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Tibial Plateau Fracture clinical trials

View clinical trials related to Tibial Plateau Fracture.

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NCT ID: NCT05571449 Recruiting - Clinical trials for Tibial Plateau Fracture

Efficacy of the Use of 3D Printing Models in the Treatment of Tibial Plateau Fractures: a Randomized Clinical Trial

Start date: October 1, 2022
Phase: N/A
Study type: Interventional

TIBIA3D is a randomized, open and prospective clinical trail that evaluates the use of preoperative 3D printing in the surgical treatment of patients with tibial plateau fractures

NCT ID: NCT05521958 Enrolling by invitation - Clinical trials for Tibial Plateau Fracture

Gene Expression in Lower Extremity Acute Traumatic Compartment Syndrome

Start date: June 10, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate both genotypic differences and differences in local gene expression in individuals who develop acute traumatic compartment syndrome relative to control patients with at-risk lower extremity fractures who do not develop compartment syndrome.

NCT ID: NCT05397327 Not yet recruiting - Clinical trials for Tibial Plateau Fracture

3D Virtual Planning for Tibial Plateau Fractures

Start date: June 1, 2022
Phase: N/A
Study type: Interventional

Tibial plateau fractures are often complex fractures and need a good preoperative planning. The investigators think that a 3D virtual planning software will help the surgeons to get a better understanding of the fracture and therefore want to study the value of 3D virtual planning software in the preoperative planning of tibial plateau fractures. The investigators hypothesize that this software will shorten the duration of surgery, decrease the peroperative bloodloss and the number of complications. Patients with tibial plateau fractures who need surgical treatment will be asked to participate in this study. After participants have given informed consent, they will be randomized between a 'traditional preoperative planning' and a '3D virtual preoperative planning' group. Surgeons will plan their surgery using traditional planning tools (X-rays and CT scan) or traditional planning tools ánd the 3D virtual planning software. 6 weeks, 3 months and 6 months after surgery, participants will be asked to fill in 2 questionnaires about knee pain and knee function. After surgery a CT scan or X-ray will be performed conform standard of care in the hospital.

NCT ID: NCT04983316 Recruiting - Clinical trials for Tibial Plateau Fracture

TPF Machine Learning Algorithms

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

To adopt a machine learning technique to decide whether operative or non-operative treatment will result in the best patient-outcome.

NCT ID: NCT04639011 Withdrawn - Pain, Postoperative Clinical Trials

Duloxetine Tibial Plateau

Start date: October 2022
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if Duloxetine provides effective pain management for adult patients (18 or older) undergoing tibial plateau surgery. Participants from two institutions will be randomized to one of two treatment groups: control (Group A) and treatment (Group B). Group A control group will receive placebo of sugar pill and BMC standard of care - namely postoperative, IV administration of opioids via a patient controlled analgesia (PCA) system which utilizes a hydromorphone pump (BMC standard of care). Group B, the intervention group, will receive three doses of 60 mg of oral duloxetine (right before operation, postop day 1, postop day 2). This study is important as tibial plateau surgery's postoperative pain management primarily involved providing opioids, and if duloxetine can result in reduced narcotic intake and lower pain scores, it can potentially improve patient care, rehabilitation, early movement, and shorter length of hospital stay.

NCT ID: NCT04314570 Not yet recruiting - Pain, Postoperative Clinical Trials

Saphenous Nerve Block After Tibial Plateau ORIF

Start date: May 2025
Phase: N/A
Study type: Interventional

Fractures of the tibial plateau, while very painful, typically do not receive nerve blocks. This is because of a concern that the numbness from a nerve block would "mask" the typically painful symptoms of compartment syndrome, a condition that can lead to a permanent loss of function of the injured limb. Our study aims to evaluate the effectiveness of saphenous nerve block for pain management after surgical repair of a tibial plateau fracture. Based on cadaver studies and our clinical experience, we suspect that the saphenous nerve contributes to pain sensations of the tibial plateau and will not mask the pain from a compartment syndrome. In summary, while saphenous nerve block represents a safe option after tibial plateau open reduction internal fixation (ORIF), we aim to evaluate its effectiveness in this patient population.

NCT ID: NCT03562364 Completed - Clinical trials for Distal Femur Fracture

Early Advanced Weight Bearing for Peri-articular Knee and Pilon Injuries

AlterG
Start date: February 25, 2019
Phase: N/A
Study type: Interventional

The overall objective of this study is to compare outcomes following early advanced weight bearing (EAWB) using the AlterG antigravity treadmill versus standard of care physical therapy for adult patients with lower extremity periarticular injuries.

NCT ID: NCT02168959 Completed - Clinical trials for Tibial Plateau Fracture

Continuous Femoral Nerve Block With a Tibial Plateau Fracture

Start date: February 2013
Phase: Phase 0
Study type: Interventional

The primary purpose of the proposed study is to compare postoperative pain scores and total opioid consumption between two groups randomized to either receive or not receive a femoral nerve block for pain control following surgical repair of a tibial plateau fracture. Pain will be assessed post-operatively using standard numeric pain scores rated on a 0 - 10 scale, as well as using the University new pain assessment tool - the Clinically Aligned Pain Assessment (CAPA). This new 5 question pain assessment tool has not yet been validated, but does address several key questions, including patient comfort, pain control, change in pain status, daily functioning, and sleep quality. Along with post-operative pain scores, we will compare total opioid consumption between the two groups. The null hypothesis is that there is no difference in pain scores or total opioid consumption between patients receiving a femoral nerve block and those without a nerve block following surgical repair of a tibial plateau fracture. A secondary outcome will examine long-term pain control, range of motion, and functional status of these patients at their regular orthopedic clinic follow-up appointments. The same pain scores will be assessed, along with quadriceps strength and knee range of motion. Patients will complete the PROMIS Physical Function CAT and short Musculoskeletal Function Assessment, patient reported outcomes tools to evalute physical function. A teriary outcome will be to retrospectively examine postoperative pain scores and total opioid consumption for all tibial plateau fracture patients seen at the University of Utah for surgical repair in the past 10 years.