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Osteonecrosis of Femoral Head clinical trials

View clinical trials related to Osteonecrosis of Femoral Head.

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NCT ID: NCT04594564 Recruiting - Osteoarthritis, Hip Clinical Trials

Squeaking in Ceramic-on-Ceramic Total Hip Arthroplasty Using Delta TT Cup

Start date: October 1, 2020
Phase:
Study type: Observational

This study will evaluate clinical outcome on patients who undergo ceramic on ceramic (CoC) bearing total hip arthroplasty (THA) using Delta TT cup.

NCT ID: NCT04266236 Recruiting - Hip Fractures Clinical Trials

LPB Combined With QLB Using Single-needle Technique (LPQLB-SNT) for Hip Arthroplasty

LPQLB-SNT
Start date: July 9, 2020
Phase: N/A
Study type: Interventional

Total hip arthroplasty (THA) is one of the most successful orthopedic procedures to effectively relieve pain and restore function in patients with hip osteoarthritis, osteonecrosis of femoral head and hip fracture.The Lumbar Plexus Block (LPB) is currently used as the standard regional anesthesia technique to provide postoperative pain management after THA. The lumbar plexus (LP) originates from T12 to L5. In general, multiple-needle nerve blockade procedure is needed to block different branches of LP. Therefore, we need more time to finish the regional anethesia procedure and it's not easy for an inexperienced anesthesiologist to master the technique absolutely. In addition, multiple injections will increase the discomfort of the patients. We aim to investigate the effects of lumbar plexus combined with quadratus lumborum block using single-needle technique with Shamrock method as an alternative regional anesthesia.

NCT ID: NCT03405974 Recruiting - Clinical trials for Osteonecrosis of Femoral Head

Aspirin in the Prevention of Collapse in Osteonecrosis of the Hip

Start date: October 12, 2017
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if prolonged administration of low-dose aspirin will prevent the progression of early-stage osteonecrosis of the femoral head and may even reduce the extent of involvement of the femoral head by the necrotic process The design is intended to be parallel group where a total of 114 patients will be randomized in a 1:1 ratio to the treatment (ASA) and the control (Placebo) arms.

NCT ID: NCT03180463 Suspended - Clinical trials for Osteonecrosis of Femoral Head

The Study of Early Stage Osteonecrosis of Femoral Head With Human Umbilical Cord Mesenchymal Stem Cells (19#iSCLife®-ONFH)

Start date: December 31, 2024
Phase: Phase 1/Phase 2
Study type: Interventional

The purposes of the study is to evaluate the safety and efficacy of human umbilical cord mesenchymal stem cells (hUC-MSC) in treating osteonecrosis of femoral head patients.

NCT ID: NCT02735538 Completed - Clinical trials for Osteonecrosis of Femoral Head

Transcription Factor Runx2 in Necrotic Femoral Head Tissue

Start date: July 2009
Phase: N/A
Study type: Observational

The trial detected mRNA expression of several bone repair-related genes, including Runx2, in the femoral head and neck of patients with osteonecrosis of femoral head (ONFH) . Runx2 expression was compared with that of identical tissue from osteoarthritis patients to identify expression in necrotic femoral head tissue, which will help clarify the role and possible clinical significance of Runx2 in femoral head necrosis, bone repair and reconstruction.

NCT ID: NCT02338596 Completed - Coxarthrosis Clinical Trials

Ultra-Short Anatomic and Conventional Cementless Stems Cementless Stems in Patients Younger Than Fifty-Five Years Old

Start date: June 2001
Phase: Phase 4
Study type: Interventional

As clinical and radiographic performance of an ultra-short anatomic cementless stem have been investigated only two randomized controlled studies, well-designed trials should aim for a thorough comparison of the outcomes of ultra-short and conventional cementless stems. The purpose of this study was to compare the outcomes of ultra-short and conventional stems in the same young patients who underwent simultaneous bilateral sequential total hip arthroplasties.