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Arthroplasty clinical trials

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NCT ID: NCT06371833 Not yet recruiting - Arthroplasty Clinical Trials

PRIMA EU Retrospective & Prospective

Start date: May 2024
Phase:
Study type: Observational

This clinical study aims at evaluating clinical, radiographic and patient-reported outcomes after total anatomic or reverse shoulder replacement using PRIMA humeral stem up to 24 months after surgery, in order to assess the short-term performance of the implant. Furthermore, the objective is also to collect short-term data on the survivorship of the implant and the incidence of complications.

NCT ID: NCT06323980 Not yet recruiting - Arthroplasty Clinical Trials

INHANCE Stemless Reverse Shoulder IDE

Start date: September 30, 2024
Phase: N/A
Study type: Interventional

2:1 Randomized, Controlled, Multi-Center, Prospective, Pre-Market Study of the INHANCE Stemless Reverse Cementless Total Shoulder.

NCT ID: NCT06264999 Not yet recruiting - Arthroplasty Clinical Trials

Robotic Assisted Knee Arthroplasty - Retain the Anterior Cruciate Ligament or Not

Start date: March 2024
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to compare the function of the knee after retaining or sacrificing the anterior cruciate ligament in robotic assisted knee arthroplasty. The main questions it aims to answer are: Does retaining the anterior cruciate ligament improve postoperative gait? Participants will perform - Gait analysis - Stair performance test - CT based Micromotion analysis of the implant micromovement

NCT ID: NCT05971641 Not yet recruiting - Arthroplasty Clinical Trials

The Effect of Progressive Relaxation Exercises on Postoperative Pain

Start date: December 1, 2023
Phase: N/A
Study type: Interventional

The indicators of patient recovery in the postoperative period include sleep, physical functionality, mental health, cognitive functionality, pain, and psychosocial functionality. This thesis aims to investigate the effects of progressive relaxation exercises on postoperative pain intensity, sleep quality, and recovery in patients undergoing total knee arthroplasty.This study, designed as a randomized controlled experimental study, will be conducted between September 1, 2023, and August 1, 2024, at ÇAYCUMA State Hospital in ZONGULDAK province, Turkey, among patients undergoing total knee arthroplasty. A total of 96 patients will be recruited based on the sample size calculated using G-power analysis. Through block randomization, 48 patients will be assigned to the intervention group and 48 patients to the control group. Data will be collected using the Numeric Rating Scale for pain, the Richard-Campbell Sleep Scale, a sleep tracker smart wristband to measure sleep quality and duration, the Postoperative Recovery Index, and a Patient Information Form.

NCT ID: NCT05314387 Not yet recruiting - Clinical trials for Rheumatoid Arthritis

S-11 SMR TT Hybrid Glenoid and Cementless Finned Short Stem

Start date: April 2022
Phase:
Study type: Observational

Post-market, prospective, non randomized, open label, multicentre, clinical study analysing outcomes of shoulder arthroplasty with SMR TT Hybrid Glenoid with or without SMR Cementless Finned Short Stem

NCT ID: NCT05015101 Not yet recruiting - Arthroplasty Clinical Trials

Evaluation of the Clinical and Radiological Outcome of Uncemented Femoral Stems According to Their Proximal Coating

ETNA
Start date: September 2021
Phase:
Study type: Observational

Evaluation of the clinical and radiological outcome of uncemented femoral stems according to their proximal coating. Retrospective study

NCT ID: NCT04906681 Not yet recruiting - Neurologic Disorder Clinical Trials

Implementation of a Rehabilitation Technology in Orthopedic and Neurological Rehabilitation to Increase Therapy Dosage: an Exploratory Study

Start date: September 1, 2021
Phase: Phase 1/Phase 2
Study type: Interventional

Rehabilitation technology is more and more implemented in conventional therapy to increase the dosage of therapy and/or increase patient's motivation towards therapy. In orthopedic as well as neurological rehabilitation it is important to exercise with enough intensity and repetitions to improve functional performance in activities of daily life, and consequently quality of life. At the moment, not all (rehabilitation) technologies are adapted towards the wishes and needs of both patients and therapists for everyday use in the clinical setting. Also, not all technologies are fit for independent use by the patients. Researcher of PXL have developed a Kinect-based system (i.e. i-ACT) for rehabilitation and performed supervised research with i-ACT in neurological and musculoskeletal rehabilitation, and older adults. Within this research, patients will exercise with i-ACT under supervision of their therapist during weekdays, but in the weekends they will be motivated by the medical staff to perform their exercises with i-ACT. The medical staff will be present for safety reasons, but the patient is asked to use and exercise with i-ACT as independent as possible. The aim of this research is to explore to which extend i-ACT is suitable for semi-independent use by patients in orthopedic or neurological rehabilitation.

NCT ID: NCT04219098 Not yet recruiting - Arthroplasty Clinical Trials

Pain After Preoperative UltraSound Guided Hip Injections for Total Hip Arthroplasty (PUSH)

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

The purpose of the study is to assess the accuracy of Butterfly IQ ultrasound for intra-articular hip injections, and to see if an injection given intra-articular before incision provides any benefit in preemptive pain relief or blood loss reduction.

NCT ID: NCT03476148 Not yet recruiting - Clinical trials for Osteoarthritis, Knee

Home Rehabilitation Using Interactive Device Versus Inpatient Rehabilitation in Total Knee Arthroplasty

Start date: March 22, 2018
Phase: N/A
Study type: Interventional

Rehabilitation after total knee arthroplasty is very important in terms of range of motion of the knee, muscle power, normal gait, pain control and consequently the patient's satisfaction. Convectional rehabilitation methods in assist of therapist required high demand of resources. Recently, outpatient clinic or tele-communication tool based rehabilitations were investigated and reported equivalent results. However, those methods also required group or one-to-one facing that restricted availability of the exercise. With development of the motion tracking technology, new device that gives real time feedback with augmented reality images can be used for rehabilitation in home-based setting. This study aims to compare the clinical outcomes after the rehabilitation by interactive home-based device or conventional inpatient setting.

NCT ID: NCT02465684 Not yet recruiting - Arthroplasty Clinical Trials

Effect of Tourniquet on UKA

Start date: November 2016
Phase: N/A
Study type: Interventional

There is obviously a lack of evidence regarding the risk-benefit ratio of a thigh tourniquet in unicondylar knee arthroplasty (UKA). This refers to many possible outcome criteria like operating time, blood loss, quality of prosthesis fixation in the bone, adverse events, radiographic result, clinical score outcome, easy of rehabilitation etc. It is not appropriate to rely on findings from the field of total knee arthroplasty. It is the aim of the current study, to clarify the role of a thigh tourniquet during UKA with regard to component fixation quality, component positioning and sizing, clinical outcome and rehabilitation process. Patients scheduled for routine UKA implantation due to osteoarthritis or osteonecrosis in the medial compartment will be considered for participation. Patients are then randomized for surgery with or without tourniquet. After an anteromedial Quad-Sparing approach the UKA procedure itself is then carried out, as suggested by the manufacturer. For both groups puls lavage and meticulous drying is applied before cementing. The following outcome parameters are assessed: 1)radiographic cement mantle thickness, 2)component position & sizing, 3)diolucencies, 4)score outcome and 5)parameters of early Rehab.