Menu
Not yet recruiting NCT07084272

PRP Yield and Platelet Distribution With EDTA

Observational PRP

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: PRP. Basic parameters: 18 years — 75 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

A Comparison Study of ACD-A and EDTA Anticoagulation of Platelet-rich Plasma: Yields and Platelet Distribution

Overview

We will test and compare the platelet distribution after centrifugation and the platelet yield of ACD-A and EDTA anticoagulated blood

Primary outcome measures

  • Platelet yield [Time frame: 5 months]
  • Platelet yield [Time frame: 5 months]

Eligibility criteria

Inclusion criteria

\-

Exclusion criteria

  • blood dyscrasias

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07084272 · PRPEDTA

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