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Hip Dislocation clinical trials

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NCT ID: NCT05238935 Recruiting - Clinical trials for Developmental Dysplasia of the Hip

Do All Patients With Congenital Hip Dysplasia Corrected Operatively Need Physiotherapy

Start date: February 23, 2022
Phase: N/A
Study type: Interventional

Developmental Dysplasia of the Hip (DDH) is a common condition among young children that could range in severity. in most sever cases, surgical intervention is the best choice to correct the hip abnormality with the aim of restoring optimal functional ability. Referring patient for physiotherapy treatment post operative is not a common practice and surgeons relay on children natural developmental milestone in their recovery. however, prescribed physiotherapy treatment could promote maximum functional recovery and wellness. the aim of this research is (1) to evaluate the functional deference between patients who had conventional physiotherapy treatment program and patients who had home program prescribed by the orthopedic surgeon (2) to investigate what might be the underlying risk factors that could enhance or prohibit satisfactory functional level post operatively. all individuals diagnosed with DDH and operated by Dr. Saleh Alsaifi (an orthopedic surgeon at alrazi orthopedic hospital) will be invited to participate in this study. The study will look at the children development in fictional ability postoperatively. not being referred to physiotherapy is a common practice, so the patients in the intervention group will benefit from having regular physiotherapy treatment with no risk at all. the study run from Alrazi orthopedic hospital in kuwait. the research is a collaboration between an orthopedic surgeon (Dr. Saleh Alsaifi) and physiotherapy team and it is expected to recruit all of the eligible patients through 12 months period (approximately 50 patients) then, the data will be sorted for analysis and reporting. the study is not funded with no personal interest.

NCT ID: NCT05149729 Recruiting - Hip Arthropathy Clinical Trials

Mid-Term Natural Course Postoperative of Crowe Type III-IV Hip Dysplasia

Start date: February 10, 2021
Phase: N/A
Study type: Interventional

Comparison of preoperative and postoperative mid-term course of patients with Crowe Type 3 and Type 4 hip dysplasia.

NCT ID: NCT04993638 Recruiting - Hip Fractures Clinical Trials

Post Market Clinical Follow-up of Dual-mobility Acetabular Cup EUROSCUP MOBILE

Start date: June 1, 2021
Phase:
Study type: Observational

EUROSCUP MOBILE is intended for use in primary and revision total hip replacement surgery. Hip replacement is intended to provide increased patient mobility and reduce pain by replacing the damages hip joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components. As part of post market vigilance, EUROS will collect data on EUROSCUP MOBILE performances and safety

NCT ID: NCT04795843 Recruiting - Hip Dysplasia Clinical Trials

Exercise and Patient Education Compared With Usual Care in Patients With Hip Dysplasia

MovetheHip
Start date: April 16, 2021
Phase: N/A
Study type: Interventional

This effectiveness trial will investigate if patients with hip dysplasia randomised to exercise and patient education have a different mean change in self-reported pain measured by the Copenhagen Hip and Groin Outcome Score (HAGOS) compared with those randomised to usual care over a six-month follow-up period. Participating patients will be allocated to either exercise and patient education or usual care. Alongside this, a health-economic study and a process-evaluation study will be conducted.

NCT ID: NCT04375345 Recruiting - Hip Osteoarthritis Clinical Trials

DELTA Multihole TT Study

Start date: January 23, 2020
Phase:
Study type: Observational

A retrospective study evaluating clinical and radiographic early outcomes of total hip arthroplasty and revision hip arthroplasty with DELTA Multihole TT cup.

NCT ID: NCT04349046 Recruiting - Clinical trials for Rheumatoid Arthritis

Exception Cementless Hip Stem

Exception
Start date: January 1, 2021
Phase:
Study type: Observational

This study is a multicenter, retrospective and prospective, non-controlled, non-randomized post market clinical follow-up study. The objectives of this study are to confirm the long-term safety, performance and clinical benefits the Exception Cementless femoral stem (standard and varized) when used in primary total hip arthroplasty.

NCT ID: NCT04117685 Recruiting - Clinical trials for Congenital Hip Dysplasia

Global Hip Dysplasia Registry

GHDR
Start date: September 1, 2016
Phase:
Study type: Observational

Developmental dysplasia of the hip (DDH) is the most common hip condition affecting infants and children. DDH represents a spectrum of issues affecting the hip joint - a "ball-and-socket" joint. When the femoral head (the "ball) is seated properly in the acetabulum (the "socket"), the hip is stable and can develop normally. However, when the femoral head is not well-seated, the hip can become unstable or dislocate. This instability or dislocation of the femoral head prevents the hip joint from developing normally during infancy and early childhood. If left undetected or untreated, it can lead to debilitating complications later in life. Development of a comprehensive, prospective international registry for all infants and children with DDH will provide the potential to impact all infants born, not only in British Columbia, but around the world. The purpose of this initiative is to identify best practices and standardize treatment and management strategies in order to optimize clinical and functional outcomes for patients with DDH. This registry includes targeted specific outcomes that will be investigated, in addition to the general collection of data on all patients diagnosed with any form of DDH up to the age of 10 years.

NCT ID: NCT04092634 Recruiting - Dislocation, Hip Clinical Trials

Dual Mobility in "High Risk" Patients

Start date: November 1, 2017
Phase: Phase 4
Study type: Interventional

The aim of this study is to compare clinical outcomes of patients considered to be high risk for prosthetic dislocation undergoing primary total hip arthroplasty (THA) with the use of a dual mobility bearing versus a conventional, single bearing design.

NCT ID: NCT04090359 Recruiting - Dislocation, Hip Clinical Trials

Dual Mobility Acetabular Cups in Revision TJA

Start date: September 1, 2017
Phase: Phase 4
Study type: Interventional

The aim of this study is to the compare clinical outcomes of patients undergoing a revision total hip arthroplasty (THA) with the use of a dual mobility bearing versus a single bearing design with the use of a large femoral head (36mm or 40mm). We hypothesize the use of dual-mobility components in revision THA will be associated with a lower dislocation rate in the first year following surgery.

NCT ID: NCT04080466 Recruiting - Osteoarthritis Clinical Trials

Cam Type FAI is a Cause of Hip Pain in the Young Adult and a Precursor to OA

Start date: February 20, 2021
Phase: Phase 2
Study type: Interventional

An abnormally formed hip joint (cam deformity) is a major cause of osteoarthritis (OA). Individuals may not experience any symptoms until OA is severe due to extensive cartilage loss and changes in underlying bone. A series of studies showed that the cam deformity can lead to the development of OA if left untreated, thus strongly suggesting a causal relationship. Currently, the cam deformity that causes pain is surgically removed to relieve the pain and treat the associated cartilage damage. Recent studies have demonstrated that surgical treatment leads to bone and cartilage changes that were related to improved function and reduced pain.