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NCT ID: NCT04952662 Completed - Injuries Clinical Trials

Candidate Gene Association Study With Injury in Elite Male Youth Football Players

Start date: December 1, 2019
Phase:
Study type: Observational

Understanding how candidate genes, previously associated with injury susceptibility, influence the incidence of muscle, bone, ligament, and tendon injuries across the development pathway of elite footballers may provide valuable insight into inherent injury predisposition to support the long-term development of every individual. Therefore, the aim of the present study was to investigate the association between candidate genetic variants and muscle, bone, ligament, and tendon injuries in elite football with sub-analysis of the influence of age and maturation on injury susceptibility.

NCT ID: NCT04952467 Completed - Healthy Volunteers Clinical Trials

Single-dose Mass Balance Recovery and Metabolite Profile and Identification of 14C-XEN1101

Start date: July 14, 2021
Phase: Phase 1
Study type: Interventional

This study will evaluate the mass balance recovery and metabolite profile, and will identify metabolite structures following a single oral dose of 14C-XEN1101 in healthy adult male subjects.

NCT ID: NCT04951687 Completed - Cognitive Change Clinical Trials

Acute and Chronic Effects of Ecologic Barrier© on Mood and Cognition

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

This study aims to investigate the acute and chronic effects of an 8 week probiotic intervention (Ecologic Barrier©) on mood and cognitive outcomes in healthy adults.

NCT ID: NCT04951076 Completed - Clinical trials for Post-Traumatic Stress Disorder

A Phase 2b Study of BNC210 Tablet Formulation in Adults With Post-Traumatic Stress Disorder (PTSD)

ATTUNE
Start date: July 27, 2021
Phase: Phase 2
Study type: Interventional

The purpose of this study is to assess the effects of BNC210 compared to placebo on PTSD symptom severity as measured by CAPS-5 Total Symptom Severity Scores.

NCT ID: NCT04950257 Completed - Rumination Clinical Trials

Evaluating the Effects of a Self-help Mobile Phone Application on Worry and Overthinking in Young Adults Aged Between 16 and 24.

Start date: May 14, 2021
Phase: N/A
Study type: Interventional

This project seeks to understand if a new self-help mobile phone application (called MyMoodCoach) is effective at reducing worry and overthinking, prominent risk factors that predict reduced well-being and poor mental health. As a primary outcome, the investigators are predicting that people who use the app will report more significant reductions on measures of overthinking than those who do not. The investigators also predict that people who use the app will report more significant reductions in measures of worry as well as reported symptoms of depression and anxiety. Further, it is predicted that people who use the app will report a significantly higher increase in their well-being compared to those who do not.

NCT ID: NCT04949841 Completed - Chronic Hand Eczema Clinical Trials

Open-label Multi-site Extension Trial in Subjects Who Completed the DELTA 1 or DELTA 2 Trials

DELTA3
Start date: August 23, 2021
Phase: Phase 3
Study type: Interventional

The purpose of this extension trial is to evaluate the long-term safety of delgocitinib. Subjects will visit the clinic every 4 week to assess the safety and efficacy of the treatment, until Week 36. A final follow-up phone call is planned on Week 38.

NCT ID: NCT04948255 Completed - Covid19 Clinical Trials

Measuring Work-Related Stress in Primary Care in the Covid-19 Pandemic

WRS
Start date: April 1, 2019
Phase:
Study type: Observational

This prospective cohort study was designed to assess WRS amongst clinical and non-clinical staff in a primary healthcare setting using a validated tool with a view to developing an evidence base to form a historical and comparative record during the Covid-19 pandemic.

NCT ID: NCT04948086 Completed - Blood Pressure Clinical Trials

Blood Pressure and Central Haemodynamics in Healthy Adults Stratified by MTHFR Genotype

RAFA Obs
Start date: June 28, 2011
Phase:
Study type: Observational

Approximately 12% of the world's population have a have a common C677T polymorphism in the gene encoding the folate metabolising enzyme, methylenetetrahydrofolate reductase (MTHFR). Homozygosity for the polymorphism (TT genotype) appears to result in an increased requirement for the B-vitamins folic acid and riboflavin and more importantly results in an increased risk of developing high blood pressure (BP). Previous work from our Centre has demonstrated significantly higher BP in those with the TT genotype. This work has been conducted in cohorts with premature cardiovascular disease (CVD) and hypertension without overt CVD, but the effect in younger, healthier individuals is unexplored. To date our studies have also focused on BP as the primary outcome, but newer markers of vascular health including central pressure and hemodynamics have emerged as superior prognostic indicators of CVD. The effect of the TT genotype on these measures is thus an important area for investigation and may help us understand the mechanism linking the genotype with BP, which is currently unknown. As adults with the TT genotype appear to have increased requirements for riboflavin and folic acid, and BP in TT adults appears to be riboflavin dependent, the influence of these vitamins on central measures is an area for consideration. Study Design This is an observational study investigating the blood pressure profiles of healthy adults aged 18-65 years, stratified by MTHFR genotype. Apparently healthy adults will be recruited from workplaces and the general community across Northern Ireland and screened for the polymorphism via buccal swab. Those with the TT genotype and a similar number of non-TT (i.e. CC/CT) genotype individuals will be contacted and asked to come to attend a one-off appointment. Brachial BP will be assessed by an electronic BP monitor, central BP and central haemodynamics (augmentation index, augmentation pressure and pulse wave velocity) will be assessed by SphygmoCor XCEL. In addition, anthropometric measurements, health and lifestyle information and a blood sample will be obtained. Data will be statistically analysed using SPSS software to if determine differences between gentoype groups exist.

NCT ID: NCT04945083 Completed - Clinical trials for Gastrointestinal Tolerance

Evaluation of a High Protein, High Calorie Pudding in Adults With/or at Risk for Malnutrition

Start date: January 13, 2021
Phase: N/A
Study type: Interventional

This is a multi-center, prospective, non-randomized, non-blinded, single-arm, single treatment study to evaluate the tolerance of a nutritional pudding.

NCT ID: NCT04943471 Completed - Myodesopia Clinical Trials

Personality Traits in Patients Seeking a Consultation for Treatment for Floaters

Start date: December 15, 2021
Phase:
Study type: Observational

This study aims to assess if certain personality traits are move prevalent in patients seeking consultation for treatment of floaters, despite good visual acuity and no other ocular pathology compared to the normal population.