Safety and Efficacy of I 0401 in the Treatment of Tibial Plateau Fractures Requiring Grafting
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ClinicalTrials.gov Identifier: NCT00409799 |
Recruitment Status :
Completed
First Posted : December 11, 2006
Last Update Posted : March 16, 2012
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Tibia Plateau Fractures | Drug: I-0401 (a new bone graft substitute) | Phase 2 |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 208 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Treatment |
Official Title: | A Phase 2 Randomized, Controlled, Open-label (Dose-blinded), Multi-center, Dose-finding Study of the Safety and Efficacy of I-0401 in the Treatment of Patients With Fractures of the Tibial Plateau Requiring Grafting. |
Study Start Date : | November 2006 |
Actual Primary Completion Date : | September 2011 |
Actual Study Completion Date : | September 2011 |

Arm | Intervention/treatment |
---|---|
Experimental: 1
Experimental - high dose
|
Drug: I-0401 (a new bone graft substitute)
1 time application |
Experimental: 2
Experimental - low dose
|
Drug: I-0401 (a new bone graft substitute)
1 time application |
Active Comparator: 3
Autograft
|
Drug: I-0401 (a new bone graft substitute)
1 time application |
- Radiographic Images [ Time Frame: All Follow-Up Visits ]
- Clinical assessments of the fracture site [ Time Frame: All Follow-Up Visits ]
- Blood parameters [ Time Frame: All Follow-Up Visits ]
- Vital signs [ Time Frame: At several Follow-Up visits ]
- Questionnaires of Life [ Time Frame: All Follow-Up Visits ]
- Pharmacoeconomic evaluation [ Time Frame: All Follow-Up Visits ]

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Radiological evidence of a tibial plateau fracture requiring grafting
- Females of child-bearing potential must be willing to undergo a pregnancy test (urine) prior to treatment start (at screening).
Exclusion Criteria:
- Concomitant ipsilateral fractures of the limb other than the fracture of the tibial plateau.
- Active or past history of malignant tumor.
- Evidence of systemic or localized infection at time of surgery.
- Pregnant or lactating females.

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00409799

Principal Investigator: | Peter Messmer, MD | Zurich University Hospital, Zurich, Switzerland |
Responsible Party: | Kuros Biosurgery AG |
ClinicalTrials.gov Identifier: | NCT00409799 |
Other Study ID Numbers: |
CS I-040101/02 |
First Posted: | December 11, 2006 Key Record Dates |
Last Update Posted: | March 16, 2012 |
Last Verified: | March 2012 |
Bone graft substitute Promotion of bone healing |
Fractures, Bone Tibial Plateau Fractures Wounds and Injuries Knee Fractures |
Tibial Fractures Knee Injuries Leg Injuries |