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Calcinosis clinical trials

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NCT ID: NCT05662111 Recruiting - Fahr Syndrome Clinical Trials

Treatment of Ectopic Calcification in Fahr's Disease or Syndrome

CALCIFADE
Start date: April 3, 2023
Phase: Phase 2
Study type: Interventional

Fahr's disease or syndrome are neurodegenerative diseases in which patients present with bilateral vessel associated calcifications in the basal ganglia. The clinical penetration of Fahr's disease or syndrome is incomplete and heterogeneous comprising of neuropsychiatric signs, cognitive decline, movement disorders, and various other signs (migraine, speech disorders, pain, seizures). The symptoms start between 30 and 50 years and are (slowly) progressive. Symptomatic patients have an increased risk for dependence in activities of daily living and impaired quality of life. Currently, disease-modifying therapies are not available for patients with Fahr's disease or syndrome. However, in a small case series it was shown that alendronate was effective in the clinical treatment of several patients with Fahr's disease or syndrome. Now the time has come to investigate the effectiveness of treatment with bisphosphonates in patients with Fahr's disease or syndrome in a randomized controlled trial.

NCT ID: NCT05588895 Recruiting - Clinical trials for Coronary Artery Calcification

Picture of Incidental Calcium To Understand Risk Estimate (PICTURE) Trial

PICTURE
Start date: January 8, 2024
Phase: N/A
Study type: Interventional

This is a prospective randomized controlled trial assessing the impact of notifying patients and their clinicians of an incidental finding of coronary artery calcification (CAC) indicating increased cardiovascular risk. Patients will be identified through completed radiology orders for non-gated, non-contrast chest CT in the appropriate clinical context and then will have an EHR screen for inclusion criteria. The presence of CAC will be confirmed by a board-certified physician. Eligible patients will be randomized to CAC notification or usual care using a 1:1 stratified block randomization method based on baseline statin use.

NCT ID: NCT05556785 Recruiting - Clinical trials for Heart Failure With Preserved Ejection Fraction

Association of Epicardial Adipose Tissue Volume Axnd Radiodensity With Coronary Artery Calcification in Patients With HFpEF

Start date: January 1, 2020
Phase:
Study type: Observational

Recruiting patients who were diagnosed with HFpEF. Using Non-contrast CT to measure the total Agatston coronary artery calcification score, epicardial adipose tissue volume and attenuation. Analysing the correlation between them.

NCT ID: NCT05478902 Recruiting - Shoulder Pain Clinical Trials

Effectiveness of Non-surgical Management in Rotator Cuff Calcific Tendinopathy (THE EFFECT TRIAL)

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

The aim of this study will be to compare the effectiveness of an exercise therapy program with extracorporeal shockwave therapy, ultrasound-guided percutaneous irrigation and a wait and see approach in people with rotator cuff calcific tendinopathy.

NCT ID: NCT05451368 Recruiting - Clinical trials for Coronary Artery Calcification

Neointimal Features in Patients With Restenosis of Calcified Lesions

Start date: March 17, 2022
Phase:
Study type: Observational

Previous studies have suggested that restenosis (RS) after stenting is mainly due to smooth muscle cell proliferation and migration, but recent evidence suggests that in-stent restenosis(ISR) is associated with a number of factors. Coronary artery calcification is an independent predictor of ischaemia-mediated revascularisation 1 year after percutaneous coronary intervention (PCI) following RS.The characteristics of new neointima in patients with in-stent restenosis of calcified lesions are important issues to explore

NCT ID: NCT05444062 Recruiting - COPD Clinical Trials

Quebec Lung Cancer Screening PLUS Trial

QLC+
Start date: April 23, 2023
Phase: N/A
Study type: Interventional

Does an educational intervention for untreated COPD and cardiovascular disease which is integrated in an existing lung cancer screening program improve guideline concordant medication adherence at 12 months

NCT ID: NCT05417022 Recruiting - Angiography Clinical Trials

Safety and Efficacy Evaluation of Orbital Atherectomy System in de Novo Calcified Lesions

REFORCE
Start date: June 15, 2022
Phase:
Study type: Observational [Patient Registry]

This is a French, prospective, single-arm, multi-center registry to confirm the safety and efficacy of the Diamondback 360 TM Orbital Atherectomy System in the preparation of de novo calcified coronary lesions before implantation of a coronary endoprothesis in adult subjects. The primary safety endpoint is 30-day MACE and the efficacy endpoint is procedural success.

NCT ID: NCT05404204 Recruiting - Clinical trials for Coronary Artery Disease

The Efficacy and Safety of a Novel Adjunctive Pacing Strategy During Rotational Atherectomy

ROTA-PACE
Start date: February 1, 2021
Phase:
Study type: Observational

Coronary artery narrowings interfere with blood flow to the heart which can cause chest pain and heart attacks. Cardiologists can treat these narrowings with balloons and stents. However, some narrowings can become very calcified and hard making treatment with balloons and stents difficult. Rotational atherectomy is a tool to treat calcific coronary disease. It uses an ablative drill to break down the hardened plaques inside the coronary arteries facilitating subsequent treatment with balloons and stents. However, during this procedure patients can experience a slow heart rate which may compromise procedural safety. Cardiologists may use a temporary pacemaker that is inserted by separately accessing the heart through a large vein usually from the leg. This maintains a safe heart rate throughout the procedure. However, inserting the temporary pacemaker is associated with additional complications. We have developed and propose an alternative strategy to provide a temporary safety pacemaker during rotational atherectomy without the need for inserting an additional pacemaker.

NCT ID: NCT05301218 Recruiting - Clinical trials for Coronary Artery Calcification

CAlcified Lesion Intervention Planning Steered by OCT.

CALIPSO
Start date: December 15, 2021
Phase: N/A
Study type: Interventional

Calcified lesions are very frequent among coronary artery disease stenotic lesions. The prevalence of calcifications ranges from 30 to 40% (by angiography evaluation) but is higher when analyzed by intra coronary imaging. Calcified lesions are very frequent among coronary artery disease stenotic lesions. The prevalence of calcifications ranges from 30 to 40% (by angiography evaluation) but is higher when analyzed by intra coronary imaging. The presence of calcifications increases the risk of adverse evolution after PCI , including stent restenosis, thrombosis and need for repeat revascularisation. Specific and appropriate tools can be used for calcified lesions management , including high pressure non compliant balloons, intravascular lithotripsy and rotablator. Intra vascular OCT has a high sensitivity and specificity for calcium detection among coronary artery lesions. Compared to IVUS, OCT allows a better quantification of calcium sheets (depth extension ) . Several intra coronary imaging based calcified lesions management algorithms have been proposed , but none have been validated in clinical practice.

NCT ID: NCT05275088 Recruiting - Clinical trials for Failed Prosthetic Atrioventricular Valve/ Annulus Repair

Prizvalve® Transcatheter Atrioventricular Valve Replacement Study

Start date: March 9, 2022
Phase: N/A
Study type: Interventional

To evaluate the safety and performance of the Prizvalve® system in patients with severe atrioventricular annular calcification or failed prosthetic atrioventricular valve/ annulus repair.