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NCT Number: NCT06826547

Optimization of Basal Insulin During Ramadan Fasting in Type 2 Diabetic Patients: Comparison Between DAR Recommendations and the Carbohydrate Fasting Test & Metabolic and Inflammatory Consequences

Ramadan, a fasting period observed by many Muslim patients, poses a significant challenge for glycemic management in diabetics. During this month, abstinence from food, water, and medication from dawn to dusk leads to significant glycemic fluctuations. Inadequate insulin dose management can cause acute complications such as hypoglycemia, hyperglycemia, ketosis, or hyperosmolar states. In 2021, the Diabetes and Ramadan (DAR) guidelines provided recommendations for adjusting insulin doses, taking into account changes in circadian rhythms and patients' dietary habits. However, these standardized recommendations may not be suitable for everyone. A personalized alternative, the Carbohydrate Fasting Test (CFT), allows for the assessment of individual basal insulin needs through a controlled fast excluding carbohydrates for 24 hours. Comparing these two approaches could provide valuable insights into their relative effectiveness, particularly in terms of safety and quality of life for patients.

Moreover, diabetes can be influenced by fasting, with potentially beneficial effects on inflammation and metabolism.

This study aims to determine which of these two methods optimizes glycemic control and to assess the variations of inflammation markers before and after Ramadan fasting. The results could be integrated into future clinical practices to improve diabetes management during Ramadan. We aim to compare the effectiveness and safety of basal insulin dose adjustments according to DAR 2021 guidelines versus the Carbohydrate Fasting Test (CFT) and to analyze the impact on the quality of life of diabetic patients. This is a prospective, longitudinal, randomized, interventional study including 60 Type 2 diabetic patients, aged 18 to 70 years old, on insulin therapy for at least 6 months. All participants intend to fast during Ramadan and are at low to moderate risk according to the IDF-DAR score (≤6).

Eligible patients will be randomly assigned into two groups:

DAR Group: Insulin dose adjustments according to DAR 2021 recommendations. CFT Group: Personalized insulin adjustments based on a Carbohydrate Fasting Test conducted before Ramadan.

Protocol:

Initial assessment will be Clinical ( Weight, BMI, blood pressure) and biological (Fasting glucose, HbA1c, fructosamine and inflammatory markers ( Interleukin 6 and TNF alfa)).

During Ramadan, weekly glycemic monitoring will be conducted to track blood sugar levels. Any complications will be recorded, and insulin dose adjustments will be made remotely if necessary to ensure optimal glycemic control.

In the last week of Ramadan, a final clinical assessment will be performed, including measurements of weight, BMI, and blood pressure. A biological assessment will also be conducted to measure fructosamine levels and inflammatory markers ( Interleukin 6 and TNF alfa).

Two months after Ramadan, fasting glucose and HbA1c levels will be re-evaluated to assess long-term glycemic control. The study will also analyze the impact on glycemic regulation, anthropometric parameters, and overall quality of life using the SF-12 questionnaire.

In conclusion, this project aims to identify the most effective method for adjusting basal insulin doses during Ramadan, contributing to optimal Type 2 diabetes management and to assess the variations of inflammation markers before and after Ramadan fasting.

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This study is active but is not currently recruiting participants.

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Early Phase 1

Primary location

La Rabta Hospital , Endocrinology Department

Tunis, 1000, Tunisia

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults aged 18 to 70 years with Type 2 diabetes on a basal insulin regimen (NPH, Detemir, or Glargine) with or without 1 to 2 boluses of rapid-acting insulin.
  • Diabetes duration of at least 2 years and insulin therapy for at least 6 months.
  • Patients wishing to fast during Ramadan and having provided informed consent.
  • Low risk of complications according to the IDF-DAR 2021 risk score or moderate risk for patients who insist on fasting.

Non-Inclusion Criteria:

  • High-risk patients according to IDF-DAR 2021 score >6, including those with:
  • Severe renal impairment
  • Cognitive dysfunction or frailty
  • Unrecognized hypoglycemia
  • Unstable cardiovascular disease
  • Pregnancy
  • Type 1 diabetes
  • Type 2 diabetes patients on sulfonylureas or related medications

Exclusion criteria

  • Patients who did not follow the study protocol regarding insulin dose adjustments and capillary blood glucose (CBG) self-monitoring.
  • Fasting discontinuation without medical advice.
  • Severe complications requiring fasting cessation.
  • Patients who withdrew their informed consent.

Treatment and study plan

Adjustment of insulin doses DAR

Drug

Patients will be hospitalized at La Rabta Hospital from February 15 to February 28, 2025 for clinical (weight, BP, SF-12), biological (HbA1c, lipid profile) assessments and inflammatory markers (Interleukin 6 and TNF alfa) DAR Group: Insulin will be adjusted per DAR 2021 guidelines. Patients will track insulin doses, glycemic cycles, hypoglycemia episodes, fasting interruptions, and hospital visits in a dedicated log. They will receive weekly calls for insulin adjustments and continuous support.

During the last week of Ramadan, clinical and biological data including inflammatory markers will be collected. Two months post-Ramadan, HbA1c, fasting glucose, and lipid profile will be reassessed to evaluate glycemic control.

Adjustment of insulin doses CFT

Drug

Patients will be hospitalized at La Rabta Hospital from February 15 to February 28, 2025 for clinical (weight, BP, SF-12) and biological (HbA1c, lipid profile) assessments and inflammatory markers (Interleukin 6 and TNF alfa) .

CFT Group: Insulin adjusted after a Carbohydrate Fasting Test. Patients will track insulin doses, glycemic cycles, hypoglycemia episodes, fasting interruptions, and hospital visits in a dedicated log. They will receive weekly calls for insulin adjustments and continuous support.

During the last week of Ramadan, clinical and biological data including inflammatory markers will be collected. Two months post-Ramadan, HbA1c, fasting glucose, and lipid profile will be reassessed to evaluate glycemic control.

Primary outcomes

  1. fructosamine levels

    Time frame: up to 6 weeks

    Fructosamine variation 15 days before & the last week of Ramadan

  2. Interleukin-6 levels

    Time frame: up to 6 weeks

    variation during the fast of Ramadan 15 dayd before and at the Last week of Ramadan

  3. Hypoglycemia

    Time frame: up to one month

    Frequency of hypoglycemic episodes

  4. glycemic auto-monitoring

    Time frame: up to one month

    Percentage of blood glucose values meeting target levels during the month of Ramadan

  5. HbA1c levels

    Time frame: up to 6 weeks

    HbA1c variation before and after Ramadan 15 days before & 2 months after Ramadan

  6. TNF-alfa levels

    Time frame: up to 6 weeks

    Variation during fasting Ramadan 15 days before and at the Last week of Ramadan

Secondary outcomes

  1. Body mass index

    Time frame: up to 6 weeks

    Body mass index variation : Before and at the Last week of Ramadan

  2. Quality of life of patients

    Time frame: up to 6 weeks

    Quality of life of patients assessed using the Medical Outcomes Study Short-Form General Health Survey (SF-12) questionnaire in its validated Tunisian dialect version.

    Before and at at the last week of Ramadan Higher score means a better quality of life.

  3. waist circumference

    Time frame: up to 6 weeks

    variation of waist circumference: Before and at the Last week of Ramadan

  4. Blood pressure

    Time frame: up to 6 weeks

    Variation of blood pressure : Before and at the Last week of Ramadan

Sponsors and collaborators

Lead sponsor

University Tunis El Manar

Other

Collaborators

  • Hopital La Rabta

Registry information

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Feb 14, 2025
Registry last updated
Mar 10, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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