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A double-blind, randomized trial, including frequent patient-physician contacts and Ramadan-focused advice, assessing vildagliptin and gliclazide in patients with type 2 diabetes fasting during Ramadan: the STEADFAST study.
Hassanein, Mohamed; Abdallah, Khalifa; Schweizer, Anja.
Affiliation
  • Hassanein M; Betsi Cadwaladr University Health Board, Wales, United Kingdom.
  • Abdallah K; Clinical Research Center, Alexandria University Hospital, Alexandria, Egypt.
  • Schweizer A; Global Medical Affairs, Novartis Pharma AG, Basel, Switzerland.
Vasc Health Risk Manag ; 10: 319-26, 2014.
Article in En | MEDLINE | ID: mdl-24920915
BACKGROUND: Several observational studies were conducted with vildagliptin in patients with type 2 diabetes mellitus (T2DM) fasting during Ramadan, showing significantly lower incidences of hypoglycemia with vildagliptin versus sulfonylureas, including gliclazide. It was of interest to complement the existing real-life evidence with data from a randomized, double-blind, clinical trial. CLINICAL TRIALS IDENTIFIER: NCT01758380. METHODS: This multiregional, double-blind study randomized 557 patients with T2DM (mean glycated hemoglobin [HbA1c], 6.9%), previously treated with metformin and any sulfonylurea to receive either vildagliptin (50 mg twice daily) or gliclazide plus metformin. The study included four office visits (three pre-Ramadan) and multiple telephone contacts, as well as Ramadan-focused advice. Hypoglycemic events were assessed during Ramadan; HbA(1c) and weight were analyzed before and after Ramadan. RESULTS: The proportion of patients reporting confirmed (<3.9 mmol/L and/or severe) hypoglycemic events during Ramadan was 3.0% with vildagliptin and 7.0% with gliclazide (P=0.039; one-sided test), and this was 6.0% and 8.7%, respectively, for any hypoglycemic events (P=0.173). The adjusted mean change pre- to post-Ramadan in HbA(1c) was 0.05%±0.04% with vildagliptin and -0.03%±0.04% with gliclazide, from baselines of 6.84% and 6.79%, respectively (P=0.165). In both groups, the adjusted mean decrease in weight was -1.1±0.2 kg (P=0.987). Overall safety was similar between the treatments. CONCLUSION: In line with the results from previous observational studies, vildagliptin was shown in this interventional study to be an effective, safe, and well-tolerated treatment in patients with T2DM fasting during Ramadan, with a consistently low incidence of hypoglycemia across studies, accompanied by good glycemic and weight control. In contrast, gliclazide showed a lower incidence of hypoglycemia in the present interventional than the previous observational studies. This is suggested to be linked to the specific circumstances of this study, including frequent patient-physician contacts, Ramadan-focused advice, a recent switch in treatment, and very well-controlled patients, which is different from what is often seen in real life.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Office Visits / Pyrrolidines / Religion and Medicine / Telephone / Adamantane / Fasting / Diabetes Mellitus, Type 2 / Dipeptidyl-Peptidase IV Inhibitors / Gliclazide / Hypoglycemic Agents Type of study: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies Limits: Female / Humans / Male / Middle aged Country/Region as subject: Asia / Europa Language: En Journal: Vasc Health Risk Manag Journal subject: ANGIOLOGIA Year: 2014 Document type: Article Affiliation country: United kingdom Country of publication: New Zealand

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Office Visits / Pyrrolidines / Religion and Medicine / Telephone / Adamantane / Fasting / Diabetes Mellitus, Type 2 / Dipeptidyl-Peptidase IV Inhibitors / Gliclazide / Hypoglycemic Agents Type of study: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies Limits: Female / Humans / Male / Middle aged Country/Region as subject: Asia / Europa Language: En Journal: Vasc Health Risk Manag Journal subject: ANGIOLOGIA Year: 2014 Document type: Article Affiliation country: United kingdom Country of publication: New Zealand