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Effect of Linagliptin on Diabetic patients with COVID-19

Evaluation of the effect of Linagliptin on the outcome of COVID-19 in hospitalized patient with Diabetes

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210812052156N1
Enrollment
70
Registered
2021-10-27
Start date
2021-10-12
Completion date
Unknown
Last updated
2021-11-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COVID-19. COVID-19, virus identified

Interventions

Intervention 1: Intervention group:After reviewing the criteria for entering the study and filling the consent form, patient will receive Tab Linagliptin 5mg(known as Melijent) once a day for 14 days

Sponsors

Gonabad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Consent to participate in research Diabetes Patients admitted to the ward with definite diagnosis of COVID-19 with PCR Disease severity of mild to moderate

Exclusion criteria

Exclusion criteria: Lack of interest to cooperate in research History of allergies to Linagliptin Taking interactive drugs at simultaneous use with linagliptin, according to FDA definition Adverse drug reactions occurrence

Design outcomes

Primary

MeasureTime frame
Peripheral capillary oxygen saturation. Timepoint: From the beginning of admission to the hospital and daily during admission. Method of measurement: Pulse oximeter.;Requirement of non-mechanical ventilation. Timepoint: From the beginning of admission to the hospital and discharge time. Method of measurement: Patient's file in hospital.;Requirement of mechanical ventilation. Timepoint: From the beginning of admission to the hospital and discharge time. Method of measurement: Patient's file in hospital.;Hospitalization duration. Timepoint: From the beginning of admission to the hospital and discharge time. Method of measurement: Patient's file in hospital.;Requirement of ICU. Timepoint: From the beginning of admission to the hospital and discharge time. Method of measurement: Patient's file in hospital.;Mortality. Timepoint: At the end of study. Method of measurement: Patient's file in hospital.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNahid Kheirabady

Gonabad University of Medical Sciences

Nahid.khey00@gmail.com+98 51 5723 6833

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026