Search for Clinical Trial Results

Ossification, Heterotopic - 18 Studies Found
Status | Study |
Recruiting |
Study Name: Celecoxib for Primary Prophylaxis of Combat-Related Heterotopic Ossification Condition: Ossification, Heterotopic Date: 2012-06-27 Interventions: Drug: Celecoxib 200 mg Q 12 hours orally Other Name: |
Completed |
Study Name: Prevention of Heterotopic Ossification With Arcoxia After Total Hip Replacement Condition: Ossification, Heterotopic Date: 2009-11-27 Interventions: Drug: Etoricoxib (Arcoxia) Oral intake of 90 mg Etoricoxib (Arcoxia) during 7-days |
Withdrawn |
Study Name: Study of Pamidronate for the Prevention of Heterotopic Ossification Condition: Heterotopic Ossification Date: 2005-12-05 Interventions: Drug: Pamidronate (AREDIA) Pamidronate (AREDIA) vs radiation |
Withdrawn |
Study Name: Naproxen for the Prevention of HO After Complex Elbow Trauma Condition: Heterotopic Ossification Date: 2007-12-14 Interventions: Drug: Naproxen 500 mg Naproxen twice a day for two weeks |
Active, not recruiting |
Study Name: Influence of Naproxen on Heterotropic Bone Formation Following Hip Arthroscopy Condition: Heterotopic Ossification Date: 2012-01-12 Interventions:
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Recruiting |
Study Name: Indomethacin Prophylaxis for Heterotopic Ossification After Surgical Treatment of Elbow Trauma Condition: Elbow Trauma Requiring Operative Management Date: 2012-11-19 Interventions:
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Completed |
Study Name: Radiation Therapy for Heterotopic Ossification Prophylaxis Acutely After Elbow Trauma Condition: Elbow Fracture Date: 2009-10-07 Interventions: Radiation: Radiation Therapy (XRT) The dose will be 700 cGy in a single fraction, using AP-PA fields cal |
Active, not recruiting |
Study Name: An Open-Label Extension Study of Palovarotene to Prevent Heterotopic Ossification in FOP Subjects in France Condition: Fibrodysplasia Ossificans Progressiva Date: 2016-11-23 Interventions:
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Recruiting |
Study Name: ESWT as a Treatment for Chronic NHO in TBI Patients Condition: TBI Traumatic Brain Injury Date: 2014-12-16 Interventions: Device: ESWT - Extracorporeal Shockwave Therapy Patients w |
Completed |
Study Name: Evaluation of Fusion Rate of Anterior Cervical Discectomy and Fusion (ACDF) Using Cervios ChronOs™ and Bonion™ Condition:
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