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NCT ID: NCT05850429 Completed - Healthy Clinical Trials

BioDulse: The Effect of an Irish Seaweed Protein Extract on Glucose Control in Healthy Adults

BioDulse
Start date: May 9, 2023
Phase: N/A
Study type: Interventional

Co-ingesting protein with carbohydrate is an effective way to improve postprandial glucose handling. The investigators have isolated and identified a bioactive protein extracted from seaweed. The investigators aim to explore how varying doses of seaweed protein influence postprandial glycaemia and insulinaemia in a healthy population.

NCT ID: NCT05840978 Completed - Stress Clinical Trials

Effect of Probiotics on Stress in Young Adults

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

The study investigates the effects of probiotics in a young healthy population experiencing stress during a stress challenge, i.e. The Trier Social Stress Test (TSST).

NCT ID: NCT05801549 Completed - Clinical trials for Arterio-venous Fistula

Arterio-Venous Fistula Audit. Successful Utilisation Rates of Arterio-Venous Fistulae for Haemodialysis at University Hospital Limerick

Start date: September 13, 2022
Phase:
Study type: Observational

We wish to examine Arterio-Venous Fistula (AVF) and Arterio-Venous Graft (AVG) utilisation rates for Haemodialysis at University Hospital Limerick. We want to determine out of the AVF's that are surgically created, how many go on to be used as anticipated for haemodialysis treatments successfully.

NCT ID: NCT05783427 Completed - Clinical trials for Aspiration; Gastric Contents, Anesthesia

An Evaluation of a Liberal Hydration Regimen Before Elective Caesarean Section Using Beside Gastric Ultrasound

Start date: March 13, 2023
Phase:
Study type: Observational

The aim of this study is to compare the residual gastric volumes in non-labouring parturients prior to elective Caesarean delivery when fully fasted as per European Society of Anaesthesia pre-operative fasting guidelines against the 'Sip Til Send' fasting guideline via a paired cohort study. The primary hypothesis is that 'Sip Til Send' would be non-inferior to standard fasting at minimising the residual gastric volume prior to surgery.

NCT ID: NCT05749731 Completed - COVID-19 Clinical Trials

Pan-European Study on Geriatric Rehabilitation After COVID-19 Disease

EU-COGER
Start date: October 1, 2020
Phase:
Study type: Observational

Older and more vulnerable persons are more likely to get very ill when infected with the coronavirus, and have the highest COVID-19 morbidity and mortality rate. The majority of patients that are admitted to the hospital are older (>70 years), and some of them have been admitted to Intensive Care Units (ICU). In the case of rehabilitation of older patients post-COVID-19, we do not know what the course of recovery for these patients will be, and what treatment/approaches will deliver the best outcomes. Persons that are recovering from a COVID-19 infection, and admitted on a geriatric ward for early rehabilitation, or geriatric rehabilitation ward or facility, can be included in the study. They will receive routine, usual care; participation in this study will not affect their rehabilitation care. Routine care data will be collected from their electronic patient files at admission to geriatric rehabilitation, and at discharge. This also includes some data about their premorbid status. In addition, study participants will be called six weeks and six months after discharge from rehabilitation and asked some questions about their recovery. There is no risk association with participation in this study. Data will be anonymously collected in an online database. The primary aim of this study is to get insight into the course of recovery in (geriatric) rehabilitation patients affected by COVID-19 in Europe. Mainly, we are interested in functioning in activities of daily living (ADL-functioning) such as toileting, bathing, dressing, etc., and in quality of life. The second aim of this study is to get insight into the treatment modalities employed and the organization of geriatric rehabilitation that post-COVID patients in Europe receive. Therefore, we collect data on the types of care provided and the professionals involved. Moreover, we collect some patient characteristics such as year of birth, gender, date of admission and date of discharge; and data about complications such as delirium, pain, post-traumatic stress syndrome, hospital readmissions, and mortality. Our hypothesis is that most patients will show recovery during geriatric rehabilitation and in the six months after. However, we expect that the amount and/or speed of recovery will vary between patients.

NCT ID: NCT05739422 Completed - Stroke Clinical Trials

Online Neuropilates Classes in Chronic Stroke Patients: A Pilot Randomised Feasibility Study

Start date: November 16, 2022
Phase: N/A
Study type: Interventional

This study is being undertaken as part of a PhD qualification at ATU Sligo by the principal researcher Eimear Cronin. It will investigate the feasibility, safety and efficacy of a 6 week, online, remotely supervised neuropilates programme in post stroke participants as compared to a 6 week, online, remotely supervised generalised exercise programme and a 6 week unsupervised home exercise programme

NCT ID: NCT05735288 Completed - Dialysis Clinical Trials

Haemodialysis Outcomes & Patient Empowerment Study 03

HOPE-03
Start date: February 14, 2023
Phase:
Study type: Observational

This is a prospective, single-arm observational study that aims to assess the validity and reproducibility of an algorithm for assessing fluid status in a cohort of dialysis patients. The study will externally validate an existing algorithm for dry weight prediction in real-time in a cohort of dialysis patients.

NCT ID: NCT05733273 Completed - Hamstring Injury Clinical Trials

The Effect of 6 Week Hamstring Exercise Programs on Hamstring Muscle Function Performance in Female Athletes

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

This study aims to compare the effect of two hamstring strengthening programs on hamstring muscle strength in female university athletes. 60 participants will be recruited for this study. They will be randomly assigned to one of two 6-week hamstring strengthening programs, namely the single leg bridge exercise and the Nordic hamstring exercise protocol, and one control group. Eccentric and isometric hamstring strength, gluteal strength and will sprint speed will be measured before and after the intervention.

NCT ID: NCT05714410 Completed - Clinical trials for Constipation - Functional

Evaluation of Changes in Bowel Movement Frequency Following the Consumption of PHGG Compared to Placebo

TYPHOON-02
Start date: January 25, 2023
Phase: N/A
Study type: Interventional

Evaluation of Changes in Bowel Movement Frequency Following the Consumption of Partially Hydrolyzed Guar Gum (PHGG) in Adults With Constipation as Compared to Placebo (Typhoon 2)

NCT ID: NCT05711303 Completed - Clinical trials for Trans-epidermal Water Loss

Study to Investigate the Effect of Superba Boost on the Skin

Start date: March 13, 2019
Phase: N/A
Study type: Interventional

Study to determine the effect of 12 weeks daily consumption of Superba Boost as compared to placebo on reduction in Trans-Epidermal Water-Loss (TEWL).