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Joint Diseases clinical trials

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NCT ID: NCT04026074 Completed - Knee Arthropathy Clinical Trials

Concepts for Analgosedation During Placement of Regional Anaesthesia Before Operations.

Start date: July 26, 2019
Phase: Phase 4
Study type: Interventional

Aim of the study is to specify the best analgosedation technique during placement of regional anaesthesia from the patients' view. In this double blind randomized trial the investigators will be testing the application of drugs administered intravenously (fentanyl-bolus, remifentanil-infusion, clonidine-bolus) or transcutaneously (EMLA salve) or placebo (NaCl 0,9% i.v. and skin protection salve).

NCT ID: NCT04024176 Completed - Arthropathy Clinical Trials

Gait Analysis in Moderate Hemophiliac Patients (AQM-Hemophile)

Start date: November 29, 2019
Phase: N/A
Study type: Interventional

The management of moderate hemophilia is less codified than those of severe patients; because these patients are theoretically less likely to bleed and therefore less likely to develop arthropathies. Nowaways, the question arises as to the appropriateness of this "symptomatic" management for the prevention of the occurrence of hemophilic arthropathies. Indeed, a significant number of moderate hemophiliacs seems to develop severe arthropathies that cause significant disability. However, because of the very small proportion of these patients in the total number of hemophiliacs, data are lacking on the impact of arthropathies on this population. The investigators therefore propose to include moderate hemophiliac patients in the study to carry out an evaluation of gait, using a gait analysis to determine the consequences of arthropathies, even sub-clinical ones, according to the duration of the disease's progression. In an associated way, the analysis of different clinical (joint assessment; quality of life score;...), radiological (radiographic; ultrasound (synovial thickness)), biological (level of associated factors ; other associated marker), in order to provide a complete picture of the articular situation in these patients with moderate haemophilia.

NCT ID: NCT04019093 Completed - Clinical trials for Temporomandibular Joint Disorders

Acute Effects of Alcohol Use on Chronic Orofacial Pain

Start date: November 5, 2019
Phase: N/A
Study type: Interventional

Self-medication of pain with alcohol is a common, yet risky, behavior among individuals with chronic orofacial pain. Chronic pain status may affect the degree to which alcohol use relieves pain, but the independent contributions of pain chronification and alcohol-related expectations and conditioning have not been previously studied. This project addresses this gap in knowledge and will inform further research and clinical/translational efforts for reducing risk associated with these behaviors.

NCT ID: NCT04010916 Completed - Knee Arthropathy Clinical Trials

The Efficacy Of Ultrasound-Guided Adductor Canal Block for Arthroscopic Knee Surgery

Start date: July 1, 2019
Phase: N/A
Study type: Interventional

The ultrasound-guided selective blockade of the saphenous nerve in the adductor canal provides effective analgesia and reduces postoperative pain in patients undergoing arthroscopic medial meniscectomy. Selective blockade of the saphenous nerve in the adductor canal provides effective analgesia without quadriceps muscle weakness. It has been shown that usage of tourniquet during performing the adductor canal block (ACB) block increases the spread of local anesthetics in a distal and proximal way. Therefore, the proximal spread of local anesthetics may cause possible quadriceps weakness. The distal spread of local anesthetics may increase analgesic effect via sciatic nerve. The timing of the tourniquet inflation for ACB is a topic of discussion.The aim of this study is to compare the different times of US-guided ACB performing for postoperative analgesia management after arthroscopic knee surgery.

NCT ID: NCT04004429 Completed - Clinical trials for Rheumatoid Arthritis

A Study of the Safety, Tolerability and Efficacy of Treatment With AP1189 in Early RA Patients With Active Joint Disease

SynAct-CS002
Start date: August 26, 2019
Phase: Phase 2
Study type: Interventional

This is a multicenter, two-part, randomized, double-blind, placebo-kontrolled, 4-week study with repeated doses of AP1189. The study population will consist of newly diagnosed subjects with severe active Rheumatoid Arthritis, defined with a Clinical Disease Activity score (CDAI) > 22, who are to start up-titration with methotrexate.

NCT ID: NCT03977454 Completed - Hip Arthropathy Clinical Trials

Periarticular Injection Versus Peripheral Nerve Block in Total Hip Arthroplasty

Start date: November 11, 2019
Phase: Phase 2
Study type: Interventional

This study will assess if preoperative quadratus lumborum block (QLB)/lateral femoral cutaneous nerve block (LFCNB) with ropivacaine and glucocorticoids provide more effective analgesia than periarticular injection (PAI) with the same mixture in total hip arthroplasty (THA).

NCT ID: NCT03965507 Completed - Clinical trials for Lumbar Disc Herniation

The Prevalence Of Sacroiliac Joint Dysfunction In Patients With Lumbar Disc Hernia

Start date: January 22, 2015
Phase:
Study type: Observational

In this study evaluated the prevalence of sacroiliac joint dysfunction in patients with lumbar disc hernia and examined the variations in clinical parameters cause by this combination.

NCT ID: NCT03954912 Completed - Clinical trials for Osteoarthritis, Knee

Comparative Outcomes Between Image-based Versus Imageless Robot-assisted Unicondylar Knee Arthroplasty

Start date: June 1, 2015
Phase: N/A
Study type: Interventional

This prospective cohort study was conducted with the aim of comparing relevant clinical outcomes which included intra (surgical time and blood loss), post-operative outcomes (range of motion, function, complications and revisions) and return to activity between imageless and image-based surgical system in medial unicondylar knee arthroplasty

NCT ID: NCT03942939 Completed - Knee Arthropathy Clinical Trials

Tourniquet vs. Short Time Tourniquet in Primary Robotic Assisted TKA

Start date: August 27, 2019
Phase: N/A
Study type: Interventional

The goal of this prospective, randomized study is to compare the outcomes of patients undergoing Robotic Arm-Assisted TKA (RA-TKA) with the intraoperative use of a tourniquet to those undergoing RA-TKA with a short tourniquet time.

NCT ID: NCT03921034 Completed - Anesthesia Clinical Trials

IPACK Nerve Block for Total Knee Arthroplasty

Start date: November 17, 2016
Phase: Phase 4
Study type: Interventional

Double-blind, randomized controlled clinical trial to test the efficacy of IPACK on postoperative opioid consumption, patient satisfaction, pain scores, mobility, and several other secondary outcomes in adults undergoing primary unilateral TKA. Enrolled patients will be randomized to either continuous ACB with IPACK or to continuous ACB with sham subcutaneous saline injection. Outcomes assessors and patients will be blinded to the intervention.