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Active clinical trials for "Osteoarthritis, Hip"

Results 441-450 of 520

Pain and Sensation After Regional Anesthesia - Pilot Study

AnesthesiaConduction2 more

This study aims to determine spinal resolution and pain levels after the placement of a lumbar plexus block (LPB) and spinal for total hip replacement procedure. This is a pilot study that looks to collect information in order to design a larger, more significant study comparing Quadratus Lumborum blocks (QLB) and Lumbar Plexus blocks.

Completed3 enrollment criteria

Face to Face or Digitally Delivered First-line Osteoarthritis Treatment?

Hip OsteoarthritisKnee Osteoarthritis

This study will compare outcomes of two different delivery methods (Face-to-face and digitally) of first-line treatment for hip and knee osteoarthritis.

Completed5 enrollment criteria

Study on Costs and Effects of Waiting Time in Total Hip and Knee Replacements

OsteoarthritisHip2 more

The aim of this study is to compare the cost-effectiveness of major joint replacement in patients with short and non-fixed (control group) waiting time (WT). After being placed on the waiting list, patients will be randomized into two groups through regular contact with the practice staff: (1) Patients with non-fixed waiting time (patient undergoes hospital's normal procedure from the date (s)he is added to the waiting list to the date of operation), and (2) patients with short waiting time (operated in maximum three months). The main question is: is it possible to improve the cost-effectiveness of major joint replacement by shortening waiting time?

Unknown status10 enrollment criteria

Addressing Patients' Expectations of Total Hip Arthroplasty in a Randomized Trial

Hip OsteoarthritisArthroplasty2 more

The goals of this study are to develop and test an educational intervention to address patients' expectations of long-term outcomes of total hip arthroplasty.

Completed2 enrollment criteria

Avenir Müller Hip Stem Post Market Surveillance Study

OsteoarthritisHip6 more

This study is a Post Market Clinical Follow up study to fulfil the post market surveillance obligations according to Medical Device Directive and European Medical Device Vigilance System (MEDDEV) 2.12-2. The data collected from this study will serve the purpose of confirming safety and performance of the Avenir Müller Hip Stem.

Completed8 enrollment criteria

AESCULAP® Plasmafit® Cementless Acetabular System With Vitelene® Vitamin E Stabilized Highly Crosslinked...

OsteoarthritisHip2 more

Objectives of this study is evaluate effectivness of AESCULAP® Plasmafit® Plasmafit Cementless Acetabular System With Vitelene® Vitamin E Stabilized Highly Crosslinked Polyethylene compare to the sane sistem without Vitamin E, and ceramic or metal femoral heads

Completed3 enrollment criteria

A Prospective, Randomized Trial Comparing Same Day Discharge and Overnight Hospital Stay Among Total...

Osteoarthritis of the Hip

The purpose of this study is to identify differences in satisfaction, pain and length of stay between patients undergoing hip replacement who are discharged from the hospital on the day of surgery compared to patients who stay one night in the hospital.

Completed24 enrollment criteria

Etude 3000 ARTHROSES Symptomatic Knee and Hip Osteoarthritis Prevalence Survey

Osteoarthritis

Nationwide descriptive epidemiology survey aiming to determine lower limb OA prevalence, based on a validated method previously used to assess inflammatory rheumatism (rheumatoid arthritis and spondylarthropathy) prevalence in France.

Completed2 enrollment criteria

Safety and Efficacy of the SL PLUS and the SL PLUS MIA Hip Stem

Coxarthrosis

Randomized controlled trial using two types of hip stems, SL PLUS MIA (control group) and SL PLUS (study group). We compare primary and secondary stability of both hip stems for radiographic outcome using EBRA (Ein-Bild-Roentgen-Analyse) after a two year follow-up period. Further, we compare all differences in clinical outcome using Harris Hip Score, Oxford hip score and radiographic findings.

Completed10 enrollment criteria

Comparison of Knotless Barbed Suture and Standard Suture in Knee Replacement Patients

Knee OsteoarthritisHip Osteoarthritis

Barbed suture use has been gaining increased acceptance and has been reported to offer potential advantages in wound closure of hip and knee replacement surgeries. The goal of this study is to compare joint replacement patient outcomes who receive a knotless barbed suture versus a traditional suture (randomized into two arms). The traditional suture used at our joint replacement program is defined as: interrupted sutures to close the retinaculum followed by running monocryl sutures for skin closure. Both knotless barbed suture and the traditional sutures have similar suture size. Patient outcomes examined will be patient range of motion (recorded daily) and complications with wound healing (evaluated periodically in-person at post-operative visits). Secondary outcomes examined will include wound drainage on dressings by surface area and weight, as well as the wound cosmesis and perceived presence of subcutaneous surgical knots.

Completed3 enrollment criteria
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