (systemic)
  • Cognitively or psychologically unable to participate and read instructions
  • Enrolled in other clinical trials

Who the study is looking for

  • Adults aged 18-80 years
  • Type 2 diabetes with a duration of \> 6 months
  • HbA1c 45-70 mmol/mol
  • Have a smartphone
  • Experience of self-monitoring of blood glucose prior to the study start

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Sophiahemmet University
Coordinator of this site? Confirm its status
StockholmSwedenRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.