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Syndrome clinical trials

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NCT ID: NCT05535543 Recruiting - Clinical trials for Acute Respiratory Distress Syndrome

Change in the Phase III Slope of the Volumetric Capnography by Prone Positioning in Acute Respiratory Distress Syndrome

Start date: September 6, 2022
Phase:
Study type: Observational [Patient Registry]

This study evaluates the effects of prone positioning on homogenization of ventilation.

NCT ID: NCT05535361 Recruiting - Clinical trials for Short Bowel Syndrome

A Feasibility Study to Evaluate Safety & Benefit of Eclipse XL1 System in Adult Patients With SBS

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

The Feasibility Study to Evaluate Safety and Probable Benefit of the Eclipse XL1 System in Adult Patients with Short Bowel Syndrome shall enroll up to 5 Subjects at up to 2 study sites in the United States.

NCT ID: NCT05534997 Not yet recruiting - Clinical trials for Post-COVID-19 Syndrome

Rehabilitation Therapy for Post COVID 19 Chronic Fatigue Syndrome

Start date: October 1, 2022
Phase: N/A
Study type: Interventional

The aim of this study is to investigate the effect of intensive combined rehabilitation therapy in form of Graded Exercise Therapy (GET) , Cognitive Behavioral Therapy (CBT) to treat patients with post COVID19 chronic fatigue syndrome .

NCT ID: NCT05534854 Recruiting - Clinical trials for Renal Cell Carcinoma

Frequency, Clinical Phenotype and Genetic Analysis of Heritable Kidney Cancer Syndromes

Start date: October 1, 2022
Phase:
Study type: Observational

This study will investigate the frequency, clinical phenotype, management and molecular genetic defects of heritable kidney cancer syndromes. Families with kidney cancer with known or suspected genetic basis will be enrolled. Affected individuals or individuals suspected of having a germline kidney cancer will undergo periodic clinical assessment and genetic analyses for the purpose of: 1) definition and characterization of phenotype, 2) determination of the natural history of the disorder, and 3) genotype/phenotype correlation. Genetic linkage studies may be performed in situations in which the genetic basis of the disorder has not been elucidated. This research will have a significant impact on the overall management of heritable kidney cancer syndromes patients and family members who are at risk for heritable kidney cancer syndromes. The study will ultimately facilitate the development of novel screening, prevention and treatment strategies for these individuals with the syndrome. In addition this study could have impact on the management of patients with personal and/or family history of heritable kidney cancer syndromes.

NCT ID: NCT05534828 Not yet recruiting - Clinical trials for Post Intensive Care Syndrome

Risk Factors for the Occurrence of Post Intensive Care Syndrome (PICS)

PICS3
Start date: October 2022
Phase:
Study type: Observational

Monocentric, observational, descriptive RIPH3 study with prospective data collection.

NCT ID: NCT05532423 Active, not recruiting - Metabolic Syndrome Clinical Trials

Nitrate Supplementation and Cerebrovascular and Cognitive Function in Metabolic Syndrome

Start date: December 1, 2022
Phase: Early Phase 1
Study type: Interventional

The purpose of this study is to determine if beetroot juice consumption can improve cognitive performance and brain vascular function in individuals with metabolic syndrome

NCT ID: NCT05530005 Recruiting - Clinical trials for Subacromial Impingement Syndrome

Traditional Physiotherapy Protocol vs Prescribed Exercises in Impingement Syndrome of the Shoulder

Start date: June 1, 2022
Phase: N/A
Study type: Interventional

Pain and limitation of shoulder mobility resulting from sub-shoulder syndrome called sub acromion impingement syndrome (SIS) are a big social problem in highly developed countries. This work aims to compare the method of treating SIS ailments taking into account the monitored exercises on their own- hands off, to the traditional method of individual physiotherapy considering manual therapy, TENS and local cryotherapy- hands on. The study will qualify people aged 18-50 years without previous injections, surgical procedures and physiotherapy within the shoulder joint. The initial examination of the participants will include: ultrasound examination, Neer test, functional mobility test according to FMS, clinical examination: palpation of the joint area, cross body adduction test, radial artery pulse test, numerical pain scale 0-10, DASH questionnaire. After the initial checkups, 60 people will be qualified for the proper examination. Selected participants will be divided into two groups of 30 people, each group consisting of 15 women and 15 men. The first group will undergo self-therapy for 3-5 months. The subjects will exercise independently for about 1.5 hours a day, three times a week. Every two weeks, each subject will be admitted to a follow-up visit, during which the physiotherapist will recommend another set of exercises and check the progress. The second group will undergo traditional physiotherapy three times a week for a period of three months. After a period of 3-5 months, both groups will undergo the same examination as initially. The results of both studies will be compared in both groups. The groups will then be compared to each other.

NCT ID: NCT05529108 Active, not recruiting - Diabetes Clinical Trials

Glycaemic Control Effect of BSG and Underlying Gut - Related Mechanism in Singapore Adults With Metabolic Syndrome

Start date: October 28, 2022
Phase: N/A
Study type: Interventional

The purpose of this research project is to assess the glycaemic controlling effects of consuming BSG and bio-transformed BSG-containing biscuits and its underlying gut - related mechanism in adults with MetS using in-vivo setting.

NCT ID: NCT05529095 Not yet recruiting - Clinical trials for Restless Legs Syndrome

Sublingual Apomorphine in Refractory Restless Legs Syndrome

Start date: September 1, 2022
Phase: Phase 4
Study type: Interventional

This is an open label, short placebo-controlled trial in Restless Legs Syndrome (RLS) patients inadequately treated with standard therapy. Investigators hypothesize that the study drug, sublingual apomorphine (Kynmobi), may improve RLS breakthrough symptoms. This study is designed to determine if sublingual apomorphine improves breakthrough symptoms in RLS patients, in addition to subjective responses.

NCT ID: NCT05528900 Recruiting - Clinical trials for Food Protein Induced Enterocolitis Syndrome (FPIES)

A Multicentre French Prospective Study of Children With Food Protein Induced Enterocolitis Syndrome in Its Acute Form

SEIPA-FPIES
Start date: March 31, 2023
Phase: N/A
Study type: Interventional

Food protein induced enterocolitis syndrome (FPIES), is a non-IgE mediated food allergy (FA) which seems to expand, and occurring in infancy. This disease is usually unknown by clinicians. In 2017, an international workgroup of American Academy of Allergy, Asthma and Immunology published clinical criteria to specify the diagnosis. However, there is a lack of information in literature for describe the evolution and atypical phenotypes. In addition, no prospective French series has been published to date. The aim of the study is to collect clinical features and allergy testing of children who have acute form of FPIES at diagnosis and during evolution during three years