In-Vivo Bleeding Volume Test for Platelet-Aspirin Interaction

NCT ID: NCT01047722

Last Updated: 2015-07-21

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE1
• Total Enrollment: 100 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-01-31
• Study Completion Date: 2015-10-31

Brief 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.

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.

Conditions

Healthy

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: DIAGNOSTIC
• Blinding Strategy: DOUBLE

Study Groups

Patient drinks aspirin in Gatorade.

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

Group Type: ACTIVE_COMPARATOR

Aspirin ingestion followed by doing a Bleeding Volume Test

Intervention Type: DRUG

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

Gatorade Placebo

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

Group Type: PLACEBO_COMPARATOR

Gatorade Placebo followed by Bleeding Volume Test.

Intervention Type: PROCEDURE

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

Interventions

Aspirin 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.

Intervention Type: DRUG

Gatorade Placebo followed by Bleeding Volume Test.

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

Intervention Type: PROCEDURE

Eligibility Criteria

Inclusion Criteria

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

Exclusion Criteria

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

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 89 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Klein, Jeffrey A., M.D.

INDIV

Sponsor Role: lead

Responsible Party

Jeffrey Alan Klein, MD

Principal Investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Jeffrey A Klein, MD

Role: PRINCIPAL_INVESTIGATOR

University of Californiia, Riverside

Locations

Private practice office

Newport Beach, California, United States

Capistrano Surgery Center

San Juan Capistrano, California, United States

Countries

United States

Other Identifiers

3 BVT-ASA

Identifier Type: -

Identifier Source: org_study_id