Continuous Glucose Monitoring By DExcom iN PEople Followed for Type 2 DIabeTes on Insulin Therapy in the Kingdom of Saudi Arabia (BENEFIT-KSA)

Continuous Glucose Monitoring By DExcom iN PEople Followed for Type 2 DIabeTes on Insulin Therapy in the Kingdom of Saudi Arabia: The "BENEFIT-KSA" Study

This study aims to understand how using real-time continuous glucose monitoring (RT-CGM) can help people with Type-2 diabetes on insulin in Saudi Arabia.

Study Overview

• Status: Active, not recruiting
• Conditions: Type 2 Diabetes on Insulin
• Intervention / Treatment: Device: Real-Time Continuous Glucose Monitoring

Detailed Description

This study aims to understand how using real-time continuous glucose monitoring (RT-CGM) can help people with type 2 diabetes (T2DM) on insulin in Saudi Arabia better manage their blood sugar levels. Diabetes is a growing health problem in the country, affecting nearly 1 in 4 adults over 30. Many people struggle with managing their condition, leading to serious health complications and rising healthcare costs. This study will recruit adults with T2DM who are using either basal insulin (one or two daily basal injections) or are on intensive insulin insulin therapy (IIT-multiple daily injections).

Each participant will wear a RT-CGM device for 24 weeks, with an optional 30-day extension where participants will wear a blinded CGM to observe what happens when RT-CGM is stopped in this population. The CGM device tracks blood sugar levels continuously, helping both patients and doctors see patterns and make better treatment decisions. The main purpose of the study is to see if RT-CGM use helps lower HbA1c (a key marker of long-term blood sugar control) after 12 weeks. The study will also look at other outcomes, such as: Changes in HbA1c after 24 weeks; reduction in low blood sugar episodes; improvements in lifestyle habits like diet and exercise; changes in medication; effects on heart health and healthcare usage; and patient-reported experiences and satisfaction.

The study is designed to be safe, with risks similar to regular diabetes care. The information gained could help improve diabetes treatment in Saudi Arabia and support updates to local clinical guidelines for this patient population. The researchers believe that CGM can reduce HbA1c levels, empower patients to improve blood sugar control and reducing complications for people living with type 2 diabetes.

• Study Type: Interventional
• Enrollment (Estimated): 200
• Phase: Phase 4

Contacts and Locations

Study Locations

• Saudi Arabia
  • Riyadh, Saudi Arabia
    • King Fahad Medical City

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

- 1. Age of at least 18 years at time of screening. 2. Type 2 diabetes and on either intensive insulin therapy (IIT) or basal insulin therapy for ≥6 months prior to entry.

i. IIT: Defined as basal insulin + ≥2 daily bolus injections of rapid acting insulin or ≥2 injections per day of premixed insulin (e.g. 70/30 or 50/50).

ii. Basal: Defined as ≤2 injections per day of basal insulin only and not planning to start rapid acting or premixed insulin in the next 6 months.

3. Screening HbA1c ≥8% at enrollment (by local lab at time of screening). 4. Assessment by clinician that participant is thought to be able and willing to wear, and motivated to engage with, a CGM device.

5. No personal real-time or intermittent scanned (Flash) CGM use, or use of a glucose biosensor 3 months prior to enrolment.

6. Stable diabetes, lipid lowering, and anti-obesity medication regimen (medication classes) and dose (equivalent dose if diabetes/anti-obesity-specific, or lipid-lowering medication has been changed within same medication class) for 3 months prior to enrollment.

Note: Changes ≤ 10% in total daily doses of insulin in the 3 months prior to enrollment are permitted.

7. Willing to follow study procedures as defined within the study protocol according to the judgement of the study physician.

8. Investigator believes that the participant has the cognitive capacity to provide informed consent, can successfully and safely use CGM, and is capable of adhering to the protocol and completing the study.

Exclusion Criteria:

• 1. Diagnosis of type 2 diabetes not on insulin or diagnosis of type 1 diabetes 2. Any surgical procedure for weight loss within the year prior to enrollment or plans for undergoing such bariatric surgery during the study.

  3. Concomitant disease or condition that in the opinion of the investigator may compromise participant safety including but not limited to: solid organ transplant, cystic fibrosis, severe mental illness, a diagnosed or suspected eating disorder or any uncontrolled long term medical condition that would interfere with study related tasks or visits.

  4. Use of medications known to exacerbate hyperglycemia (current or for more than 14 days in the past 3 months), including corticosteroids (oral and injectable) or certain psychotropics (antipsychotics, e.g., clozapine, olanzapine, risperidone, and quetiapine).

  5. Known severe allergy to medical grade adhesives or a serious skin condition that precludes use of the CGM.

  6. Currently pregnant, planning to become pregnant, or breastfeeding 7. End stage renal disease currently managed by dialysis or anticipating initiating dialysis during the next 6 months, OR eGFR <30.

  o Baseline blinded CGM data collection can be initiated prior to the lab result being available but lab result must be available prior to initiation to verify eligibility.

  8. Anticipated acute uses of glucocorticoids (oral, injectable, or IV) that will affect glycemic control and impact HbA1c.

  9. Current or planned use of hydroxyurea. 10. Presence of a hemoglobinopathy or other condition that is expected to affect the measurement of HbA1c in the judgment of the investigator.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Supportive Care
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: real-time continuous glucose monitoring (RT-CGM); 24 weeks of real-time continuous glucose monitoring (RT-CGM)	Device: Real-Time Continuous Glucose Monitoring; real time continuous glucose monitoring utilizing a CGM

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in HbA1c	Change in HbA1c from baseline to week 12	12 weeks

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Change in HbA1c and CGM derived metrics	Change in HbA1c from baseline to week 24	Measurement at 12 weeks & 24 weeks

Collaborators and Investigators

• Sponsor: DexCom, Inc.

Study record dates

Study Major Dates

• Study Start (Actual): November 24, 2025
• Primary Completion (Estimated): November 2, 2026
• Study Completion (Estimated): December 31, 2026

Study Registration Dates

• First Submitted: May 18, 2026
• First Submitted That Met QC Criteria: May 18, 2026
• First Posted (Actual): May 22, 2026

Study Record Updates

• Last Update Posted (Actual): May 22, 2026
• Last Update Submitted That Met QC Criteria: May 18, 2026
• Last Verified: May 1, 2026

More Information

Terms related to this study

• Keywords: diabetes; insulin; type-2
• Additional Relevant MeSH Terms: Endocrine System Diseases; Metabolic Diseases; Glucose Metabolism Disorders; Hyperinsulinism; Nutritional and Metabolic Diseases; Diabetes Mellitus; Insulin Resistance
• Other Study ID Numbers: PTL-1000518

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No