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A Randomized Clinical Trial of Linagliptin vs. Standard of Care in Patients Hospitalized With Diabetes and COVID-19.
Abuhasira, Ran; Ayalon-Dangur, Irit; Zaslavsky, Neta; Koren, Ronit; Keller, Mally; Dicker, Dror; Grossman, Alon.
Affiliation
  • Abuhasira R; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Ayalon-Dangur I; Department of Internal Medicine B, Rabin Medical Center, Beilinson Campus, Petah Tikva, Israel.
  • Zaslavsky N; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Koren R; Department of Internal Medicine E, Rabin Medical Center, Beilinson Campus, Petah Tikva, Israel.
  • Keller M; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Dicker D; Department of Internal Medicine B, Rabin Medical Center, Beilinson Campus, Petah Tikva, Israel.
  • Grossman A; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Front Endocrinol (Lausanne) ; 12: 794382, 2021.
Article in En | MEDLINE | ID: mdl-35002970
ABSTRACT

Objective:

To assess the effect of linagliptin vs. standard therapy in improving clinical outcomes in patients hospitalized with diabetes and coronavirus disease 2019 (COVID-19). Materials and

Methods:

We did an open-label, prospective, multicenter, randomized clinical trial in 3 Israeli hospitals between October 1, 2020, and April 4, 2021. Eligible patients were adults with type 2 diabetes mellitus and a diagnosis of COVID-19. A total of 64 patients, 32 in each group, were randomized to receive linagliptin 5 mg PO daily throughout the hospitalization or standard of care therapy. The primary outcome was time to clinical improvement within 28 days after randomization, defined as a 2-point reduction on an ordinal scale ranging from 0 (discharged without disease) to 8 (death).

Results:

The mean age was 67 ± 14 years, and most patients were male (59.4%). Median time to clinical improvement was 7 days (interquartile range (IQR) 3.5-15) in the linagliptin group compared with 8 days (IQR 3.5-28) in the standard of care group (hazard ratio, 1.22; 95% CI, 0.70-2.15; p = 0.49). In-hospital mortality was 5 (15.6%) and 8 (25.0%) in the linagliptin and standard of care groups, respectively (odds ratio, 0.56; 95% CI, 0.16-1.93). The trial was prematurely terminated due to the control of the COVID-19 outbreak in Israel.

Conclusions:

In this randomized clinical trial of hospitalized adult patients with diabetes and COVID-19 who received linagliptin, there was no difference in the time to clinical improvement compared with the standard of care. Clinical Trial Registration ClinicalTrials.gov, identifier NCT04371978.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Diabetes Mellitus, Type 2 / Dipeptidyl-Peptidase IV Inhibitors / Standard of Care / Linagliptin / SARS-CoV-2 / COVID-19 / Hospitalization Type of study: Clinical_trials / Observational_studies / Risk_factors_studies Limits: Aged / Female / Humans / Male Country/Region as subject: Asia Language: En Journal: Front Endocrinol (Lausanne) Year: 2021 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Diabetes Mellitus, Type 2 / Dipeptidyl-Peptidase IV Inhibitors / Standard of Care / Linagliptin / SARS-CoV-2 / COVID-19 / Hospitalization Type of study: Clinical_trials / Observational_studies / Risk_factors_studies Limits: Aged / Female / Humans / Male Country/Region as subject: Asia Language: En Journal: Front Endocrinol (Lausanne) Year: 2021 Document type: Article Affiliation country: