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NCT ID: NCT05828433 Completed - Clinical trials for Benign Paroxysmal Positional Vertigo

Effect of Epley-Canalith Repositioning Procedure and Vestibular Rehabilitation Therapy in Diabetic Patients With BPPV

Start date: January 7, 2022
Phase: N/A
Study type: Interventional

Benign paroxysmal positional vertigo (BPPV) is a common inner ear disorder characterized by brief episodes of vertigo caused by changes in head position. The condition can cause significant func-tional impairment and reduced quality of life. BPPV is especially common among diabetic patients. The Epley-Canalith Repositioning Procedure (CRP) and Vestibular Rehabilitation Therapy (VRT) are two commonly used interventions for the treatment of BPPV. The objective of this paper is to determine the effective therapy among Epley-Canalith Repositioning Procedure and Vestibular Rehabilitation for improving balance and posture control in Diabetic patients with Benign Parox-ysmal Positional Vertigo. Thirty subjects with Diabetes Mellitus (Type 2) suffering from Benign Paroxysmal Positional Vertigo (BPPV) were recruited for the study and randomly assigned to groups A and B, underwent Canalith Repositioning Procedure and Vestibular Rehabilitation Therapy respectively. The outcome measures of the study were Vertigo Symptom Scale- Short Form (VSS-sf) score and Berg Balance Scale Form (BBS) score assessed at pre -treatment (pre) and 4 weeks post treatment (post).

NCT ID: NCT05827263 Completed - Clinical trials for Temporomandibular Joint Disorders

Temporary Hydrostatic Splint Therapy and Its Effects on Occlusal Forces

Start date: December 1, 2021
Phase: N/A
Study type: Interventional

The goal of this non-randomized controlled trial is to analyze and compare occlusal force distribution patterns using T-Scan III before and after hydrostatic splint therapy on both healthy subjects and subjects with temporomandibular disorders. The main questions it aims to answer are: - Do occlusal forces for individual teeth differ before and after hydrostatic splint therapy? - Does the percentage distribution of forces across different sectors differ before and after hydrostatic splint therapy? Participants will: - Perform occlusal analysis using the T-Scan III device; - Use a hydrostatic splint for 30 minutes; - Perform a second occlusal analysis after using the hydrostatic splint. Researchers will compare healthy subjects and subjects with temporomandibular disorders to see if hydrostatic splint therapy makes a difference in the distribution patterns of occlusal forces.

NCT ID: NCT05827172 Completed - Clinical trials for Heart Failure With Reduced Ejection Fraction

AF Ablation for HF With Reduced EF

Start date: June 1, 2020
Phase: N/A
Study type: Interventional

This is an open label, multi-center, randomized parallel control clinical trial, to examining thethe clinical outcomes of AF ablation on HFrEF patients with persistent atrial fibrillation.

NCT ID: NCT05826821 Completed - Clinical trials for Heart Failure With Preserved Ejection Fraction

Biomarkers in HF: Circulating Biomarkers of Fibrosis and Cardiovascular Disease

Start date: March 2, 2017
Phase:
Study type: Observational

Heart failure with preserved ejection fraction (HFpEF) represents one of the largest unmet needs in cardiovascular medicine. Heart muscle scarring (myocardial fibrosis) is a key HFpEF disease mechanism and represents an important therapeutic target. Myocardial fibrosis can be measured non-invasively using the cardiovascular magnetic resonance imaging (MRI) extracellular volume (ECV) technique. However, some patients cannot undergo MRI scanning, and it is expensive. Circulating biomarkers in the blood that are sensitive to changes in myocardial fibrosis would represent an attractive cheaper and accessible alternative. This study aims to assess baseline levels of, and longitudinal change in, circulating biomarkers relating to fibrosis and cardiovascular disease in gifted samples from PIROUETTE trial participants, and evaluate the relationship between the biomarkers, anti-fibrotic treatment response and other study measurements.

