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Arthroplasty, Replacement, Hip clinical trials

View clinical trials related to Arthroplasty, Replacement, Hip.

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NCT ID: NCT05666479 Active, not recruiting - Clinical trials for Diabetes Mellitus, Type 2

CGM Monitoring in T2DM Patients Undergoing Orthopaedic Replacement Surgery

Start date: September 9, 2022
Phase:
Study type: Observational

The purpose of this study is to analyze the efficacy and accuracy of real-time continuous glucose monitoring devices (rtCGM) in patients with Type 2 diabetes undergoing inpatient elective hip or knee surgery in the pre-, peri-, and post-operative setting at Stony Brook University Hospital (SBUH).

NCT ID: NCT05075200 Active, not recruiting - Clinical trials for Arthroplasty, Replacement, Knee

Tranexamic Acid Dosing for Major Joint Replacement Surgery

TXA-Dosing
Start date: December 14, 2021
Phase: Phase 2
Study type: Interventional

Over 1.7 million hip and knee replacements are performed every year worldwide. These surgeries are associated with high blood loss and transfusion rates. In older patients, the high blood loss can result in postoperative anemia. Anemia is a condition where there is a lack of healthy red blood cells to carry oxygen around the body. This means, the patient may need a blood transfusion. This can result in different immune responses such as lung injury, fluid overload, and sepsis. The purpose of this study is to find an optimal dose of tranexamic acid (TXA) to be given during a hip or knee replacement surgery. TXA is one of the drugs given during surgery because it lowers the amount of bleeding and the risk of a blood transfusion. Individuals who are chosen to participate in the study will be split into two separate groups. After anesthesia is administered, study participant will be given the hospitals standard dose of TXA which is 20mg/kg. However, in patients with kidney problems and lower kidney functions, the dose will be lowered because TXA is filtered out of the body through the kidneys. Throughout the surgery and after it, patients will have about 30-50mL (3-5 tablespoons) of blood samples drawn at specific time points. This will be done through IV line which will stay in place during the surgery and post operation to minimize the amount of needle puncturing's. This study will help to development a new dosing guideline for TXA in patients who are undergoing joint replacement surgery.

NCT ID: NCT04831372 Active, not recruiting - Osteoarthritis, Hip Clinical Trials

On-Table Versus Off-Table Total Hip Arthroplasty

Start date: April 7, 2021
Phase: N/A
Study type: Interventional

The Direct Anterior Approach (DAA) is a common way to perform total hip arthroplasty. There are two main techniques to perform total hip replacement through the anterior approach. The first method is the "on-table" method, which uses a specialized surgical table, called a traction table. This table involves placing both feet in specialized boots that are then hooked up to the table, and allows for positioning of the operative leg with aid of the table. The major limitations associated with the traction table are the need for two additional staff members and the purchase of said table. The second method is the "off-table" method. In this method the patient is placed on a standard operating room table and the operative leg is manually positioned by the surgeon during the procedure . This obviates the need for the additional staff members or purchase of a specialized table. Both the "on-table" and "off-table" techniques are routinely used both worldwide and by our joint replacement specialists at Carilion Clinic. This study will aim to compare the efficiency and efficacy of performing the DAA for total hip arthroplasty utilizing either the "on-table" or "off- table" technique. Patients will be randomized to receive their total hip arthroplasty with either the "on- table" or "off-table" method.

NCT ID: NCT03274830 Active, not recruiting - Clinical trials for Arthroplasty, Replacement, Hip

A Post Market Clinical Follow-up Study With the aneXys Cup

Start date: March 5, 2020
Phase:
Study type: Observational

The purpose of the study is the evaluation of the clinical and radiological short- to long-term safety and performance of the aneXys cup. The data will be used for an ongoing evaluation of the product safety and performance.

NCT ID: NCT02999009 Active, not recruiting - Clinical trials for Arthroplasty, Replacement, Hip

Trident II Tritanium Acetabular Shell Outcomes Study

Start date: January 20, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to review the performance and success rate of an FDA approved cementless hip replacement part called the Trident II Tritanium Acetabular Shell. The study will specifically look at the need to revise the hip replacement after 5 years. This will be compared to how much this happens in patients who have hip replacement with similar cementless acetabular shells.

NCT ID: NCT02520544 Active, not recruiting - Clinical trials for Arthroplasty, Replacement, Hip

ATX Register Accolade Stem & Trident/Tritanium Cup With X3 Insert

ATX
Start date: January 2012
Phase: N/A
Study type: Interventional

The aim of this register is to determine the Accolade/Accolade II stem and Trident/Tritanium cup survivorship over years.

NCT ID: NCT02385409 Active, not recruiting - Anemia Clinical Trials

Incidence and Reasons for Preoperative Anemia in Elective Lower Joint Arthroplasty

Start date: May 2013
Phase: N/A
Study type: Observational

Preoperative anemia is an independent risk factor for the need for allogeneic transfusion during surgery and increased postoperative morbidity. Treatment of preoperative anemia is recommended. However the type of preoperative anemias in elective hip- and knee surgery has only been sparsely studied. This observational study aims to investigate the incidence and type of anemias prior to elective hip- and knee arthroplasty.

NCT ID: NCT02371382 Active, not recruiting - Clinical trials for Arthroplasty, Replacement, Hip

Multicentre Prospective Study to Evaluate Long-term Clinical Outcomes of the Sirius Cemented Femoral Stem

Sirius
Start date: March 2013
Phase:
Study type: Observational

The purpose of this multicentre, prospective study is: - Document the Clinical and Radiographic performance of the stem at 3 months, 1 year, 3 years, 5 years, 7 and 10 years. - Report Safety and Survivorship up to 10 years F/up.

NCT ID: NCT01917929 Active, not recruiting - Clinical trials for Arthroplasty, Replacement, Hip

Secur-Fit Advanced Outcomes Study

Start date: August 1, 2013
Phase: N/A
Study type: Interventional

This study is a prospective, open-label, post-market, non-randomized, multi-center clinical evaluation of the Secur-Fit Advanced Hip Stem for primary total hip arthroplasty with a cementless application in a consecutive series of patients who meet the eligibility criteria. The success rate of the Secur-Fit Advanced femoral stem, defined as absence of stem revision for aseptic loosening or femoral fracture, is expected to be no worse than 99% at 5 years postoperative with a non-inferiority margin of 2.5%.

NCT ID: NCT01878175 Active, not recruiting - Clinical trials for Arthroplasty, Replacement, Hip

Functional Movement Retraining After Hip Replacement

FMR-THA
Start date: May 2014
Phase: N/A
Study type: Interventional

Total hip arthroplasty (THA) is a common surgical procedure among Veterans. It is most often used to treat hip osteoarthritis, which is more common among Veterans than the general population. Some patients continue to experience functional limitations after THA, and studies have shown that these patients still tend to put greater loads on the opposite leg, which can increase the risk of developing osteoarthritis in that leg. One likely reason for these post-surgical limitations is that rehabilitation is very minimal following this procedure. This project will involve development and preliminary testing of a functional movement retraining program, designed to help Veterans improve their function and biomechanics after THA. The project will also develop processes for delivering this program in Veterans' homes, to increase accessibility.