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Syndrome clinical trials

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NCT ID: NCT04216147 Completed - Clinical trials for Carpal Tunnel Syndrome

Percutaneous Needle Electrolysis Versus Surgery in the Treatment of Carpal Tunnel Syndrome

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

The aim of this study is to compare the effectiveness of Percutaneous Needle Electrolysis (PNE) versus surgical treatment in the treatment of Carpal Tunnel Syndrome (CTS).

NCT ID: NCT04215380 Enrolling by invitation - Clinical trials for Polycystic Ovary Syndrome

Effects of Gum Arabic Ingestion on Hormonal and Metabolic Changes in Patients With Polycystic Ovary Syndrome

GA&PCO
Start date: January 25, 2020
Phase: N/A
Study type: Interventional

To assess the effects on hormonal and metabolic changes in the PCOs patients after ingestion of Arabic gum

NCT ID: NCT04214834 Active, not recruiting - Clinical trials for Neonatal Opioid Withdrawal Syndrome

Trial to Shorten Pharmacologic Treatment of Newborns With Neonatal Opioid Withdrawal Syndrome (NOWS)

Start date: September 8, 2020
Phase: Phase 3
Study type: Interventional

The objective of this study is to evaluate the efficacy of a rapid wean intervention compared with a slow-wean intervention in reducing the number of days of opioid treatment from the first dose of weaning to cessation of opioid among infants receiving an opioid (defined as morphine or methadone) as the primary treatment for neonatal opioid withdrawal syndrome (NOWS).

NCT ID: NCT04214470 Recruiting - Clinical trials for Irritable Bowel Syndrome

A Non-Interventional Pilot Study to Explore the Role of Gut Flora in IBS

Start date: March 2, 2020
Phase:
Study type: Observational

This study seeks to correlate microbiome sequencing data with information provided by patients and their medical records.

NCT ID: NCT04213677 Completed - Clinical trials for Polycystic Ovary Syndrome

Dapagliflozin Efficacy and Action in PCOS

DEAP
Start date: March 20, 2020
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the efficacy and safety of dapagliflozin on improving insulin resistance and hyperandrogenemia in obesity women with polycystic ovary syndrome.

NCT ID: NCT04213274 Not yet recruiting - Schnitzler Syndrome Clinical Trials

Study of the Efficacy and Safety of RPH-104 in Adult Subjects With Schnitzler Syndrome

Start date: May 2023
Phase: Phase 2
Study type: Interventional

The primary goal of the study is to assess the efficacy and safety of RPH-104 in subjects with Schnitzler Syndrome using Schnitzler Disease Activity Score (SDAS), which includes the Physician's Global Assessment (PGA) and the local laboratory C-reactive protein (CRP) result

NCT ID: NCT04213079 Completed - Clinical trials for Mal de Debarquement Syndrome (MdDS)

Treatments of Mal de Debarquement Syndrome (MdDS) by Habituation of Velocity Storage

Start date: June 15, 2020
Phase: N/A
Study type: Interventional

Mal de Debarquement Syndrome (MdDS) is an under-recognized but nevertheless common balance disorder, which in most cases occurs after exposure to prolonged passive motion. The current treatment approaches focus on reducing symptoms, but they can be retriggered. This project aims to shift the focus of MdDS treatment to permanently eliminating the symptom trigger while also minimizing symptoms.

NCT ID: NCT04212572 Recruiting - Clinical trials for Primary sjögren's Syndrome

Ultrasound Abnormalities of the Salivary Glands in Primary Sjögren's Syndrome According to the Duration of the Disease

MASAÏ
Start date: November 20, 2019
Phase:
Study type: Observational

Salivary gland ultrasonography is identified as a valuable diagnostic tool and potential criteria item for disease classification of sjögren's syndrome and evaluate evolution of parenchyma. The investigators have to include 242 patients. The objective is to evaluate the modification of ultrasonographic abnormalities according to disease in primary Sjögren syndrome.

NCT ID: NCT04212390 Recruiting - Clinical trials for MDS (Myelodysplastic Syndrome)

Personalized Medicine Program on Myelodysplastic Syndromes: Characterization of the Patient's Genome for Clinical Decision Making and Systematic Collection of Real World Data to Improve Quality of Health Care

FISiM-NGS-MDS
Start date: June 3, 2020
Phase:
Study type: Observational

BACKGROUND Myelodysplastic syndromes (MDS) typically occur in elderly people and with time, a portion of the patients evolve into acute myeloid leukemia (AML). Therefore a risk-adapted treatment strategy is mandatory. Current prognostic scores present limitations, and in most cases fail to capture reliable prognostic information at individual level. STATE OF THE ART Important steps forward have been made in defining the molecular architecture of MDS and gene mutations have been reported to influence survival and risk of disease progression in MDS. Evaluation of the mutation status may add significant information to currently used prognostic scores and a comprehensive analyses of large, prospective patient populations is warranted to correctly estimate the independent effect of each mutation on clinical outcome and response to treatments. AIMS In this project, the investigators will develop a research platform by integrating genomic mutations, clinical variables and patient outcome derived from real-world data obtained from FISiM (Fondazione Italiana Sindromi Mielodisplastiche) clinical network, including 72 hematological centers. This will allow the investigators to: 1. define the clinical utility of mutational screening in the diagnostic work-up and classification of MDS 2. assess the implementation of diagnostic and therapeutic guidelines (appropriateness) in the real-life 3. evaluate the impact of specific interventions (treatments) on clinical outcomes, long-term complications and costs 4. identify predictors of response to specific treatments, and develop precision medicine programs in hematology based on Real World Evidence RWD 5. measure patient-reported outcomes (PRO) and quality of life (QoL) in a real world MDS setting

NCT ID: NCT04209946 Active, not recruiting - Clinical trials for Respiratory Distress Syndrome

Early Caffeine and LISA Compared to Caffeine and CPAP in Preterm Infants

CaLI
Start date: January 22, 2020
Phase: N/A
Study type: Interventional

This study is being conducted to determine whether prophylactic administration of surfactant by the Less Invasive Surfactant Administration (LISA) method reduces the need for mechanical ventilation in the first 72 hours of life when compared to early Continuous Positive Airway Pressure (CPAP) alone.