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No Longer Available No phase listed Expanded access

Aprotinin US Special Access Protocol

ClinicalTrials.gov ID: NCT00611845

Public ClinicalTrials.gov record NCT00611845. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 12:58 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Aprotinin US Special Access Protocol: An Open Label, Non-Comparative Treatment Protocol for the Use of Aprotinin in Patients Undergoing Coronary Artery Bypass Graft Surgery Requiring Cardiopulmonary Bypass Who Are at Increased Risk of Blood Loss and Transfusion

Study identification

NCT ID
NCT00611845
Recruitment status
No Longer Available
Study type
Expanded access
Phase
Not listed
Lead sponsor
Bayer
Industry
Enrollment
Not listed

Conditions and interventions

Interventions

  • Aprotinin (Trasylol, BAYA0128) Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Not listed
Primary completion
Not listed
Completion
Not listed
Last update posted
Jun 22, 2014

United States locations

U.S. sites
17
U.S. states
11
U.S. cities
16
Facility City State ZIP Site status
Not listed Decatur Alabama 35601
Not listed Glendale California 91206
Not listed Pismo Beach California 93449
Not listed Santa Monica California 90404
Not listed Ventura California 93003
Not listed Fort Wayne Indiana 46804
Not listed Edgewood Kentucky 41017
Not listed New Brunswick New Jersey 08903
Not listed Asheville North Carolina 28805
Not listed Medford Oregon 97504
Not listed Portland Oregon 97210
Not listed Portland Oregon 97225
Not listed Philadelphia Pennsylvania 19107
Not listed Knoxville Tennessee 37917
Not listed Lynchburg Virginia 24501
Not listed Milwaukee Wisconsin 53215
Not listed Wausau Wisconsin 54401

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00611845, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 22, 2014 · Synced Jul 21, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00611845 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →