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Knee Discomfort clinical trials

View clinical trials related to Knee Discomfort.

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NCT ID: NCT06277401 Recruiting - Knee Discomfort Clinical Trials

Exercise in Patients With Hypermobile Joints and Knee Pain

HIPEr-Knee
Start date: February 21, 2024
Phase: N/A
Study type: Interventional

Pain associated with knee joint hypermobility is common in the adult population, but evidence on treatment is sparse. This study investigates if high-load resistance training is superior to usual care in improving activity-related pain in young patients (18-45 years) with hypermobile joints and knee pain.

NCT ID: NCT05975879 Completed - Osteoarthritis Clinical Trials

A Study of the Feasibility of Using the Dietary Supplement "ARTNEO" in Patients With Osteoathritis

Start date: May 31, 2022
Phase: N/A
Study type: Interventional

The goal of this clinical study is to evaluate the effectiveness of the properties that support the functional state of the joints and the safety of the dietary supplement for food ARTNEO®, oral capsules, in patients with stage II-III primary osteoarthritis of the knee joint. The main questions it aims to answer are: 1. To evaluate the effectiveness of the joint functional state-supporting properties of dietary supplement ARTNEO®, capsules for oral administration, in patients with stage II-III primary osteoarthritis of the knee joint; 2. To evaluate the safety of dietary supplement ARTNEO®, capsules for oral administration, in patients with stage II-III primary osteoarthritis of the knee joint. Participants will be randomly distributed equally among two groups: - Group 1 "ARTNEO" (106 people): patients take the study dietary supplement ARTNEO®, 1 capsule 1 time per day for 6 months; - Group 2 "Placebo" (106 people): patients take placebo 1 capsule 1 time per day for 6 months.

NCT ID: NCT05824676 Not yet recruiting - Trauma Clinical Trials

DePuy Synthes Variable Angle LCP Patella Plating System Study

Start date: May 2023
Phase: N/A
Study type: Interventional

The Depuy Synthes Locking Compression Plate (LCP) Variable Angle Patella Plating System is an FDA approved device. The purpose of this study is to see how well the Depuy Synthes LCP Variable Plating System work in fixing a broken kneecap (patella). Depuy says that the device will improve healing when compared to traditional ways of repairing a broken patella. The goal of this randomized control trial is to learn how well the LCP Variable Plating System works to fix a broken patella (kneecap) compared to traditional fixation methods, in male and females, age 18 to 74, with a patellar fracture, and being treated at Hartford HealthCare The Bone and Joint Institute or Hartford Hospital. The main question it aims to answer are: - To understand if the Depuy Synthes LCP Variable Angle Plating System will provide a better way to help patients recover from a broken patella. Participants will evaluated at specific time points: post-op day 1, 6 weeks, 3 months, 6 months, and 12 month post-surgery. Participants will be asked to: - Complete surveys at all evaluation timepoints. - Have x-rays(radiographs) taken at the 6 week, 3 month, 6 month, 9 month, and 1 year timepoints. - Participants will have a passive range of motion tests done at 6 week, 3 month, 6 month, 9 month, and 1 year timepoints. - Participants would have strength and balance tests done at the 3 month, 6 month, 9 month, and 1 year timepoints.

NCT ID: NCT05822401 Not yet recruiting - Knee Osteoarthritis Clinical Trials

Prevention, Management and Rehabilitation of Knee Osteoarthritis at the Workplace

Start date: April 11, 2023
Phase: N/A
Study type: Interventional

The goal of this intervention study is to assess the effect of blood flow restricted (BFR) exercise integrated into the daily work tasks among hospital workers with or at increased risk of chronic knee pain. The main questions are: Can BFR exercise integrated into the daily work tasks reduce knee pain (primary outcome) and improve function and work ability among hospital workers with or at increased risk of chronic knee pain? Participants in the intervention group will for shorts bouts during their workdays integrate BFR into their daily work tasks involving walking, whereas the control group will continue as usual.

NCT ID: NCT05347602 Completed - Clinical trials for Rheumatoid Arthritis

Gold Factor on Knee Joint Health and Function

Start date: August 3, 2020
Phase: N/A
Study type: Interventional

The purpose of this clinical study was to determine whether gold nanoparticles (AuNP) supplement holds clinical value in improving joint health, function, and quality of life for arthritis patients.

NCT ID: NCT05060536 Recruiting - Clinical trials for Arthroplasty Complications

Infrapatellar Fat Pad Excision in Total Knee Arthroplasty

Start date: August 31, 2021
Phase: N/A
Study type: Interventional

To examine whether removing the infrapatellar fat pad from the knee during total knee arthroplasty affects the patient outcome in terms of pain and knee function following the procedure. Currently there is no consensus on whether removing this tissue from the knee has a positive or detrimental effect. Small studies have been published, some showing improved symptoms and some worse symptoms. Current practice of orthopaedic surgeons is either to routinely remove or routinely retain the tissue when performing total knee arthroplasty.

NCT ID: NCT04752761 Recruiting - Knee Discomfort Clinical Trials

Compliance With PROMs Detection Through Digital Support and Correlation Compared Standard to Outpatient Detection in Knee Prosthetics

DIG-PROMs-k
Start date: November 30, 2020
Phase: N/A
Study type: Interventional

Two methods for detecting outcomes after knee prosthetic surgery are compared: the traditional one using paper questionnaires administered in the outpatient setting (Oxford Knee Score) VS detection using digital questionnaires created on Google Forms and sent to the patient's smartphone on which the compilation takes place in the extra area outpatient.

NCT ID: NCT04537013 Recruiting - Knee Injuries Clinical Trials

Clinical Study of Chondro-Gide® for Large Chondral Lesions in the Knee

SECURE
Start date: August 26, 2020
Phase: N/A
Study type: Interventional

Multi-center, prospective, concurrently controlled, non-randomized, double-blind (patient and assessor). Treatment of large chondral lesions in the knee with microfracture plus the Chondro-Gide® ACC is non-inferior to treatment of small chondral lesions treated with microfracture alone.

NCT ID: NCT04506411 Completed - Joint Pain Clinical Trials

Turmeric Efficacy for Mobility and Joint Function

T-MOTION
Start date: September 24, 2020
Phase: N/A
Study type: Interventional

The objective of the study is to test the capacity of a 12-weeks Turmipure GOLD® supplementation to reduce joint discomfort.

NCT ID: NCT04420091 Completed - Knee Discomfort Clinical Trials

Hydrolyzed Fish Cartilage Effect on Knee Joint Functionality and Discomfort in Adult Population

Start date: June 11, 2020
Phase: N/A
Study type: Interventional

This study is an exploratory, non-comparative, multi-centric trial in 30 free-living healthy male and female subjects with moderate knee joint discomfort and loss of functionality. The objective of this trial is to determine whether oral administration of Cartidyss, a concentrated fish cartilage extract, can contribute to the improvement of knee joint functionality and discomfort in adult population