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Completed Phase 2 Interventional Results available

Intracerebral Hemorrhage Deferoxamine Trial - iDEF Ttrial

ClinicalTrials.gov ID: NCT02175225

Public ClinicalTrials.gov record NCT02175225. 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 24, 2026, 9:27 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

Study of Deferoxamine Mesylate in Intracerebral Hemorrhage

Study identification

NCT ID
NCT02175225
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Beth Israel Deaconess Medical Center
Other
Enrollment
294 participants

Conditions and interventions

Interventions

  • Deferoxamine Mesylate Drug
  • Placebo (for Deferoxamine Mesylate) Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 80 Years
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
Sep 30, 2014
Primary completion
Feb 9, 2018
Completion
May 29, 2018
Last update posted
May 29, 2019

2014 – 2018

United States locations

U.S. sites
25
U.S. states
17
U.S. cities
21
Facility City State ZIP Site status
St. Joseph's Hospital / Barrow Neurological Institute Phoenix Arizona
Stanford University Medical Center Palo Alto California
San Francisco General Hospital San Francisco California
Yale New Haven Hospital New Haven Connecticut
University of Florida Jacksonville Florida
Loyola University Medical Center Chicago Illinois
RUSH University Medical Center Chicago Illinois
University of Iowa Medical Center Iowa City Iowa
Johns Hopkins Hospital Baltimore Maryland
Beth Israel Deaconess Medical Center Boston Massachusetts
UMass Memorial Medical Center Worcester Massachusetts
Henry Ford Hospital Detroit Michigan
Columbia University New York New York
Mount Sinai Hospital New York New York
NYU Langone Medical Center New York New York
Weill Medical College of Cornell University New York New York
University of North Carolina Medical Center Chapel Hill North Carolina
Duke University Medical Center Durham North Carolina
University Hospital Case Medical Center Cleveland Ohio
The Ohio State University Medical Center Columbus Ohio
Oregon Health & Science University Medical Center Portland Oregon
University of Pennsylvania Medical Center Philadelphia Pennsylvania
Rhode Island Hospital Providence Rhode Island
Medical University of South Carolina Charleston South Carolina
University of Texas Health Sciences Center Houston Texas

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 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02175225, 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 May 29, 2019 · Synced Jul 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02175225 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →