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NCT04212819

Before and After Erythrocyte Suspension Transfusion

Completed NA Last updated 2 January 2020
What this trial tests

NA trial testing Before Erythrocyte Suspension (ES) in Anemia in 50 participants. Completed in 31 December 2015.

Timeline
1 January 2014
Primary endpoint
1 April 2015
31 December 2015

Quick facts

Lead sponsorAfyonkarahisar Health Sciences University
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposesupportive care
Enrollment50
Start date1 January 2014
Primary completion1 April 2015
Estimated completion31 December 2015

Drugs / interventions tested

Conditions studied

Sponsor

Afyonkarahisar Health Sciences University

Who can join

Adults 18 to 80, any sex, with Anemia or Oxidative Stress. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Hypoperfusion, hypoxia and ischemia occurs in circulation as a result of anemia. All of these situations lead to oxidative stress and endothelial dysfunction in the organism. In this study, the investigators aimed to investigate the oxidant-antioxidant balance and asymmetric dimethylarginine (ADMA) levels in patients that have symptomatic anemia in need of erythrocyte suspension (ES) transfusion. To the best of the investigators knowledge, there have been few studies in the literature on anemia and total oxidant, total antioxidant and ADMA levels. We aimed to observe changes in oxidative - antioxidant ADMA levels before and after ES transfusion.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Anemia

Currently open trials in the same condition.

Other Afyonkarahisar Health Sciences University trials

Trials by the same sponsor.

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Data sources for this page

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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing