Tibial Delayed Healing Pivotal Clinical Trial
Public ClinicalTrials.gov record NCT01016067. 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
A Prospective, Randomized, Multicenter Pivotal Clinical Trial of the INFUSE/MASTERGRAFT™ Delayed Healing Device With Rigid Internal Fixation in the Treatment of Tibial Delayed Healing
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
Evaluate the INFUSE/MASTERGRAFT™ Delayed Healing Device as an alternative/replacement to autograft in the treatment of tibial delayed healing.
Study identification
- NCT ID
- NCT01016067
- Recruitment status
- Terminated
- Study type
- Interventional
- Phase
- Phase 3
- Enrollment
- 23 participants
Conditions and interventions
Conditions
Eligibility (public fields only)
- Age range
- 21 Years and older
- Sex
- All
- Healthy volunteers
- Accepts healthy volunteers
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Nov 2010 (Type not available)
- Primary completion
- Oct 2013 (Actual)
- Completion
- Dec 2013 (Actual)
- Last update posted
- Jan 21, 2015
2010 – 2013
United States locations
- U.S. sites
- 16
- U.S. states
- 12
- U.S. cities
- 16
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Denver Health | Denver | Colorado | 80204 | — |
| Shrock Orthopedic Research | Fort Lauderdale | Florida | 33316 | — |
| University of Florida College of Medicine | Jacksonville | Florida | 32209 | — |
| Orlando Health | Orlando | Florida | 32806 | — |
| Fort Wayne Orthopaedics | Fort Wayne | Indiana | 46804 | — |
| Methodist Hospital | Indianapolis | Indiana | 46202 | — |
| Sinai Hospital of Baltimore | Baltimore | Maryland | 21215 | — |
| William Beaumont Hospital | Royal Oak | Michigan | 48073 | — |
| University of Missouri | Columbia | Missouri | 65201 | — |
| St. Louis University Hospital | St Louis | Missouri | 63104 | — |
| Lutheran Medical Center | Brooklyn | New York | 11220 | — |
| Carolinas Medical Center | Charlotte | North Carolina | 28204 | — |
| Ohio Health Research Center | Columbus | Ohio | 43215 | — |
| University of Oklahoma | Oklahoma City | Oklahoma | 73104 | — |
| Geisinger Clinic | Danville | Pennsylvania | 17822 | — |
| Vanderbilt University Medical Center | Nashville | Tennessee | 37232 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT01016067, 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 21, 2015 · Synced Oct 21, 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 public registry record, listed eligibility criteria, and available contact information for NCT01016067 live on ClinicalTrials.gov.