Clinical Trials Logo

Filter by:
NCT ID: NCT04521504 Completed - Rotator Cuff Tears Clinical Trials

The ISEO Biofeedback Tool During the Rehabilitation of Patients Treated for Rotator Cuff Tear

PDT1-1
Start date: November 21, 2017
Phase: N/A
Study type: Interventional

The present study addresses the issue about post-surgical recovery process, for patients arthroscopically treated for rotator-cuff tear. The aim of the research is to test the effectiveness of a new rehabilitation protocol that includes kinematic biofeedback with the motion analysis system ISEO.

NCT ID: NCT04521361 Active, not recruiting - Clinical trials for Bone Metastatic Castration-resistant Prostate Cancer

A Study to Assess How Radium-223 Distributes in the Body of Patients With Prostate Cancer Which Spread to the Bones

Start date: November 16, 2020
Phase: Phase 1
Study type: Interventional

In this study researcher want to gain more information on how the study drug (radium-223) is distributed in the bone, particularly in the tumor free bone in participants with prostate cancer. The study plans to enroll 60 patients with the age of at least 18 years and suffering from prostate cancer which has spread to the bones. Researcher will divide the study participants into 2 groups. Patients in Group 1 should have up to 6 bone metastases and patients for group 2 should have more than 6 bone metastases. The study medication will be given as injection into a vein every 4 weeks up to a maximum of 6 times. To study how radium distributes in the body and particularly in the bones, participants will undergo after study medication intake MRI or CT Scans (imaging techniques).

NCT ID: NCT04521231 Recruiting - Clinical trials for B Cell Precursor Acute Lymphoblastic Leukemia

A Study of Subcutaneous Blinatumomab Administration in Acute Lymphoblastic Leukemia (ALL) Patients

Start date: January 4, 2021
Phase: Phase 1/Phase 2
Study type: Interventional

The study aims to evaluate the safety, efficacy, and tolerability of subcutaneous (SC) blinatumomab for treatment of Acute Lymphoblastic Leukemia (ALL), to determine the maximum tolerated dose (MTD), and recommended phase 2 dose(s) (RP2D) of SC administered blinatumomab. It will also conduct a clinical PK evaluation of SC1 and SC2 blinatumomab formulations.

NCT ID: NCT04520997 Completed - Clinical trials for Lower Face Folds and Lines

Restylane Defyne in a Stepwise Treatment Approach

Start date: December 7, 2020
Phase: N/A
Study type: Interventional

This was a 12-week study to evaluate the effectiveness and safety of Restylane Defyne when using two different injection approaches, stepwise down-up vs. top-down, when treating the lower face.

NCT ID: NCT04520451 Active, not recruiting - Clinical trials for Immunoglobulin G4 Related Disease

Open Label Two-Arm Study to Evaluate Rilzabrutinib in IgG4-Related Disease Patients

Start date: August 22, 2020
Phase: Phase 2
Study type: Interventional

This is a Phase 2a, multi-center, open-label, two-arm study of approximately 25 patients with active IgG4-related disease (IgG4-RD). The two arms include (1) Experimental: rilzabrutinib with glucocorticoids and (2) Active Comparator: glucocorticoids only.

NCT ID: NCT04520347 Enrolling by invitation - Clinical trials for Ventricular Tachycardia

IVTCC 2.0: A Prospective Multicenter Ventricular Tachycardia Catheter Ablation Registry

IVTCC
Start date: December 1, 2018
Phase:
Study type: Observational [Patient Registry]

This is a prospective multi-center international registry. The objective of this registry is to collect prospective data on patients undergoing catheter ablation for Ventricular Tachycardia (VT) and Premature Ventricular Contractions (PVC). The registry will be used for clinical monitoring, research, and quality improvement purposes.

NCT ID: NCT04520087 Recruiting - Clinical trials for Shoulder Instability

Clinical and Radiographic Assessment After Surgical Treatment of Anterior Shoulder Dislocation

Start date: October 13, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the clinical and radiographic results after surgical treatment with implant-free allograft in the treatment of Anterior Shoulder Dislocation and to assess the safety of the surgery.

NCT ID: NCT04519827 Completed - Allergy;Food Clinical Trials

A Hypoallergenicity Study on a New Rice-Based Hydrolysate Formula

CHARM
Start date: May 21, 2020
Phase: N/A
Study type: Interventional

Cow's Milk Allergy (CMA) affects between 2-3% of young children but its severity varies between regions/countries. While the long-term prognosis for CMA is good, with the majority (80-90%) of children outgrowing their allergy by around 3-5 years. Breast feeding is the most optimal form of feeding for all infants, regardless of their condition, and in those with CMA maternal dairy exclusion is recommended as first line treatment. In non-breast fed or mixed feeding, a hypoallergenic milk substitute is recommended for young infants. The AAP and other societies such as EAACI and ESPGHAN considers a formula to be 'hypoallergenic' if at least 90% of children with documented CMA tolerate it, with a 95% CI, under double-blind, placebo-controlled conditions.This equates to at least 29 children who should tolerate the product following blind and open challenge.

NCT ID: NCT04516941 Terminated - COVID-19 Clinical Trials

CorONa Virus edoxabaN ColchicinE (CONVINCE) COVID-19

CONVINCE
Start date: January 21, 2021
Phase: Phase 3
Study type: Interventional

There is emerging evidence that patients with SARS-CoV-2 are affected by increased coagulopathy, including in the most advanced forms, a fully blown disseminated intravascular coagulation, leading to multi organ failure (MOF). Post-Morten observations from patients who died because of SARS-CoV-2 infection in Bergamo, Italy and other places have revealed the presence of diffuse venous, arterial and microcirculatorythrombosis, not only restricted to the lung but also involving the kidneys, heart and gut. Thrombin plays a central role in mediating clot forming as well as in mediating inflammation. A direct factor X inhibitor, namely edoxaban can act as prophylactic measure to mitigate the risk of venous and arterial thrombotic complications. Colchicine is an inexpensive (generic drug), orally administered, and a potent anti-inflammatory medication. It might accelerate SARS-CoV-2 clearance. The aim of the CONVINCE study is therefore to assess the safety and efficacy of edoxaban and/or colchicine administration in SARS-CoV-2 infected patients who are managed outside the hospital with respect to the occurrence of fatalities, hospitalisation, major vascular thrombotic events or the SARS-CoV-2 clearance rate under RT PCR.

NCT ID: NCT04515680 Completed - Iron Overload Clinical Trials

Endocrine Function During Deferasirox Therapy

Start date: November 2, 2016
Phase:
Study type: Observational

A national survey on the prevalence and natural history of endocrine complications in thalassemia transfusion--dependent patients treated with deferasirox was designed, in order to assess a larger population during a longer follow up and improve the quality of previous investigations.