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Completed Phase 4 Interventional Results available

PRET: Patients Prone to Recurrence After Endovascular Treatment

ClinicalTrials.gov ID: NCT00626912

Public ClinicalTrials.gov record NCT00626912. 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 Sep 5, 2026, 11:45 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

PRET: Patients Prone to Recurrence After Endovascular Treatment. A Randomized Trial Comparing Platinum and Hydrogel-coated Coils

Brief summary

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

The PRET study aims at comparing two types of coils used in the endovascular treatment of intracranial aneurysms. The first type made of platinum has been used for more than 15 years. The other, referred to as hydrocoil, containing in addition to platinum a polymer layer that expands when in contact with blood, has been in use since 2002. The hypothesis of the PRET study is that the newer hydrocoil will be more effective and yet as safe as the older platinum coil.

Study identification

NCT ID
NCT00626912
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Enrollment
447 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 31, 2007
Primary completion
Sep 30, 2015
Completion
Nov 30, 2015
Last update posted
Mar 25, 2019

2007 – 2015

United States locations

U.S. sites
18
U.S. states
14
U.S. cities
18
Facility City State ZIP Site status
Shands - University of Florida Hospital Gainesville Florida
Borgess Medical Center Kalamazoo Michigan
Mayo Clinic Rochester Rochester Minnesota
University of Mississipi Health Care Jackson Mississippi 39216
Saint Francis Medical Center Cape Girardeau Missouri
Washington University in St Louis St Louis Missouri
University of Buffalo (SUNY) Buffalo New York
Stony Brook University Medical Center (SUNY) Stony Brook New York
SUNY Upstate Medical University Syracuse New York
University of Cincinnati Medical Center Cincinnati Ohio
Cleveland Clinic Cleveland Ohio
University of Oklahoma Health Sciences Center Oklahoma City Oklahoma
Oregon Health and Science University Portland Oregon
Medical University of South Carolina Charleston South Carolina
The Methodist Hospital Houston Texas
University of Virginia Health System Charlottesville Virginia
West Virginia University Hospital Morgantown West Virginia
University of Wisconsin Hospital and Clinics Madison Wisconsin

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 14 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00626912, 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 Mar 25, 2019 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00626912 live on ClinicalTrials.gov.

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