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Hip Arthroplasty clinical trials

View clinical trials related to Hip Arthroplasty.

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NCT ID: NCT02207296 Completed - General Anesthesia Clinical Trials

Operative Hemodynamic Optimization Using the Plethysmographic Variability Index During Orthopedic Surgery

OPVI
Start date: February 2015
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether an operative hemodynamic optimization using the plethysmographic variability index during orthopedic surgery could decrease the length of hospital stay and the postoperative morbidity.

NCT ID: NCT01520961 Completed - Clinical trials for Femoral Neck Fractures

Functional Recovery After Partial Hip Arthroplasty: Anterior or Posterolateral Approach?

AYNF
Start date: January 2012
Phase: N/A
Study type: Observational

Hueter anterior approach as described by Siguier allows an anatomical approach without muscle or tendon sections. It minimizes the rate of dislocation after primary total hip arthroplasty (1.5%, Sariali)and seems to allow quicker rehabilitation. The investigators hypothesis was Hueter anterior approach allows quicker functional recovery after partial hip replacement.

NCT ID: NCT01382927 Recruiting - Obesity Clinical Trials

Impact of Spontaneous Breathing on Ventilation Distribution in Obese Patients

Start date: April 2011
Phase: N/A
Study type: Observational

General anesthesia (GA) and paralysis are factors which facilitate atelectasis formation, especially in obese patients. Spontaneous breathing can reduce the amount of atelectasis. In this study, the investigators are comaparing obese patients undergoing hip arthroplasty in GA versus spinal anesthesia. Distribution of ventilation during and after anesthesia is assessed by eletrical impedance tomography (EIT).

NCT ID: NCT01366911 Completed - Hip Arthroplasty Clinical Trials

Stem Cells Predicting Orthopedic Outcomes

Start date: April 22, 2011
Phase:
Study type: Observational

This is a pilot study to provide preliminary data of the association between bone mineral denity adjacent to acetabular implants, as measured by quanitative computed tomography (QCT), at least 2 years post Total Hip Arthoplasty (THA) surgery with Mesechymal stem cell assays, obtained at time of surgery, and to begin to evaluate if stem cells can predict orthopaedic surgical outcomes.

NCT ID: NCT01349179 Completed - Hip Arthroplasty Clinical Trials

Scan Hip Evaluation

ETOSA
Start date: December 2010
Phase: N/A
Study type: Interventional

The couple of friction metal-polyethylene is regarded as the couple of reference in spite of the osteolysis induced by the wear of the polyethylene which remains the independent factor of long-term failure. This is all the more true as the patients are young, thus justifying the recourse to alternate couples of friction. The Metasul® couple was introduced on the French market under its current form in 1995 (year of its marking EC). The use of a couple of friction metal-metal (MM) is justified because it would be likely to improve longevity of the total arthroplasties of the active subjects by the reduction in osteolysis related to the wear of polyethylene. Various studies highlight evolutions different according to the types of fixing acetabular; favourable results of the not cemented cups contrasting with unsealings and the evolutionary edgings of the Metasul® cups cemented of or the cups "of cemented Weber type".

NCT ID: NCT01017562 Completed - Hip Arthroplasty Clinical Trials

Differentiation of Aseptic From Septic Loosening by 18F-fluoride PET

Start date: April 2007
Phase: N/A
Study type: Observational

In this study, the investigators utilized the 18F-fluoride PET method to evaluate THA cases with a stable, septic or septic loosened implant in order to differentiate these clinical settings using a novel uptake type classification approach.

NCT ID: NCT00967980 Completed - Hip Arthroplasty Clinical Trials

Femoral Versus Psoas Continuous Peripheral Nerve Blocks Following Hip Arthroplasty

Start date: September 2009
Phase: Phase 4
Study type: Interventional

The purpose of this research study is to determine if the insertion site of a perineural catheter, or tiny tube placed next to the nerves that go to the hip which you will have surgery, affects the amount of pain relief that is experienced after surgery.

NCT ID: NCT00934661 Terminated - Hip Arthroplasty Clinical Trials

Low Dose Extended-release Epidural and Lumbar Plexus Block Compared to Lumbar Plexus Block for Total Hip Resurfacing

Start date: January 2010
Phase: Phase 4
Study type: Interventional

At Wake Forest University, the investigators have been using Extended Release Epidural Morphine (EREM), since late 2004, as part of multimodal analgesia in patients having gynecologic surgeries and hip arthroplasties. Hypothesis: In patients undergoing a Birmingham total hip arthroplasty (BHA), low dose EREM in conjunction with lumbar plexus block (LPB) will be better than lumbar plexus block alone in increasing proportion of patients who meet discharge criteria within 24 hours.

NCT ID: NCT00921908 Completed - Postoperative Pain Clinical Trials

Multihole or Epidural Catheter for Local Anesthetic in the Wound

Start date: October 2008
Phase: N/A
Study type: Observational

Postoperative administration of local anesthetics is effective for postoperative pain management across surgical specialties but the optimal type of catheter (single, few or multiholed catheters) has not been determined. This study investigates wound spread of a radioactive isotope (technetium) administered in different types of catheters after total hip arthroplasty.

NCT ID: NCT00912873 Completed - Hip Arthroplasty Clinical Trials

Optimizing Local Anesthetic Concentration for Continuous Lumbar Plexus Nerve Blocks

Start date: May 2008
Phase: Phase 4
Study type: Interventional

This is a research study to determine if the concentration of local anesthetic through a catheter next to the nerves that go to the hip that is undergoing surgery, affects muscle strength and sense of touch experienced after surgery. This study is looking at the varying concentrations of local anesthetic placed through the catheter.