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Arthroplasty Complications clinical trials

View clinical trials related to Arthroplasty Complications.

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NCT ID: NCT05060536 Recruiting - Clinical trials for Arthroplasty Complications

Infrapatellar Fat Pad Excision in Total Knee Arthroplasty

Start date: August 31, 2021
Phase: N/A
Study type: Interventional

To examine whether removing the infrapatellar fat pad from the knee during total knee arthroplasty affects the patient outcome in terms of pain and knee function following the procedure. Currently there is no consensus on whether removing this tissue from the knee has a positive or detrimental effect. Small studies have been published, some showing improved symptoms and some worse symptoms. Current practice of orthopaedic surgeons is either to routinely remove or routinely retain the tissue when performing total knee arthroplasty.

NCT ID: NCT05028426 Completed - Clinical trials for Arthroplasty Complications

Safety of Total Knee Replacement Surgery Before and After the Implementation of Enhanced Recovery Program

Start date: January 2015
Phase:
Study type: Observational

The objectives are to describe the transition from traditional care to an enhanced recovery program for the management of total knee arthroplasty, and to evaluate the effect on patient outcomes.

NCT ID: NCT05014932 Not yet recruiting - Clinical trials for Arthroplasty Complications

Evaluation of Noise Induced by Ceramic-ceramic Friction Torques of Total Hip Prostheses With Customized Femoral Stem

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

Evaluation of noise induced by ceramic-ceramic friction torques of total hip prostheses with customized femoral stem. Retrospective and prospective multicentric study.

NCT ID: NCT05013879 Completed - Clinical trials for Arthroplasty, Replacement, Knee

Kinesiotape for Edema After Bilateral Total Knee Arthroplasty

Start date: October 18, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if kinesiotaping for edema management will decrease post-operative edema in patients with bilateral total knee arthroplasty. The leg receiving kinesiotaping during inpatient rehabilitation may have decreased edema and pain and improved movement and function when compared to the leg not receiving kinesiotape.

NCT ID: NCT04913623 Recruiting - Clinical trials for Arthroplasty Complications

Correlation of Intramedullary Pressure and Systemic Inflammatory Parameters in Cemented Femoral Stem

Start date: March 23, 2021
Phase:
Study type: Observational

The cemented femoral stem have impact on increase on systemic parameters. Evaluation of the level of histamine, C-reactive protein (CRP) and leukocytes formula, IL1b, TNF alpha, IL6 and the reflection of changes of these parameters in the intra-operative course of hip replacement.

NCT ID: NCT04821154 Recruiting - Knee Osteoarthritis Clinical Trials

Persona Revision Knee System Outcomes

Start date: June 14, 2021
Phase:
Study type: Observational

The study will evaluate the performance, clinical benefits and safety of the Persona Revision Knee System in patients who have received primary or revision total knee arthroplasty (TKA) treatment. This will be done using a multicenter, single-arm, consecutive series, retrospective cohort study with prospective follow-up.

NCT ID: NCT04810000 Completed - Clinical trials for Arthroplasty Complications

The Effect of Releasing the Tourniquet in Total Knee Replacement Before Closure on the Blood Loss , Joint Effusion , Hematoma Formation and Wound Complication

Start date: December 3, 2018
Phase:
Study type: Observational [Patient Registry]

The study , observe the effect of releasing the Tourniquet in total knee replacement surgery before closure in comparison with releasing it after wound closure The effect was assessed by Hb drop post operative and Hematoma formation ( measured by ultrasound ) as well as the wound complication

NCT ID: NCT04772625 Active, not recruiting - Knee Osteoarthritis Clinical Trials

Failure Analysis of Patellofemoral Arthroplasty

Start date: January 1, 2019
Phase:
Study type: Observational

The purpose of the retrospective cohort study is 1) to determine preoperative risk factors for revision af patellofemoral arthroplasty, and 2) to provide a detailed description of indications for revision after patellofemoral arthroplasty. All patients operated with patellofemoral arthroplasty in Denmark from January 1, 2008 to December 31, 2015, will be included in the cohort.

NCT ID: NCT04707001 Recruiting - Clinical trials for Arthroplasty Complications

Urinary Retention After Arthroplasty

UREA
Start date: May 1, 2021
Phase: N/A
Study type: Interventional

Arthroplasty increases the risk of postoperative urinary retention. Treatment of postoperative urinary retention is indwelling or intermittent catheterization. The need for catheterization is most commonly determined with an ultrasound scanner. Catheterization increases the risk of urinary tract infection, which may further lead to haematogenic infection of the artificial joint. There is no evidence of an optimal way to monitor the onset of spontaneous urination. The aim of the study is to determine whether monitoring the onset of spontaneous urination after fast track knee arthroplasty is safe based on symptoms alone without ultrasound monitoring.

NCT ID: NCT04691362 Completed - Clinical trials for Arthroplasty Complications

Noninferiority Oral Tranexamic Acid vs Intravenous Administration in Total Hip Arthroplasty

Start date: January 1, 2021
Phase: Phase 4
Study type: Interventional

To find noninferiority relationship between oral and intravenous administration of tranexamic acid on peroperative and postoperative blood loss and serum concentration during primary total hip arthroplasty.