- Trials with a EudraCT protocol (294)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
294 result(s) found for: Hip bone.
Displaying page 1 of 15.
EudraCT Number: 2016-000926-21 | Sponsor Protocol Number: AMSC-BDT-002 | Start Date*: 2016-10-06 | |||||||||||
Sponsor Name:Fakultní nemocnice Hradec Králové | |||||||||||||
Full Title: Innovation of method cryopreservation for clinical use autologous multipotent mesenchymal stem cells (MSCs) for treatment of extensive skeletal defects in revision surgery of total hip arthroplasty+ | |||||||||||||
Medical condition: Revision total hip arthroplasty | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000628-14 | Sponsor Protocol Number: ISS20109714 | Start Date*: 2013-09-13 | |||||||||||
Sponsor Name:Turku University Hospital | |||||||||||||
Full Title: Denosumab in enhancement of bone bonding of hip prosthesis in postmenopausal women: a randomized, double-blind, placebo-controlled study | |||||||||||||
Medical condition: Hip osteoarthritis | |||||||||||||
|
|||||||||||||
Population Age: Elderly | Gender: Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001725-25 | Sponsor Protocol Number: RSA-HIP220306 | Start Date*: 2007-08-09 | |||||||||||
Sponsor Name:GREATER GLASGOW HEALTH BOARD | |||||||||||||
Full Title: REVISION HP REPLACEMENT - ACETABULAR IMPACTION GRAFTING - A RADIOSTEREOMETRIC COMPARISON BETWEEN FRESH FROZEN ALLOGRAFT AND MARROW-DEPLETED BONE WITH CALCIUM PHOSPHATE PLUS OR MINUS BONE MORPHOGENI... | |||||||||||||
Medical condition: REVISION HIP REPLACEMENT | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005599-33 | Sponsor Protocol Number: AMSC-BDT-001 | Start Date*: 2013-06-10 | |||||||||||
Sponsor Name:Lékařská fakulta Univerzity Karlovy v Hradci Králové | |||||||||||||
Full Title: Utilization of Autologous Multipotent Mesenchymal Stem Cells in the Management of the Large Skeletal Defects during Revision Total Hip Arthroplasty: a Prospective, Non-randomized, Open-Label Study ... | |||||||||||||
Medical condition: Revision total hip arthroplasty. | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000654-38 | Sponsor Protocol Number: AHUS2015-000654-38 | Start Date*: 2015-10-19 | |||||||||||
Sponsor Name:Akershus University Hospital, Norway | |||||||||||||
Full Title: Secondary prophylaxis after hip fracture. An evaluation og two organisational models based on choise of treatment: a comparison of efficacy and applicability of hospital based treatment with zoled... | |||||||||||||
Medical condition: Hip fracture | |||||||||||||
|
|||||||||||||
Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001481-18 | Sponsor Protocol Number: 6925 | Start Date*: 2011-10-07 |
Sponsor Name:Uppsala University Hospital | ||
Full Title: Uncemented total hip implant and subcutaneous injection of Denosumab for patients with osteoarthritis of the hip. A randomised double blind placebo controlled study on the effects on bone evaluated... | ||
Medical condition: Patients with osteoarthritis of the hip treated with an uncemented total hip arthroplasty. This procedure is accompanied with an increased risk for loss of bone adjacent to the implants | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-001708-14 | Sponsor Protocol Number: ABOGRAFT-01 | Start Date*: 2021-06-29 |
Sponsor Name:Region Östergötland | ||
Full Title: Antibiotic Impregnated Bone Graft to reduce infection in hip replacement. The ABOGRAFT trial | ||
Medical condition: Patients scheduled for any type of hip arthroplasty requiring bone grafting | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2006-002557-68 | Sponsor Protocol Number: CDJN608 FI01 | Start Date*: 2006-11-06 |
Sponsor Name:Hospital District of Southwest Finland | ||
Full Title: A randomized, double-blind, placebo-controlled study to evaluate the efficacy of zoledronic acid in enhancement of early stability of cementless primary hip prosthesis | ||
Medical condition: Bone loss occurring around cementless hip prosthesis in postmenopausal women treated for primary hip osteoarthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-013777-17 | Sponsor Protocol Number: 1 | Start Date*: 2010-02-08 |
Sponsor Name:Central Manchester and Manchester University Children's Hospital NHS Trust.
[...]
