BIOHELIX-I Bare Metal Stent Study
Public ClinicalTrials.gov record NCT01612767. 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.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
The Treatment of Coronary Artery Lesions Using the PRO-Kinetic Energy Cobalt-Chromium, Bare-Metal Stent
Study identification
- NCT ID
- NCT01612767
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Phase 2, Phase 3
- Lead sponsor
- Biotronik, Inc.
- Industry
- Enrollment
- 329 participants
Conditions and interventions
Conditions
Interventions
- PRO-Kinetic Energy Stent Device
Device
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
- Oct 31, 2012
- Primary completion
- Aug 31, 2015
- Completion
- Oct 31, 2017
- Last update posted
- Sep 27, 2018
2012 – 2017
United States locations
- U.S. sites
- 28
- U.S. states
- 19
- U.S. cities
- 27
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Not listed | Phoenix | Arizona | 85020 | — |
| Not listed | Concord | California | 94520 | — |
| Not listed | Mission Viejo | California | 92691 | — |
| Not listed | Danbury | Connecticut | 06810 | — |
| Not listed | New Haven | Connecticut | 06511 | — |
| Not listed | Washington D.C. | District of Columbia | 20010 | — |
| Not listed | Gainesville | Georgia | 30501 | — |
| Not listed | Indianapolis | Indiana | 46290 | — |
| Not listed | Iowa City | Iowa | 52242 | — |
| Not listed | Lafayette | Louisiana | 70506 | — |
| Not listed | Lewiston | Maine | 04240 | — |
| Not listed | Takoma Park | Maryland | 20912 | — |
| Not listed | Kansas City | Missouri | 64132 | — |
| Not listed | Springfield | Missouri | 65804 | — |
| Not listed | Newark | New Jersey | 07102 | — |
| Not listed | New York | New York | 10029 | — |
| Not listed | New York | New York | 10065 | — |
| Not listed | Poughkeepsie | New York | 12601 | — |
| Not listed | Gastonia | North Carolina | 28054 | — |
| Not listed | High Point | North Carolina | 27262 | — |
| Not listed | Columbus | Ohio | 43210 | — |
| Not listed | Portland | Oregon | 97239 | — |
| Not listed | Anderson | South Carolina | 29621 | — |
| Not listed | Greenville | South Carolina | 29605 | — |
| Not listed | Amarillo | Texas | 79106 | — |
| Not listed | McKinney | Texas | 75069 | — |
| Not listed | Tyler | Texas | 75701 | — |
| Not listed | Mechanicsville | Virginia | 23116 | — |
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 7 non-U.S. sites.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT01612767, 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 Sep 27, 2018 · Synced Jul 24, 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 NCT01612767 live on ClinicalTrials.gov.