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Terminated Phase 2 Interventional

Use of Activated Recombinant Human Factor VII in Cardiac Surgery

ClinicalTrials.gov ID: NCT00154427

Public ClinicalTrials.gov record NCT00154427. 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, 6:55 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

A Multi-centre, Randomised, Double-blind, Placebocontrolled, Dose Escalation Trial on Safety and Efficacy of Activated Recombinant Factor VII (rFVIIa/NovoSeven®) in the Treatment of Post-operative Bleeding in Patients Following Cardiac Surgery Requiring Cardiopulmonary Bypass

Study identification

NCT ID
NCT00154427
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novo Nordisk A/S
Industry
Enrollment
172 participants

Conditions and interventions

Interventions

  • activated recombinant human factor VII 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
Jul 31, 2004
Primary completion
Oct 31, 2007
Completion
Oct 31, 2007
Last update posted
Jan 11, 2017

2004 – 2007

United States locations

U.S. sites
18
U.S. states
15
U.S. cities
17
Facility City State ZIP Site status
Novo Nordisk Investigational Site Birmingham Alabama 35235
Novo Nordisk Investigational Site Tucson Arizona 85714
Novo Nordisk Investigational Site San Francisco California 94115
Novo Nordisk Investigational Site Denver Colorado 80262
Novo Nordisk Investigational Site Atlanta Georgia 30322
Novo Nordisk Investigational Site Baltimore Maryland 21287
Novo Nordisk Investigational Site Boston Massachusetts 02215
Novo Nordisk Investigational Site Camden New Jersey 08103
Novo Nordisk Investigational Site Syracuse New York 13210
Novo Nordisk Investigational Site The Bronx New York 10461
Novo Nordisk Investigational Site The Bronx New York 10467
Novo Nordisk Investigational Site Cleveland Ohio 44195
Novo Nordisk Investigational Site Oklahoma City Oklahoma 73117
Novo Nordisk Investigational Site Portland Oregon 97207
Novo Nordisk Investigational Site Danville Pennsylvania 17821
Novo Nordisk Investigational Site Houston Texas 77030
Novo Nordisk Investigational Site Norfolk Virginia 23507
Novo Nordisk Investigational Site Richmond Virginia 23298

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 45 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00154427, 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 Jan 11, 2017 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00154427 live on ClinicalTrials.gov.

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