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NCT ID: NCT04707976 Recruiting - Multiple Sclerosis Clinical Trials

Comparing Transanal Irrigation With Navina Smart vs. Standard Bowel Care in Patients With Multiple Sclerosis

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

A randomized, superiority, controlled, interventional, prospective, multicentre, post-market study of TAI with Navina™ Smart versus Standard Bowel Care performed in a population of 92 subjects suffering from Multiple Sclerosis and confirmed Neurogenic Bowel Dysfunction. The study is expected to last for a total of 8 weeks per subject with two scheduled site visits.

NCT ID: NCT04707053 Recruiting - Surgery Clinical Trials

Data Collection and Analysis in Brainstem Surgeries

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

The hypothesis is that the structural documentation and analysis of the data of demographics, neuroimaging, IONM and clinical outcomes can help to further standardize the use of such equipment for detecting the integrity of the corticospinal tracts. We want to confirm that the retrospectively data analysis of neuroimaging, IONM and clinical outcomes does help to understand these methods better in the surgical management of brainstem lesions, and therefore, improve the safety of brainstem surgery.

NCT ID: NCT04705623 Recruiting - Postmenopausal Clinical Trials

Influence of Iyengar Yoga on the Bio-functional Age of Postmenopausal Women

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

The purpose of this Study is to find out if Iyengar-Yoga has a rejuvenating effect on women after menopause. The biofunctional status of the study participants will be assessed before and after a 12-week yoga program.

NCT ID: NCT04704414 Recruiting - Clinical trials for Graves Ophthalmopathy

Exophthalmometry With 3D Face Scanners

EX3D
Start date: August 14, 2019
Phase: N/A
Study type: Interventional

This study investigates diagnostic methods to measure eyeball protrusion with a smartphone face scanner compared to the traditional Hertel exophthalmometer. The study aims to validate a new reliable, fast and convenient smartphone app to measure the protrusion of the eyeball in different diseases such as Graves' disease, orbital tumors, orbital fractures or orbital inflammation, as well as other rare diseases.

NCT ID: NCT04703647 Recruiting - Clinical trials for Complex Regional Pain Syndrome Type I

Longitudinal Follow-up Study About Complex Regional Pain Syndrome (CRPS) Patients

Start date: March 14, 2019
Phase:
Study type: Observational

Complex regional pain syndrome (CRPS) is a post-traumatic chronic pain condition characterized by pain and other symptoms typically affecting a distal limb. Relatively little is known about the prognosis of the course of CRPS .Currently there is no specific test to diagnose CRPS. The primary objective of the study is to investigate prospectively the evolution of CRPS and the impact of the psychosocial factors on health status, recovery, quality of life, and working status of CRPS patients. The secondary objective of the study is to measure blood parameters in CRPS patients to investigate their evolution during the course of CRPS, and maybe to identify distinctive biomarkers associate with CRPS and that could be potential candidate for diagnosis.

NCT ID: NCT04702321 Recruiting - Childhood Cancer Clinical Trials

Genetic Risks for Childhood Cancer Complications in Switzerland

GECCOS
Start date: December 1, 2020
Phase:
Study type: Observational

The objectives of the GECCOS project are to identify genetic variants associated with complications of childhood cancer using genotype-phenotype association studies. Germline genetic samples and data of the "Germline DNA Biobank for Childhood Cancer and Blood Disorders Switzerland" (BISKIDS) which is included in the Geneva Biobank for Hematology and Oncology in Pediatrics (BaHOP) will be used with clinical data of Swiss childhood cancer patients collected at the Institute of Social and Preventive Medicine in Bern.

NCT ID: NCT04701567 Recruiting - Liver Diseases Clinical Trials

Diagnostic and Evaluation of Hepato-pancreatico-biliary Disease With MRI

Start date: June 30, 2020
Phase:
Study type: Observational

This is a retrospective review of images from patient data. There is no recruitment necessary for this study. Research Question: Can advanced multiparametric MRI techniques improve the detection and characterization of focal and diffuse liver disease, accurately assess treatment response and predict patient outcomes based on longitudinal monitoring? Hypotheses: Advanced multiparametric MRI techniques improve the detection, characterization and response assessment of focal and diffuse liver disease and can predict serious liver related outcomes.

NCT ID: NCT04701268 Recruiting - Rotator Cuff Tears Clinical Trials

Hemiverse Shoulder Prosthesis

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

This clinical trial investigates the safety and the preliminary clinical benefit of the hemiverse shoulder prosthesis. Implantation of this newly developed hemi-prosthesis is intended for patients who do not qualify for a regular reverse or hemi-prosthesis due to severe medical conditions, poor bone stock or critical status of the rotator cuff. The expected benefit is, that patients will have a minimally invasive surgical procedure, only addressing the humeral shaft, however with the biomechanical advantage of a total reverse shoulder prosthesis, meaning, that with a minimally invasive surgery a comparable result as with a regular total shoulder prosthesis is accomplished. Patients will be closely monitored within the study protocol for 24 months and thereafter in regular interval as with a normal prosthetic follow-up.

NCT ID: NCT04694885 Recruiting - Clinical trials for Breast Cancer Female

Quality of Life Improvement During Chemotherapy

QoLMa
Start date: July 31, 2021
Phase: N/A
Study type: Interventional

This study is a randomized controlled trial, taking place at the University Hospital Basel (CH). It aims at the alleviation of breast cancer patients' life quality during chemotherapy. The intervention group will participate in 10 sessions of structured hypnotherapy during the course of chemotherapy in addition to the standard of care. The control group will have access to the standard of care without any additional treatment. The main goal of the study is to investigate whether quality of life is higher among patients in the intervention group. Additionally, it will be analyzed if the interventions have a positive effect on chemotherapy side effects, symptoms of anxiety and depression and the immune system. Finally, the relative dose intensity (RDI) as well as treatment schedule adherence will be assessed. There are no risks to be expected from the intervention itself. In the case of positive findings, the standard of psycho-oncological care can be updated by integrating structured hypnotherapeutic interventions into the treatment of patients with breast cancer.

NCT ID: NCT04690660 Recruiting - Clinical trials for Postpartum Hypertension (PPHT)

Basel Postpartum Hypertension Cohort

Basel-PPHT
Start date: June 4, 2020
Phase:
Study type: Observational

This open label, prospective observational, single-center registry is to study short-, intermediate-and long-term course of postpartum hypertension and predictors/risk factors associated with long term cardiovascular and renal risk. Current disease management strategies will be evaluated.