NCT ID: NCT05826028 Completed - Clinical trials for Secondary Progressive Multiple Sclerosis

Mayzent (Siponimod) Onboarding of Secondary Progressive Multiple Sclerosis (SPMS) Patients With MSGo

Start date: July 9, 2020
Phase:
Study type: Observational

This study was a retrospective, non-interventional, longitudinal, descriptive study. This study did not have a key underlying hypothesis, rather it was designed to explore the onboarding and adherence of SPMS patients in Australia to Mayzent (siponimod) treatment. Initiating siponimod involves pre-screen tests, including a CYP2C9 genotype test to determine siponimod maintenance dosing, and patients underwent a 6-day titration prior to maintenance. The MSGo platform was developed to support onboarding. It is an integrated digital platform that functions as a patient support service.

NCT ID: NCT05825326 Completed - Clinical trials for Myeloproliferative Neoplasm

Epidemiological and Clinical-pathological Factors of Philadelphia-negative Myeloproliferative Neoplasms in Ecuador

Start date: January 1, 2012
Phase:
Study type: Observational

The goal of this observational study is to evaluate the epidemiological and clinical-pathological features of Philadelphia-negative myeloproliferative neoplasms through data from medical records

NCT ID: NCT05824598 Completed - Clinical trials for Heart; Surgery, Heart, Functional Disturbance as Result

Multifunctional Approach in Cardiac Surgery

TITANIC
Start date: May 15, 2023
Phase: N/A
Study type: Interventional

Postoperative pain and swallowing disorders are complex, multifactorial phenomenon that frequently occur after cardiac surgery. Preoperative anxiety and the interaction between sex and other sociocultural factors may predict greater sensitivity to postoperative pain, whereas the epidemiology and course of swallowing disorders has not been systematically investigated, along with the interaction between dysphagia, post-operative pain and emotional stress. Cardiac rehabilitation is a multifunctional intervention which may address all these functional domains, improving patients' prognosis. The aim of the present study is to demonstrate the superiority of a multifunctional approach (OMT, systematic swallowing screening and specific treatment according to good clinical practice associated with psychological counseling) compared to local clinical practice in the management of pain and swallowing disorders.

NCT ID: NCT05823389 Completed - Clinical trials for Chronic Periodontitis, Generalized

Flapless Emdogain in the Treatment of Periodontal Residual Pockets

Start date: September 2, 2019
Phase: N/A
Study type: Interventional

48 adult patients participated in a single-centre randomized clinical trial with split- mouth design. They had presented at re-evaluation after initial non-surgical periodontal therapy (steps 1 and 2 of periodontal therapy) for generalized periodontitis with at least 2 teeth with residual probing pocket depths (PPD) ≥5 and ≤8 mm, with bleeding on probing (BOP). Two teeth with similar PPD were randomized to receive re-instrumentation either with (test) or without (control) adjunctive flapless administration of EMD. Differences in the changes of PPD and BOP from baseline to 6 and 12 months will be analysed, and the frequencies of pocket closure (PPD ≤4 mm and no BOP) will be compared

NCT ID: NCT05821985 Completed - Clinical trials for Temporomandibular Joint Disorders

Evaluation of the Effect of Dextrose Prolotherapy Versus Dry Needling Therapy

Start date: September 1, 2023
Phase: N/A
Study type: Interventional

The hypertonic dextrose injection; Prolotherapy is a proliferation injection therapy that aims to trigger a low-grade inflammatory response inside the (TMJ), with the resultant captivation of abundant fibroblasts that regenerate and strengthen the tendinous and ligamentous attachments and stabilize the disc and the fibro-osseous junctions. On the other hand, dry needling' refers to the insertion of needles without the use of injectate. Dry needling is beneficial for treating a variety of neuromusculoskeletal pain syndromes as it represents a treatment modality for the ligaments and tendons, muscles, subcutaneous fascia, peripheral nerves, and neurovascular bundles. Deep dry needling (DDN) is a technique that utilizes the Intracapsular insertion of dry needles to approach the discal insertion to the lateral pterygoid muscle and the masseteric muscle origin, along the zygomatic bone and arch, aiming to inactivate the muscular trigger points (TPs).

NCT ID: NCT05821842 Completed - Clinical trials for Nasal Congestion and Inflammations

Sonu Nasal Congestion Relief Study in Patients Suffering From Moderate to Severe Nasal Congestion

SCORE
Start date: March 23, 2022
Phase: N/A
Study type: Interventional

To demonstrate the safety and effectiveness of Sonu for the treatment of patients suffering from moderate to severe nasal congestion.