Blood tube study checks if device boosts healing cells
NCT ID NCT07041918
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested a medical device called VACUSERA PRP Tube, which is used to make platelet-rich plasma (PRP) from a person's own blood. PRP is sometimes used to help healing. The study involved 194 healthy volunteers and measured how well the tube increased the concentration of platelets compared to whole blood. No treatment was given; it was only a performance check of the device.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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194 people
The number who actually took part.
- Started
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May 2025
- Finished
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Jul 2025
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Male or female volunteers between the ages of 18 and 60, as defined in the target population during screening,
- Ages
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18 to 60 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
INCLUSION CRITERIA Male or female volunteers between the ages of 18 and 60, as defined in the target population during screening, Body Mass Index (BMI) between 18 and 32 during screening, No pregnancy or risk of pregnancy for women, Willing to participate and provide written informed consent and comply with the study restrictions, Must not have participated in any clinical trial within 2 months prior to the start of the study, Must be able to communicate with the researcher or authorized personnel. EXCLUSION CRITERIA Platelet dysfunction syndrome, Critical thrombocytopenia, Hemodynamic instability, Septicemia, Local infection at the site of the procedure, Autoimmune diseases, History of chronic infections, Chronic liver pathology, Patients receiving anticoagulant/antiplatelet therapy, Use of NSAIDs (except for paracetamol) in the last 7-10 days, History of alcohol and/or drug addiction, Corticosteroid use, Fever or illness in the past week, Cancer (especially blood and bone cancers), Hemoglobin (HGB) levels below 10 g/dl or above 16.5 g/dl in men and 16 g/dl in women, Platelet count below 105/μl, Those under immunosuppressive therapy, Any condition or disease detected during the medical interview/physical examination that, in the opinion of the researcher or designated personnel, would make the volunteer unsuitable for the study, put them at unnecessary risk, or interfere with the volunteer's ability to complete the study, Clinically significant deviation from normal findings in the physical examination, including vital signs, Patients planning pregnancy or not using contraception, Patients using hormonal contraceptive methods to prevent pregnancy, Breastfeeding women, Poor venous access for blood sampling, Plasma or blood donation within the last 2 months, It is recommended to select patients who do not use tobacco products during the study, as it is considered that it may affect the product's performance.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Medical Point Hastanesi Klinik Araştırmalar Merkezi
Izmir, Karşıyaka, 35575, Turkey (Türkiye)
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