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Clinical Trials/NCT04375124
NCT04375124
Completed
Not Applicable

Evaluation of the Possible Role of Angiotensin Peptide (1-7) on Treatment of COVID-19

Kanuni Sultan Suleyman Training and Research Hospital1 site in 1 country9 target enrollmentApril 25, 2020
ConditionsCOVID-19

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
COVID-19
Sponsor
Kanuni Sultan Suleyman Training and Research Hospital
Enrollment
9
Locations
1
Primary Endpoint
mortality
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

Novel Coronavirus is reported to cause COVID-19, recently. It's known that this virus uses ACE (angiotensin converting enzyme) 2 receptors to enter human cells and also blocks the activity of ACE 2. Upon these data the investigators hypothesize that, mortal hyper-inflammation state which is shown in COVID-19 cases, can be a result of angiotensin peptide (1-7) deficiency. Therefore, the aim of this study is to evaluate the possible effect of angiotensin peptide (1-7) supplementation on treatment of COVID-19 cases.

Detailed Description

Novel Coronavirus is reported to cause COVID-19, recently. It's known that this virus uses ACE (angiotensin converting enzyme) 2 receptors to enter human cells and also blocks the activity of ACE 2. Upon these data the investigators hypothesize that, mortal hyper-inflammation state which is shown in COVID-19 cases, can be a result of angiotensin peptide (1-7) deficiency. Therefore, the aim of this study is to evaluate the possible effect of plasma derived angiotensin peptide (1-7) supplementation on treatment of COVID-19 cases.

Registry
clinicaltrials.gov
Start Date
April 25, 2020
End Date
September 30, 2020
Last Updated
4 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Hasan Onal

Professor

Kanuni Sultan Suleyman Training and Research Hospital

Eligibility Criteria

Inclusion Criteria

  • accepted to participate with an informed consent
  • proven positive COVID-19

Exclusion Criteria

  • declined to participate
  • genetic/chromosomal abnormalities
  • any kind of history of previous adverse events with transfusion
  • diagnosis of immune deficiency

Outcomes

Primary Outcomes

mortality

Time Frame: 4 months

mortality rates in two groups will be compared

Study Sites (1)

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