1. Central Manchester and Manchester University Children's Hospital NHS Trust.
2. |
||
Full Title: The effect of pamidronate treatment on bone health in patients with neuromuscular disease undergoing hip surgery. | ||
Medical condition: Children with neuromuscular conditions undergoing hip surgery. Aiming to identify whether pamidronate a licenced medicine mainatins bone mineral density in patients with neuromuscular conditions un... | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2009-014414-98 | Sponsor Protocol Number: 58185 | Start Date*: 2009-10-29 |
Sponsor Name:Department of Orthopaedic Surgery University Hospital Linköping | ||
Full Title: The impact of local bisphosphonate treatment on prosthetic fixation | ||
Medical condition: Osteoarthritis of the hip joint treated with total hip replacement | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-002965-19 | Sponsor Protocol Number: 1 | Start Date*: 2005-03-14 |
Sponsor Name:Orthopaedic department, Karolinska Institutet, Danderyd's Hospital | ||
Full Title: Can risedronate prevent periprosthetic bone loss after hip arthroplasty? A randomized, double-blind, placebo-controlled trial | ||
Medical condition: Periprosthetic bone loss after total hip arthroplasty (THA) is the main factor in limiting the longevity of implants used för treatment of osteoarthritis. Bone loss leads to implant destabilization... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-001543-13 | Sponsor Protocol Number: HIP-SAP | Start Date*: 2018-03-28 | ||||||||||||||||||||||||||
Sponsor Name:Morten Tange Kristensen/Hvidovre Hospital | ||||||||||||||||||||||||||||
Full Title: Preliminary effect and safety of physiotherapy with strength training and protein-dense nutritional supplement in combination with anabolic steroids in cross-continuum rehabilitation of patients wi... | ||||||||||||||||||||||||||||
Medical condition: Area of investigation is recovery of muscle strength and function following hip fracture surgery. | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
Population Age: Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-000638-17 | Sponsor Protocol Number: 44107 | Start Date*: 2021-03-30 |
Sponsor Name:Oslo University Hospital | ||
Full Title: ZOLEDRONATE EARLY TO HIP FRACTURE PATIENTS – SAFE AND EFFECTIVE? A DOUBLE-BLINDED RANDOMIZED CONTROLLED TREATMENT STRATEGY TRIAL ON ZOLEDRONATE IN HIP FRACTURE PATIENTS THE ZEBRA TRIAL | ||
Medical condition: Osteoporosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2016-000377-20 | Sponsor Protocol Number: VK5211-201 | Start Date*: 2016-05-27 | |||||||||||
Sponsor Name:Viking Therapeutics, Inc. | |||||||||||||
Full Title: A Phase II, Randomized, Double-Blind, Parallel Group, Placebo- Controlled, Multi-Center Study to Explore the Efficacy, Safety and Tolerability of VK5211 in Subjects with Acute Hip Fracture | |||||||||||||
Medical condition: Hip fracture | |||||||||||||
|
|||||||||||||
Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000541-20 | Sponsor Protocol Number: STH15714 | Start Date*: 2011-09-20 | |||||||||||
Sponsor Name:Sheffield Teaching Hospitals NHS Foundation Trust | |||||||||||||
Full Title: Effect of Denosumab on Osteolytic Lesion Activity in Total Hip Arthroplasty (THA) | |||||||||||||
Medical condition: Prosthesis-related osteolysis after total hip arthroplasty | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004445-42 | Sponsor Protocol Number: 1 | Start Date*: 2007-05-22 |
Sponsor Name:Institut for Pharmacology and Toxicology | ||
Full Title: Pharmacokinetics of Cetriaxon in bone | ||
Medical condition: hip replacement | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-003898-42 | Sponsor Protocol Number: 2 | Start Date*: 2008-03-19 |
Sponsor Name:Institut for Pharmacology and Toxicology | ||
Full Title: Pharmacokinetica of levofloxacine in bone | ||
Medical condition: hip or knee replacement | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2009-012929-11 | Sponsor Protocol Number: PREOB-ON3 | Start Date*: 2011-10-17 | |||||||||||
Sponsor Name:Bone Therapeutics S.A. | |||||||||||||
Full Title: Phase III, pivotal, multicentre, randomised, double-blind controlled Study to evaluate the Efficacy and Safety of Autologous Osteoblastic Cells (PREOB®) Implantation in Early Stage Non Traumatic Os... | |||||||||||||
Medical condition: Osteonecrosis of the Femoral Head | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) DE (Completed) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011920-69 | Sponsor Protocol Number: 0822-043-00 | Start Date*: 2011-08-05 |
Sponsor Name:Merck & Co., Inc. | ||
Full Title: A Quantitative Computed Tomography (QCT) Sub-Study of the Phase III Randomized, Placebo-Controlled Clinical Trial to Assess the Safety and Efficacy of Odanacatib (MK-0822) to Reduce the Risk of Fra... | ||
Medical condition: postmenopausal osteoporosis | ||
Disease: | ||
Population Age: Elderly | Gender: Female | |
Trial protocol: NO (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-001906-41 | Sponsor Protocol Number: CHUBX2019/24 | Start Date*: 2021-06-16 |
Sponsor Name:CHU DE BORDEAUX | ||
Full Title: Benefit of positons emission tomography / 68Gallium citrate tomodensitometry for artificial hip and knee chronic infection diagnosis | ||
Medical condition: joint prosthesis infection | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
• EEA CTAs: Date study was authorised to proceed
• Outside EU/EEA: Date study was submitted in EudraCT
• Outside EU/EEA: Date study was submitted in EudraCT
