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Completed

NCT Number: NCT03489031

Basal Insulin And Compensation Glycemic In Diabetic Patients In Basal Bolus Outpatient.

Multicentric, observational, cross-sectional study in Italy. The aims are to evaluate the basal/total ratio of daily insulin dose (b/T) in diabetic outpatients type 1 (T1) and type 2 (T2) on basal-bolus regimen, by investigating whether there is a relationship with HbA1c and episodes of hypoglycemia.

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Key information

About this study

The study was commissioned by the Italian Association of Clinical Endocrinologists (Associazione Medici Endocrinologi - AME) and approved by the Ethical Committee of Cuneo Hospital (BASAL Study- OSS 001/2016 - rif ENDO 30). The research was open to all specialists taking care of patients with diabetes in Italy.

The primary endpoint was glycemic control, evaluated by HbA1c levels, according to b/T.

Secondary endpoints were occurrence of major hypoglycemic episodes according to b/T; differences between patients with T1 and T2.

An ad hoc form was developed and used to record all medical findings. The form was emailed to all participating centers who then emailed or faxed it back to our data manager. Data were checked for accuracy.

The following data were required: age, gender, body weight and height, country of origin, type of diabetes and its duration, units of basal and total (basal plus prandial) daily insulin, type of basal insulin (Glargine, Detemir or Degludec), use and dosage of metformin, and number of major hypoglycemic episodes (<40 mg/dL or requiring caregivers intervention) in the last three months. Serum creatinine and HbA1c levels obtained within the previous two months were also required.

Each participating center recruited between 20 and 40 diabetic outpatients. Inclusion criteria were as follows: adult outpatients (≥20 and ≤80 years) with T1 or T2 diabetes mellitus, on basal-bolus insulin regimen (basal insulin, i.e. Glargine, Detemir or Degludec, plus at least two prandial insulin shots) for at least six months, usually assuming three daily meals, and capable of informed consent.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • adult outpatients (≥20 and ≤80 years);
  • T1 or T2 diabetes mellitus;
  • basal-bolus insulin regimen (basal insulin, i.e. Glargine, Detemir or Degludec, plus at least two prandial insulin shots) for at least six months;
  • assuming three daily meals;
  • capable of informed consent.

Exclusion criteria

  • pregnancy;
  • breast-feeding;
  • severe liver or renal failure (eGFR <30 mL/min/1.73 m2);
  • use of OADs (except for metformin);
  • hospitalization for any cause in the last six month;
  • glucocorticoid treatment in the last six month;
  • oncologic treatment in the last six month;
  • Ramadan in the last six months.

Treatment and study plan

Primary outcomes

  1. basal/total ratio

    Time frame: last six month

    To evaluate the basal/total ratio of daily insulin dose (b/T) in diabetic outpatients type 1 (T1) and type 2 (T2) on basal-bolus regimen

Secondary outcomes

  1. glycaemic control

    Time frame: last six month

    relationship between b/T ratio and HbA1c

  2. hypoglycemia

    Time frame: last six month

    relationship between b/T ratio and episodes of hypoglycemia

Sponsors and collaborators

Lead sponsor

Associazione Medici Endocrinologi

Other

Registry information

Official study title

Basal Study - Observational Multicentric Clinical Study: Basal Insulin And Compensation Glycemic In Diabetic Patients In Basal Bolus Outpatient.

Acronym: BASAL

Important dates

Study start
2016
Primary completion
2016
Study completion
2017
First posted
Apr 5, 2018
Registry last updated
Apr 5, 2018

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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