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Completed Phase 3 Interventional

Recombinant Factor VIIa in Acute Intracerebral Haemorrhage

ClinicalTrials.gov ID: NCT00127283

Public ClinicalTrials.gov record NCT00127283. 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 Oct 22, 2026, 5:38 AM EDT

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

Official title

Randomised, Double-Blind, Placebo Controlled, Multi-Centre, Parallel Groups Confirmatory Efficacy and Safety Trial of Activated Recombinant Factor VII (NovoSeven®/Niastase®) in Acute Intracerebral Haemorrhage

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This trial is conducted in Asia, Europe, Middle East, North America, Oceania, and South America. The purpose of this study is to evaluate the treatment of Recombinant Factor VIIa (eptacog alfa (activated)) in patients with acute intracerebral bleeding. It is expected that more patients will recover without severe permanent disability after acute treatment with Recombinant Factor VIIa by reducing further intracerebral bleeding.

Study identification

NCT ID
NCT00127283
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novo Nordisk A/S
Industry
Enrollment
829 participants

Conditions and interventions

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
May 2005 (Type not available)
Primary completion
Jan 2007 (Actual)
Completion
Jan 2007 (Actual)
Last update posted
Jan 12, 2017

2005 – 2007

United States locations

U.S. sites
77
U.S. states
35
U.S. cities
68
Facility City State ZIP Site status
Novo Nordisk Investigational Site Birmingham Alabama 35209 —
Novo Nordisk Investigational Site Mobile Alabama 36617 —
Novo Nordisk Investigational Site Phoenix Arizona 85013 —
Novo Nordisk Investigational Site Fort Smith Arkansas 72901 —
Novo Nordisk Investigational Site Los Angeles California 90024 —
Novo Nordisk Investigational Site Oceanside California 92056 —
Novo Nordisk Investigational Site Orange California 92868-4280 —
Novo Nordisk Investigational Site Sacramento California 95816 —
Novo Nordisk Investigational Site San Diego California 92103 —
Novo Nordisk Investigational Site San Francisco California 94110-3594 —
Novo Nordisk Investigational Site San Francisco California 94143-0780 —
Novo Nordisk Investigational Site Stanford California 94305 —
Novo Nordisk Investigational Site Denver Colorado 80204 —
Novo Nordisk Investigational Site Denver Colorado 80262 —
Novo Nordisk Investigational Site Englewood Colorado 80113 —
Novo Nordisk Investigational Site Hartford Connecticut 06102 —
Novo Nordisk Investigational Site Washington D.C. District of Columbia 20010 —
Novo Nordisk Investigational Site Jacksonville Florida 32209 —
Novo Nordisk Investigational Site Melbourne Florida 32901 —
Novo Nordisk Investigational Site Tallahassee Florida 32308 —
Novo Nordisk Investigational Site Tampa Florida 33606 —
Novo Nordisk Investigational Site Atlanta Georgia 30320 —
Novo Nordisk Investigational Site Augusta Georgia 30912-3260 —
Novo Nordisk Investigational Site Decatur Georgia 33033 —
Novo Nordisk Investigational Site Honolulu Hawaii 96813 —
Novo Nordisk Investigational Site Chicago Illinois 60611 —
Novo Nordisk Investigational Site Chicago Illinois 60612 —
Novo Nordisk Investigational Site Maywood Illinois 60153 —
Novo Nordisk Investigational Site Peoria Illinois 61637 —
Novo Nordisk Investigational Site Fort Wayne Indiana 46805 —
Novo Nordisk Investigational Site Indianapolis Indiana 46260 —
Novo Nordisk Investigational Site Iowa City Iowa 52242 —
Novo Nordisk Investigational Site Lexington Kentucky 40536 —
Novo Nordisk Investigational Site Louisville Kentucky 40202 —
Novo Nordisk Investigational Site Baltimore Maryland 21287 —
Novo Nordisk Investigational Site Boston Massachusetts 02118 —
Novo Nordisk Investigational Site Boston Massachusetts 02144 —
Novo Nordisk Investigational Site Boston Massachusetts 02215 —
Novo Nordisk Investigational Site Detroit Michigan 48201 —
Novo Nordisk Investigational Site Golden Valley Minnesota 55422 —
Novo Nordisk Investigational Site Blackwater Mississippi 39216 —
Novo Nordisk Investigational Site Kansas City Missouri 64111 —
Novo Nordisk Investigational Site St Louis Missouri 63110-1010 —
Novo Nordisk Investigational Site St Louis Missouri 63110 —
Novo Nordisk Investigational Site Las Vegas Nevada 89109 —
Novo Nordisk Investigational Site Lebanon New Hampshire 03756-0001 —
Novo Nordisk Investigational Site Cherry Hill New Jersey 08034 —
Novo Nordisk Investigational Site Hackensack New Jersey 07465 —
Novo Nordisk Investigational Site Ridgewood New Jersey 07450 —
Novo Nordisk Investigational Site Buffalo New York 14215 —
Novo Nordisk Investigational Site New York New York 10032 —
Novo Nordisk Investigational Site Stony Brook New York 11794-8121 —
Novo Nordisk Investigational Site Chapel Hill North Carolina 27599-7025 —
Novo Nordisk Investigational Site Charlotte North Carolina 28232-2861 —
Novo Nordisk Investigational Site Durham North Carolina 27705 —
Novo Nordisk Investigational Site Winston-Salem North Carolina 27103 —
Novo Nordisk Investigational Site Cincinnati Ohio 45267 —
Novo Nordisk Investigational Site Cleveland Ohio 44195 —
Novo Nordisk Investigational Site Portland Oregon 97225 —
Novo Nordisk Investigational Site Portland Oregon 97239 —
Novo Nordisk Investigational Site Allentown Pennsylvania 18103-6208 —
Novo Nordisk Investigational Site Philadelphia Pennsylvania 19104 —
Novo Nordisk Investigational Site Philadelphia Pennsylvania 19107 —
Novo Nordisk Investigational Site Pittsburgh Pennsylvania 15212-4746 —
Novo Nordisk Investigational Site Pittsburgh Pennsylvania 15213-2546 —
Novo Nordisk Investigational Site Charleston South Carolina 29425 —
Novo Nordisk Investigational Site Chattanooga Tennessee 37403 —
Novo Nordisk Investigational Site Hashville Tennessee 37232 —
Novo Nordisk Investigational Site Memphis Tennessee 38163 —
Novo Nordisk Investigational Site Nashville Tennessee 37205 —
Novo Nordisk Investigational Site Dallas Texas 75390-8897 —
Novo Nordisk Investigational Site Houston Texas 77030 —
Novo Nordisk Investigational Site San Antonio Texas 78229 —
Novo Nordisk Investigational Site Burlington Vermont 05401 —
Novo Nordisk Investigational Site Charlottesville Virginia 22908 —
Novo Nordisk Investigational Site Seattle Washington 98102 —
Novo Nordisk Investigational Site Madison Wisconsin 53792-3236 —

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 90 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00127283, 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 12, 2017 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00127283 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →