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Hip Injuries clinical trials

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NCT ID: NCT06087549 Completed - Hip Fractures Clinical Trials

PENG Block vs. ESP Block for Pediatric Hip Surgery

Start date: October 17, 2023
Phase: Phase 4
Study type: Interventional

The study compares the effectiveness and safety of the pericapsular nerve blockade vs. ESPB in pediatric patients who underwent hip surgeries.

NCT ID: NCT05343195 Completed - Hip Injuries Clinical Trials

Balance and Leg Function After Hip Replacement

Start date: March 15, 2021
Phase: N/A
Study type: Interventional

Task-oriented leg exercise are commonly used after joint surgeries in various hip pathologies. Based on this theory, it was hypothesized that task-oriented exercise without conventional physiotherapy can have better result in recovery of balance and leg function than with a conventional post-hip physiotherapy program after hip replacement surgery. The aim of the study was to determine the effect of task-oriented exercise on balance and leg function after total hip replacement.

NCT ID: NCT05245097 Completed - Osteoporosis Clinical Trials

Mitigation of Major Hip Injury Due to Fall With a Smart Belt

Start date: March 29, 2022
Phase: N/A
Study type: Interventional

Multi-center, comparative, non-significant risk adaptive study with retrospective controls. After providing informed consent and being screened for eligibility, intervention subjects will be prescribed and provided an appropriately sized Tango Belt. The subject must demonstrate a minimum of 64% adherence to the use of the Tango Belt within 14 days of initiation to fully enroll in the study. Upon demonstration of at least minimum adherence, the subject will be provided the Tango Belt to wear continuously for at least 6 months, except during bathing, device charging, and as deemed by clinical staff. The study will investigate the safety and effectiveness of the Tango Belt with the primary and secondary endpoints being taken every 3 months and at the end of the study run time from the electronic medical record. Additionally, ancillary endpoints on adverse events and device performance will be gathered.

NCT ID: NCT04210440 Completed - Hip Injuries Clinical Trials

The Treatment of Initial Stage of Hip Osteonecrosis: the Core Decompression

NEC15
Start date: March 1, 2003
Phase: N/A
Study type: Interventional

This retrospective study evaluates 52 cases of avascular necrosis of femoral head (AVN) treated by core decompression, bone chips allograft, fibrin platelet rich-plasma (PRF) and concentrated autologous mesenchymal stromal cells (MSCs).

NCT ID: NCT04169113 Completed - Hip Injuries Clinical Trials

Opiate Prescribing Guidelines Following Hip Arthroscopy

Start date: June 12, 2018
Phase: N/A
Study type: Interventional

The purpose of the study is to determine if opiates are required to achieve appropriate analgesia after hip arthroscopy in outpatient surgery. The investigators hypothesize that patients are frequently prescribed more opiates than are needed after surgery, resulting in excess medications that are at risk for misuse, diversion and contribution to the opioid epidemic

NCT ID: NCT04070430 Completed - Hip Fractures Clinical Trials

Crutch Use After Arthroscopic Hip Surgery

Start date: September 1, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether crutch use for 4 weeks following hip arthroscopic surgery is superior to crutch use for 2 weeks following hip arthroscopic surgery. The primary objective of the study is to compare PRO scores between patients who have used crutches for 2 weeks and patients who have used crutches for 4 weeks.

NCT ID: NCT03959254 Completed - Hip Injuries Clinical Trials

Specific Protocoled Physiotherapy Treatment for Subjects Surgically Treated for Femoroacetabular Syndrome

FAI
Start date: June 19, 2019
Phase: N/A
Study type: Interventional

Physiotherapy treatment protocols described in the bibliography after hip surgery are most of them nonspecific. An experimental study is proposed to determine the effectiveness of a protocolized treatment of physiotherapy in the postoperative treatment of femoroacetabular impingement treated by arthroscopy. This study tries to adapt the non-specific post-surgical physiotherapy treatment protocols of the hip to the characteristics of the femoroacetabular impingement and its arthroscopic surgery.

