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Status unknownNCT01047722Aspirin-BVTUpdated Jul 21, 2015

In-Vivo Bleeding Volume Test for Platelet-Aspirin Interaction

A Phase 1 interventional study of Aspirin ingestion followed by doing a Bleeding Volume Test and Gatorade Placebo followed by Bleeding Volume Test. in Healthy, sponsored by Klein, Jeffrey A., M.D.. Status unknown at 2 sites in United States. Open to participants aged 18 Years to 89 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2015-07-21.

Sponsored by Klein, Jeffrey A., M.D. · Phase 1, Interventional, and Diagnostic

The sponsor has not verified this record recently (last verified Jul 2015), so the status shown — last known as Active, not recruiting — may be out of date.
Phase
Phase 1
Study type
Interventional
Enrollment
100
Allocation
Randomized
Ages
18 Years to 89 Years
Sex
All
01

Study summary

Purpose of the present research project is to study a new in-vivo test for abnormal platelet function and to study the effect of certain drugs on clinical bleeding. This is a randomized clinical trial of a new in-vivo test of platelet function known as the bleeding volume test(BVT)which relies on an on-line measurement system. This trial will assess the sensitivity and specificity of the new BVT by studying the effects of aspirin which is known to affect platelet function in-vivo. This is not a clinical trial of drugs. This is a clinical trial of a novel in-vivo on-line laboratory test.

The BVT measures the total volume of blood in the discrete blotches of blood on the blotter paper during the BT test and thus the BVT gleans valuable additional information from the bleeding time test (BTT)procedure. We hypothesize that the BV test will be a more accurate, specific and sensitive test for diagnosing platelet function abnormalities and for detecting a person's bleeding tendency compared to the BTT, and commercially available in-vitro platelet function tests.

Read the detailed description

Purpose of the present research project is to study a new in-vivo test for abnormal platelet function and to study the effect of certain drugs on clinical bleeding. This is a randomized clinical trial of a new in-vivo test of platelet function known as the bleeding volume (BV) test which relies on an on-line measurement system. This trial will assess the sensitivity and specificity of the new BV test by studying the effects of aspirin which is known to affect platelet function in-vivo. This is not a clinical trial of drugs. This is a clinical trial of a novel laboratory test. The BV test results will be compared to the results of two commercially available platelet function tests (the VerifyNow test and the PFA-100 test) which requires 10 ml of blood taken from a peripheral vein.

The bleeding volume test is an extension of the classic Ivy Bleeding Time Test (BTT). The BTT, an in-vivo test for an abnormal bleeding tendency, involves making a small standardized cut in the skin and measuring the duration of bleeding. We hypothesize that measuring both the volume of blood lost (BV) and the BT will to provide a more useful test. The BV test is expected to provide an improved in-vivo technique for 1) investigating the effects of drugs on platelet function and 2) diagnosing diseases of abnormal platelet function such as von Willebrand disease (vWD), 3) identifying patients who are aspirin-resistant in the sense that they do not benefit from the beneficial effects of aspirin in preventing thromboembolic disease (heart attack and stroke), 4) providing insight into the effects of antithrombotic drugs such as clopidogrel, lidocaine and statins (HMG-CoA reductase inhibitors). The BV test will provide an inexpensive diagnostic test and improve patient care.

02

Conditions studied

  • Healthy

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Keywords

  • platelet function test
  • platelets
  • in vivo test
  • aspirin
  • aspirin resistance
  • aspirin non-responsiveness
  • in-vivo
  • To assess the specificity and sensitivity of a novel in-vivo diagnostic test of platelet function
  • To use this test to define and assess "aspirin resistance"
03

In context

Hemorrhage

3,000 studies on the registry are indexed under Hemorrhage; 474 are open to participants now.

This study's planned enrollment of 100 is close to the median of 100 across 1,985 interventional studies indexed under Hemorrhage.

Browse Hemorrhage studies →

Lead sponsor

Klein, Jeffrey A., M.D. is the lead sponsor of 5 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 89 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Adult male and female
  • Ages 18 to 89 years old

Exclusion criteria

Exclusion Criteria:

  • Any history of HIV, Hepatitis C or presence of a blood-borne infectious disease
05

Study design

Phase
Phase 1
Primary purpose
Diagnostic
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
100 participants (estimated)

Study arms

  • Active comparator
    Patient drinks aspirin in Gatorade.

    Patient drinks Gatorade containing 325 mg aspirin. Bleeding Volume Test is done one hour later.

    Drug: Aspirin ingestion followed by doing a Bleeding Volume Test

  • Placebo comparator
    Gatorade Placebo

    Patient ingests Gatorade and one hour later a Bleeding Volume Test is performed

    Procedure: Gatorade Placebo followed by Bleeding Volume Test.

Interventions

  • DrugAspirin ingestion followed by doing a Bleeding Volume Test

    Patient drinks a glass of Gatorade containing 325 mg of aspirin, then one hour later a bleeding volume test is performed.

  • ProcedureGatorade Placebo followed by Bleeding Volume Test.

    Patient drinks a glass of Gatorade, then one hour later a bleeding volume test is performed.

06

What researchers measure

Primary outcomes

  1. Sensitivity, Specificity & ROC curve characteristics of the Bleeding Volume Test

    Time frame: one year

07

Study locations

2 sites
  • Private practice office
    Newport Beach, California 92660, United States
  • Capistrano Surgery Center
    San Juan Capistrano, California 92675, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 21, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01047722
Lead sponsor
Klein, Jeffrey A., M.D.
Responsible party
Jeffrey Alan Klein, MD (Principal Investigator, Klein, Jeffrey A., M.D.) — Principal investigator
First posted
Jan 13, 2010
Start date
Jan 2010
Primary completion
Oct 2015 (estimated)
Completion
Oct 2015 (estimated)
Last update
Jul 21, 2015

Study contacts

Jeffrey A Klein, MD
principal investigator · University of Californiia, Riverside

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jul 2015. You cannot join it, but the record below documents what was studied.

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