Clinical Trials Logo

Pseudoarthrosis clinical trials

View clinical trials related to Pseudoarthrosis.

Filter by:
  • None
  • Page 1

NCT ID: NCT03382665 Terminated - Clinical trials for Rheumatoid Arthritis

Post-market Surveillance Study With the HYPERION Hip Endoprosthesis System in Defect Reconstruction

Start date: January 2010
Phase:
Study type: Observational

The study is a multi-center, prospective, non-controlled, consecutive cohort post market surveillance study. The objective of this study is to obtain survival and clinical outcome data on the Hyperion® system in primary and revision total hip arthroplasty.

NCT ID: NCT02520089 Completed - Pseudoarthrosis Clinical Trials

Humeral Shaft Pseudoarthrosis Treated With Bone Autograft Versus Platelet Rich Plasma

Start date: November 2014
Phase: N/A
Study type: Interventional

Patients with humeral shaft pseudoarthrosis is going to be treated with a standard protocol with a locking compression plate and bone autograft, and other group of patients treated with platelet rich plasma. Posteriorly all the patients it will evaluated radiographically and with functional scales for a period of one year.

NCT ID: NCT02483364 Completed - Pseudoarthrosis Clinical Trials

A Clinical Trial to Assess the Effect of HC-SVT-1001 and HC-SVT-1002 in the Surgical Treatment of Atrophic Pseudarthrosis of Long Bones (Bonecure)

Bonecure
Start date: November 10, 2015
Phase: Phase 2
Study type: Interventional

The purpose os this study is to evaluate the safety and effectiveness of HC-SVT-1001 and HC-SVT-1002 in the surgical treatment of atrophic nonunion in long bones.

NCT ID: NCT01972256 Completed - Spinal Stenosis Clinical Trials

A Study Comparing Fusion Rates of Two Lumbar Fusion Procedures

Start date: April 2013
Phase: N/A
Study type: Observational

The purpose of this study is to demonstrate the relative efficacy of two lumbar fusion procedures: transacral lumbar interbody fusion when used in conjunction with unilateral or bilateral posterior pedicle screw fixation as an adjunct to fusion, in comparison to transforaminal lumbar interbody fusion (TLIF) when used in conjunction with unilateral or bilateral supplemental screw fixation as an adjunct to fusion. Subject candidates are those who had previously required and received fusion at L4-L5-S1 where these were the only lumbar levels treated for pseudoarthrosis, spinal stenosis, spondylolisthesis, or degenerative disc disease (DDD).

NCT ID: NCT01813188 Completed - Pseudoarthrosis Clinical Trials

Clinical Trial Based on the Use of Mononuclear Cells From Autologous Bone Marrow in Patients With Pseudoarthrosis

Start date: April 2011
Phase: Phase 2
Study type: Interventional

The purpose of this clinical trial is to check the non-inferiority and lower morbidity of the use of bone marrow mononuclear cells seeded onto a porous matrix of calcium phosphate, for the consolidation of tibial bone defects (pseudoarthrosis), compared with autologous bone graft.

NCT ID: NCT01528072 Terminated - Clinical trials for Degenerative Spondylolisthesis

Dynesys Spinal System Post Market 522 Study

Start date: March 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the safety and fusion rates following posterior lateral fusion with the Dynesys Spinal System used as an adjunct to fusion and compare to literature control.