NCT ID: NCT03855748 Completed - Hip Injuries Clinical Trials

Hip Peak Torque in Running and Jumping Activities in Healthy Active Subjects

Start date: February 27, 2019
Phase:
Study type: Observational

Hip-related groin pain is common in sports that involves change of direction, kicks and sprint accelerations such as football, ishockey, tennis and basketball. Groin pain symptoms either pre- or post-treatment may be load-related, there is limited information on how different sporting activities affect hip joint loading. Thus, the purpose of this explorative cross-sectional study is to investigate hip peak torque in running and jumping activities in healthy active subjects. Such information may guide furture rehabilitation strategies and return to sport sport criteria. Twenty healthy subjects from the Capital Region of Denmark with an age of 18-40 will be included. Hip joint kinetics and kinamatics will be obtained during the following activities for each subjects: 1. Walking 2. Jogging (8-11 km/h) 3. Maximal 6 meters sprint acceleration 4. Single leg drop jump from 35 cm height 5. Horizontal jump with single leg landing with a distance of 100% and 150% of leg length 6. Maximal change of direction at 45, 135, 180 degrees 7. Single-leg cross-country skiing exercise

NCT ID: NCT03571971 Completed - Pain Clinical Trials

Load Modification Versus Standard Exercise for Greater Trochanteric Pain Syndrome

GLAM
Start date: July 17, 2018
Phase: N/A
Study type: Interventional

Greater trochanteric pain syndrome (GTPS), or lateral hip pain, is associated with muscle weakness, altered movement patterns and painful daily activities. The disability associated with GTPS is comparable to end stage hip osteoarthritis, primarily affecting young and middle aged women. Few non-operative treatments have demonstrated long-term lasting or satisfactory results. For those who do improve, recurrence rates of pain and disability can be as high as 50%. Gluteal tendinopathy is the most common condition associated with a GTPS diagnosis. High compressive loads of the gluteal tendons during common activities like walking, stair-climbing, and running are the theorized mechanism for GTPS. These compressive loads are exacerbated with postures and movement patterns that involve the lateral tilting of the pelvis or movement of the thigh across the midline of the body. There is recent evidence that load modification through education and exercise is superior to a corticosteroid injection for reducing pain in these patients. However, it is unknown whether the possible effects of the load modification program were due to exercise alone or the reduction in compressive loads. As current physical therapy interventions for GTPS commonly incorporate high load postures and exercise activities, there is an urgent need to compare outcomes of standard of care physical therapy to load modification. The goal of this study is to evaluate the short-term effects of load modification education on pain and function in individuals with GTPS. Participants will be randomized to receive either standard exercise education or load modification education. Both groups will complete a series of questionnaires about their pain and function, and undergo a brief 2-dimensional assessment of their posture and movement. Between follow-up sessions, participants will be asked to respond to brief weekly online surveys to document their home program compliance, pain, and function. It is hypothesized that the group of participants receiving load modification will have the highest proportion of individuals with significant improvements in pain and function, and will demonstrate improved posture and movement.

NCT ID: NCT03527407 Completed - Hip Injuries Clinical Trials

MIDAS: Minimal-dataset for the Assessment of Surgical Outcomes - Potential in Hip Surgery

MIDAS
Start date: July 1, 2017
Phase:
Study type: Observational

Swiss legislation requires health service providers to collect such information. of medical quality indicators as part of the quality and performance audit (Article 22a KVG). In addition, comparisons of clinics or specialist specialists on cost and quality of results are required (Art. 49 (8)). Currently, the quality of a medical therapy is evaluated rather negatively on the absence (or occurrence) of complications. In contrast, however, the goal of therapy must be to improve or maintain the health-related quality of life (HRQoL). Accordingly, the Swiss Society of Surgery (SGC-SSC), in collaboration with the Association for Quality Assurance in Surgery (AQC), has developed a minimum dataset designed to assess the quality of life of patients after surgical intervention. In order to enable Switzerland to be comparatively independent of the discipline, generic (in the Research Plan - MIDAS -V2, date 24.05.2017 Page 5/57 Contrary to disease-specific) survey instruments proposed that cover the general quality of life in its different facets, regardless of the function of individual organ systems. The complication documentation was not completely abandoned in this proposal, but is only a quality indicator among many due to patient-related outcome measurements. However, the development of a minimal data set with quality indicators that are applicable across all surgical sub-disciplines for evaluating the quality of treatment of acute and chronic diseases raises a number of fundamental questions that can only be answered to a limited extent without empirical studies. Five essential questions are: I. Is it sufficient to work with generic quality of life tools or is it necessary to use disease / indication specific instruments or functional tests? II. Which is the best, solid time for a follow-up? III. Is it possible and useful to make a third-party determination of the quality of life in patients with limited cognitive abilities? IV. Which preoperative risk factors should be documented so that sufficient adjustment for case mix differences in hospital comparisons can be made? V. Which perioperative and postoperative factors, in particular complications, must be raised beyond the quality of life, as they reflect an independent aspect of quality?