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Arthropathy of Hip clinical trials

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NCT ID: NCT03185117 Terminated - Opioid Use Clinical Trials

Opioid Consumption After Hospital Discharge in Orthopedic Surgery

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

At the Ohio State University, and across the country, surgical patients admitted to the hospital are over-prescribed a significant amount of opioid medications upon discharge to home. Recent studies reveal that a large percentage of patients prescribed opioid medications after surgery have approximately half of the prescribed medication left over. This study aims to evaluate reported opioid use after surgery in patients undergoing major orthopedic surgery in order to better approach the issue with current opioid use and abuse trends while still providing adequate medical care and pain management to patients

NCT ID: NCT03079479 Completed - Clinical trials for Arthroplasty Complications

Impact on Muscle Strength, Quality of Life and Functionality in Individuals Submitted to Hip Arthroplasty: a Prospective Study.

Start date: July 1, 2016
Phase:
Study type: Observational

Introduction: Total hip arthroplasty has been increasingly used as a means of treating the various pathologies of this joint. However, this surgical reconstruction initially brings important deficits in subjects submitted, such as: inhibition of muscle strength, limitation of range of motion and functional deficit. Therefore, an immediate physiotherapeutic treatment is necessary in the short and long term, taking into account both biomechanical issues and the quality of life of these individuals. Objective: To evaluate the clinical evolution of individuals submitted to total hip arthroplasty in the ten year period. Method: Twenty individuals submitted to unilateral total hip arthroplasty will be evaluated by the medical group of hip surgeries of the Brotherhood of Santa Casa de Misericórdia of São Paulo, during a period of ten years. These individuals will undergo a primary clinical evaluation and after signing the consent form, will be evaluated functionally with the HARRIS HIP SCORE and WHOQOL-bref questionnaires and physically with the analysis of muscular strength through manual dynamometry to measure the strength level of the Muscles involved in the bilateral coxo-femoral joint, such as abductors, adductors, flexors, extensors, internal rotators, external rotators, knee joint, such as extensors and flexors, and ankle, plantar flexors. Finally, they will be referred to the kinematic gait analysis, to identify the functional characteristics of these individuals, through reflexive markers at specific anatomical points, where they will walk for 5 minutes on a treadmill at a speed of 1.5km per hour.

NCT ID: NCT02884388 Recruiting - Arthropathy of Hip Clinical Trials

A Combined Nerve Block in Elderly Patients Subjected to Total Hip Replacement

Start date: December 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to validate the hypothesis that a combined nerve block produces better outcomes including intraoperative stress, hemorrheological indexes, postoperative immune function, and incidence of postoperative complications than general anesthesia.

NCT ID: NCT02884349 Recruiting - Arthropathy of Hip Clinical Trials

The Relationship Between Component Position and RoM

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

The aim of the study is to determine the influence of the combined anteversion of acetabular cup and the femoral stem used in total hip arthroplasty on the theoretical and actual range of motion of the hip in three dimensional space.

NCT ID: NCT02645435 Completed - Surgery Clinical Trials

Consequence of the Learning Curve in Direct Anterior Approach for Total Hip Replacement

Start date: December 2015
Phase: Phase 4
Study type: Interventional

Background: Direct anterior approach to the hip (DAA) is being considered as one of the most promising minimally-invasive approaches in total hip arthroplasty (THA). Purpose of this study is to analyse influence of learning curve on clinical and radiographic outcome in direct anterior approach (DAA) for total hip replacement. Methods: The first 30 patients operated with DAA (group B) were compared to 39 patients operated by Hardinge approach (group A). Peri-and postoperative complications, Harris Hip Score (HHS), implant positioning, experienced pain and patient satisfaction were evaluated at a mean follow-up of 32 months.

NCT ID: NCT02619409 Completed - Arthropathy of Knee Clinical Trials

Evaluation of the Duration of Bupivacaine Spinal Block in Orthopedic Procedures With and Without Epinephrine Wash

Start date: February 11, 2016
Phase: N/A
Study type: Interventional

Bupivacaine spinal is commonly performed as the primary anesthetic for orthopedic procedures. In some cases the duration of the block is inadequate. An epinephrine wash is sometimes performed to prolong the duration of the block. The epinephrine wash may prolong the duration of the block, and if it does, to what extent?

NCT ID: NCT02584725 Completed - Arthropathy of Knee Clinical Trials

Tranexamic Acid Dosing for Total Joint Arthroplasty

Start date: December 2014
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the effect of increasing doses of tranexamic acid (TXA) on limiting blood loss during total knee and total hip arthroplasty as defined by a change in hemoglobin from pre-operative baseline to the first post-operative day.

NCT ID: NCT02493621 Completed - Arthropathy of Hip Clinical Trials

Compare Epidural vs. Lumbar Plexus Analgesia After Hip Arthroplasty

Start date: December 2014
Phase:
Study type: Observational

The goal of this retrospective chart review is to evaluate if the implementation of lumbar plexus block placement for postoperative pain have improved conditions in the postoperative period for patients undergoing total hip arthroplasty when compared to the placement of epidurals for postoperative pain management.

NCT ID: NCT02404727 Completed - Osteoarthritis, Hip Clinical Trials

Evaluation of Cemented and Cementless Fixation of Dual-mobility Hip Prosthesis in Elderly Patients With Osteoarthritis

Start date: October 2014
Phase: N/A
Study type: Interventional

The aim of this project is to investigate prosthesis fixation in the bone, respectively cemented and uncemented operation method of Avantage® dual-mobility acetabular cup in elderly patients, wear of the plastic in dual-mobility hip prosthesis and evaluate the clinical function, patient satisfaction and possible complications. Patients included in this study suffer from osteoarthritis of the hip.

NCT ID: NCT01684631 Completed - Arthropathy of Hip Clinical Trials

Evaluation of Implant Survival in Patients With a Pinnacle Ultamet Device in Conventional Total Hip Joint Replacement

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

The objective is to evaluate the implant survival rate for patients implanted with a PINNACLE® ULTAMETâ„¢ Metal-on-Metal implant for conventional total hip arthroplasty for the treatment of a severe hip disease and true femoral cervical fracture.