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Knee Replacement, Total clinical trials

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NCT ID: NCT05490186 Recruiting - Pain, Postoperative Clinical Trials

Function, Pain, and Alignment Following Knee Replacement for the Treatment of Osteoarthritis

Start date: November 16, 2021
Phase: N/A
Study type: Interventional

There are many factors that can influence patient satisfaction and patient related outcomes following total knee replacement including the surgical alignment of the joint components. Historically, total knee replacements have been performed with an aim aiming to achieve neutral alignment or a mechanical weight axis in the lower extremity . However, only 0.1 % of the population have a pre-surgical anatomical neutral alignment, and therefore the constitutional anatomy of the patient is neglected. There is a growing trend to return patients back their anatomical constitutional alignment after a knee replacement, referred to as Kinematic Alignment using robotics. The aim of this randomized controlled trial is to examine how mechanical alignment and kinematic alignment impacts function, pain, mood and fatigue following TKR for the treatment of osteoarthritis. Outcomes will be measured at 6 week, 6 months, 1 year and 2 years after surgery.

NCT ID: NCT04286035 Completed - Pain, Postoperative Clinical Trials

Two Different Blocks for Postoperative Analgesia in Patients Undergoing Unilateral Total Knee Arthroplasty

Start date: April 2, 2019
Phase: Phase 4
Study type: Interventional

The frequency of femoral nerve block and adductor canal block for analgesia after TKA(total knee arthroplasty) increases with the use of ultrasonography in regional anesthesia. In this study, we aimed to compare the effects of femoral nerve block and adductor canal block on postoperative analgesia in patients undergoing unilateral knee arthroplasty.

NCT ID: NCT04090125 Completed - Clinical trials for Knee Arthroplasty, Total

Improving Physical Activity and Gait Symmetry After Total Knee Arthroplasty

PAS-TKA
Start date: November 8, 2019
Phase: N/A
Study type: Interventional

The purpose of this pilot study is to examine the effectiveness of the Physical Activity and Symmetry (PAS) program, compared to an attention (ATT)control group, for patients with post-total knee arthroplasty (TKA). The investigators hypothesize that the PAS treatment will result in meaningful improvements in physical activity (PA) and joint loading symmetry compared to the ATT group.

NCT ID: NCT03492320 Completed - Clinical trials for Total Knee Replacement

Progression of Health Related Quality of Life of Patients Waiting for Total Knee Arthroplasty

TKA HRQoL
Start date: March 1, 2013
Phase:
Study type: Observational

To evaluate the progression on patients suffering from end stage OA whilst being on the waiting list for TKR

NCT ID: NCT02830087 Terminated - Clinical trials for Knee Arthroplasty, Total

Tourniquet Pressure in Primary Total Knee Arthroplasty

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

This proposed novel randomized control trial (RCT) seeks to address this gap in TKA protocol by gaining a better understanding of the relationship between tourniquet pressure and time, and intraoperative performance and post-operative outcomes. This study does not seek to answer the question of "tourniquet vs no tourniquet", but to seek a tourniquet usage that would maximize the intraoperative benefits for the surgeon and minimize the negative consequences for patient outcomes. Specific Aim #1: enroll around 146 primary TKA patients. Specific Aim #2: evaluate different tourniquet cuff pressures (TCP) and tourniquet times in relation to intraoperative performance. Specific Aim #3: evaluate different TCP and tourniquet times in relation to post-operative pain and complications of short-term, intermediate, and long-term followup. Specific Aim #4: evaluate different TCP and tourniquet times in relation to post-operative function of short-term, intermediate, and long-term followup.

NCT ID: NCT02474654 Completed - Clinical trials for Knee Replacement, Total

Implementation of a Pain Management Protocol for Total Knee Arthroplasty

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

Study question: Is there an ideal combination of intraoperative long acting analgesics (periarticular infiltration (PI), femoral nerve block (FB) and intrathecal opioids (IO)) to optimize post-operative functional recovery, decrease overall narcotic consumption and enable faster 'readiness to discharge' for patients undergoing primary total knee replacement (TKR)?