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NCT ID: NCT04045379 Enrolling by invitation - Clinical trials for Postmenopausal Symptoms

LASER and Radiofrequency and Genitourinary Syndrome of Menopause

EPMLARF-arm1
Start date: August 5, 2019
Phase: N/A
Study type: Interventional

This is a randomized controlled trial to evaluate the use of LASER, Micro Ablative radiofrequency and topic strogen to treat symptoms of vulvovaginal atrophy of post menopause.

NCT ID: NCT04200937 Enrolling by invitation - Clinical trials for Erectile Dysfunction

IT Matters: The Erectile Restoration Registry

It MATTERS
Start date: August 5, 2021
Phase:
Study type: Observational

The primary objective of the It MATTERS registry is to assess erectile function at 6 months, post implantation of an It MATTERS Study Penile Prosthesis, demonstrating an improvement in quality of life from baseline.

NCT ID: NCT05217745 Enrolling by invitation - Clinical trials for Non-Alcoholic Fatty Liver Disease

MLCT Oil for Fatty Liver - PASS Trial

PASS
Start date: August 5, 2021
Phase: N/A
Study type: Interventional

The main objective of this randomised pilot study is to explore the relative efficacy of dietary MLCT oil versus LCT oil (corn oil) in augmenting therapy of overweight and obese NAFLD patients with at least a 1-stage reversal between F1 and F4.

NCT ID: NCT05887310 Enrolling by invitation - Clinical trials for Depressive Disorder, Treatment-Resistant

In Vitro Modeling of Drug-resistant Psychiatric Disorders Using Induced Pluripotent Cells

Start date: August 5, 2022
Phase:
Study type: Observational

Major depressive disorder (MDD), is a major medical and economic burden for today's society. About 30% of MDD patients develop treatment-resistant depression - TRD with the related sequelae in terms of worse prognosis. If several risk factors can be assessed readily on presentation, it can guide treatment planning and ultimately improve clinical outcomes. Currently, unlike other areas of medicine, poly-risk tools to facilitate this stratification in practice among patients with MDD are lacking but demanded in the era of personalised/precision medicine - a challenge that the project takes up. Ketamine - a glutamate N-methyl-d-aspartate (NMDA) receptor antagonist, is the first exemplary agent with rapid (within hours) antidepressant effects, even in TRD patients.Its mechanisms of actions (MoA) are still unclear but greatly demanded. So far, insights about ketamine's MoA come from preclinical animal studies but it's known that animal models have limited ability/effectiveness in mimicking the clinical complexity and were not subjected to sequential application of different treatments - a key requisite in humans to be defined as TRD. This ambitious inter/multidisciplinary project, has 3 goals: 1. To develop a clinical risk stratification tool for predicting TRD development. 2. To unravel ketamine's fast-acting antidepressant mechanisms of action (MoA) on mature neurons obtained from human induced pluripotent stem cells (iPSCs) obtained from (ketamine-responsive & non-responsive) patients with TRD. 3. To give maximum visibility to the project and spreading its contents & findings to and in a way understood by all target groups variously implicated/interested in project research & innovation.

NCT ID: NCT05991999 Enrolling by invitation - Stretch Clinical Trials

The Effect of Stretching of Swimming-related Muscles on 800-meter Swimming Performance in Master Swimmers.

Start date: August 5, 2023
Phase: N/A
Study type: Interventional

The study aimed to investigate the effect of stretching the sternocleidomastoid, pectoralis major and iliopsoas muscles on 800 meters freestyle swimming performance in master swimmers.

NCT ID: NCT04135001 Enrolling by invitation - Anger Clinical Trials

Mental Flexibility

MFS
Start date: August 6, 2019
Phase: N/A
Study type: Interventional

The main purpose of this research is evaluate if HBMT reduces HAB in Soldiers, reduces intra-team conflict, improves trust, and improves unit cohesion. A secondary purpose of this research is to test Soldier acceptability and perception of the training. Volunteers will be randomized to a training or placebo version of a computer task designed to reduce HAB and interpersonal conflict. Soldiers will then complete surveys at multiple time intervals before, during, and following deployment. If successful, this research would demonstrate the ability of a computer based training to improve unit cohesion and Soldier attitudes during pre-deployment training and deployment itself.

NCT ID: NCT03146546 Enrolling by invitation - Sepsis Clinical Trials

STUDY00015328: Sepsis Endotypes

Start date: August 6, 2020
Phase:
Study type: Observational

Determine the utility of blood resistin concentrations, when combined with clinical data, for predicting sepsis phenotypes that are associated with poor clinical outcomes. We hypothesize that resistin is a biomarker which provides critical prognostic information when used in conjunction with standard clinical data, in patients with sepsis and septic shock.

NCT ID: NCT04432285 Enrolling by invitation - Cervical Dystonia Clinical Trials

Long-term Outcome of DBS Versus Botulinum Toxin Treatment in Cervical Dystonia

Start date: August 6, 2020
Phase:
Study type: Observational

Cervical dystonia (CD) is the most common isolated dystonia in adults. Cervical dystonia symptoms can in most patients be managed well by botulinum toxin (BTX) injections, and supporting treatment measures. However, one-fifth to one-third of patients do not obtain sufficient relief from long-term BTX therapy, resulting in reduced quality of life. Deep brain stimulation (DBS) is a treatment method in which electrodes are surgically implanted permanently in the brain to modulate brain networks and function. In cervical dystonia, DBS of the postero-ventral part of the internal globus pallidus (GPi-DBS) has been established as an effective treatment for severe cases. However, the outcome of GPi-DBS in cervical dystonia has been reported mostly in some smaller series with up to 3 years follow-up. Thus, there is a lack of documentation of outcome of GPi-DBS in CD beyond 3 years of treatment and in larger patient materials. In this study the investigators will perform a long-term follow-up study of patients who were operated with a DBS-device targeting the GPi bilaterally, and who have been treated with chronic GPi-DBS for a minimum of 3 years. The investigators will measure the severity of symptom burden and quality of life with validated rating scales. The investigators will compare this DBS-treated cohort with an age- and gender matched group of CD patients who are receiving the standard treatment with botulinum neurotoxin (BoNT) injections and have been treated for at least 3 years as well. The investigators hypothesize that the DBS-treated group will have a significantly lower burden of symptoms at long-term follow-up than the BoNT treated group.

NCT ID: NCT05589532 Enrolling by invitation - Prosthesis Survival Clinical Trials

Single Tooth Implant-supported Fixed Prosthetic Rehabilitation Using PEEK.

PEEKPilotST
Start date: August 6, 2020
Phase: N/A
Study type: Interventional

The goal of this study is to evaluate the outcome of a Poly-ether-ether-ketone - used in single teeth implant-supported rehabilitations after one year of follow-up. The main question it aims to answer is: - What is the survival outcome of single teeth implant-supported prosthesis using Poly-ether-ether-ketone? The participants already rehabilitated with a single tooth dental implant will receive a definitive prosthesis incorporating Poly-ether-ehter-ketone.

NCT ID: NCT04839471 Enrolling by invitation - Clinical trials for Esophageal Squamous Cell Carcinoma (ESCC)

BI-754091 and Afatinib for Refractory Esophageal Squamous Cell Carcinoma (BEAR Study)

BEAR
Start date: August 6, 2021
Phase: Phase 2
Study type: Interventional

This is an open-label, single arm, multi-center study, assessing efficacy and safety of BI-754091 in combination with afatinib as treatment in patients with advanced or metastatic ESCC refractory to at least 1 line of systemic treatment (including chemotherapy or radiation therapy).