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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Withdrawn Study Name: Study of Pamidronate for the Prevention of Heterotopic Ossification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Withdrawn Study Name: Naproxen for the Prevention of HO After Complex Elbow Trauma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:
  • Drug: Naproxen • Group 1
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:
  • Drug: Indomethacin and Pantoprazole
  • Drug:

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:
  • Drug: Palovarotene dose level 1

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:
  • Intervertebral Disk Degeneration
  • Intervertebral Disk Displacement
  • Device: Cervios ChronOs The AC
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