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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT04626089
Other study ID # SIL-30000-II(1)
Secondary ID
Status Withdrawn
Phase Phase 2
First received
Last updated
Start date February 2021
Est. completion date February 2021

Study information

Verified date November 2020
Source Laboratorios Silanes S.A. de C.V.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the efficacy and safety of metformin glycinate at dose of 620 mg twice per day plus standard treatment comparing to standard treatment alone (we will use placebo) of patients who have metabolic syndrome or type 2 diabetes, which have severe acute respiratory syndrome secondary to SARS-CoV-2.


Description:

After being informed about the study and potential risks, all patients will give written informed consent and undergo a 1 day screening period to determine the eligibility for study entry. At day 0, patients who meet the eligibility requirements will be randomized in a double blind (participant and investigator) in a 1:1 ratio to metformin glycinate (620 mg, taken orally twice daily) plus standard treatment or placebo (taken orally,twice daily) plus standard treatment, both will be for 14 days.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date February 2021
Est. primary completion date February 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. = 18 years old 2. Ability to understand and the willingness to sign a written informed consent document before any study procedure 3. Metabolic syndrome or type 2 diabetes 4. Coronavirus infection, severe acute respiratory syndrome SARS-CoV- 2 confirmed by the Polymerase Chain Reaction test (PCR) = 4 days before of the randomization. 5. Hospitalized patient. 6. Radiographic evidence of pulmonary infiltrates Exclusion Criteria: 1. Participation in any other clinical trial of an experimental treatment for COVID-19 2. Evidence of multi-organ failure 3. Require mechanical ventilation before randomization 4. Pregnant patients

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
metformin glycinate
Participants randomized to metformin glycinate wil take 620 mg bid (PO) plus standard treatment for 14 days
Placebo oral tablet
Participants randomized to placebo will take a tablet bid (PO) plus standard treatment for 14 days

Locations

Country Name City State
Mexico Hospital Juárez de México, OPD Mexico City

Sponsors (1)

Lead Sponsor Collaborator
Laboratorios Silanes S.A. de C.V.

Country where clinical trial is conducted

Mexico, 

References & Publications (49)

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* Note: There are 49 references in allClick here to view all references

Outcome

Type Measure Description Time frame Safety issue
Primary Viral Load Assess differences in SARS-CoV-2 viral load between participants that receive placebo vs metformin glycinate Day 0 to Day 8 or patient discharge day
Secondary Days of supplementary oxygen if apply Assess length of supplementary oxygen Day 0 to day 28 or patient discharge day
Secondary Days of supplementary mechanical ventilation if apply Assess length of mechanical ventilation Day 0 to day 28 or patient discharge day
Secondary Days of Hospitalization Assess length of hospitalization Day 0 to day 28 or patients discharge day
Secondary Normalization of fever Assess the difference in the Proportion of participants with normalization of fever between participants that receive placebo vs the patients with metformin glycinate Day 0 to day 28 or patient discharge day
Secondary Normalization of oxigen saturation Assess the difference in the Proportion of participants with normalization of oxygen saturation between participants that receive placebo vs the patients with metformin glycinate Day 0 to day 28 or patient discharge day
Secondary Number of deaths Assess the difference in the number of deaths between participants who received placebo versus the patients with metformin glycinate Day 0 to day 28 or patient discharge day
Secondary Change in Serum creatinine levels Evaluate if the level increase or decrease in serum creatinine compared to baseline. units: mg/dl Day 0 to day 28 or patients discharge day
Secondary Change in serum Troponin I Evaluate if the level increase or decrease in serum Creatine kinase-MB compared to baseline. Units: UI/l Day 0 to day 28 or patients discharge day
Secondary Change in serum aspartate aminotransferase levels Evaluate if the level increase or decrease in serum aspartate aminotransferase compared to baseline. units: IU/l Day 0 to day 28 or patients discharge day
Secondary Change in serum Creatine kinase-MB levels Evaluate if the level increase or decrease in serum Creatine kinase-MB compared to baseline. Units: UI/l Day 0 to day 28 or patients discharge day
Secondary Incidence of adverse event Assess by incidence of grade 3, grade 4 and Serious adverse events Day 0 to day 28 or patients discharge day
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