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Interventional clinical trials

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NCT ID: NCT06468046 Not yet recruiting - Interventional Clinical Trials

Mama Empoderada: Adapting a Novel Mental Health Prevention Intervention for Migrant Mothers With Young Children

Start date: July 2024
Phase: N/A
Study type: Interventional

This pilot randomized controlled trial (RCT) will test a theory-based intervention [Mamá Empoderada' (Mom Power)] to promote mental health and positive parenting among migrant mothers with young children.

NCT ID: NCT06054620 Recruiting - Interventional Clinical Trials

The Effect of Exercise and Presleep Nutrition on Muscle Connective Tissue Remodelling

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

The primary objective of this study will be to determine the influence of a presleep vitamin C-enriched, collagen-modelled supplement (CVC) on the metabolic fate of dietary glycine using a [2H5]glycine tracer within the intramuscular connective tissue at rest and after a bout of resistance exercise. Other outcomes will be related to regulation collagen remodelling in skeletal muscle.

NCT ID: NCT05754125 Active, not recruiting - Interventional Clinical Trials

In Vivo and in Vitro Anabolic Potential of Essential Amino Acids Following Resistance Exercise

DiEx
Start date: January 21, 2023
Phase: N/A
Study type: Interventional

This study seeks to investigate the anabolic potential of a dileucine-enriched essential amino acid (EAA) formulation compared with a branched chain amino acid (BCAA) alternative and a collagen beverage on muscle protein anabolism and catabolism following a bout of resistance exercise training. To do this, investigators will employ a novel 'breath test' method developed in our laboratory as well as blood and urine sampling. The results of this study will allow us to better understand the anabolic potential of dileucine which could have implications for people engaging in regular resistance training (such as athletes) as well as people that need to preserve muscle mass (older people who are susceptible to anabolic resistance and sarcopenia, or muscle wasting).

NCT ID: NCT05554653 Active, not recruiting - Interventional Clinical Trials

Influence of Leucine Enriched Amino Acids on Myofibrillar and Collagen Protein Synthesis

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

The primary objective will be to determine the effect of leucine-enriched essential amino acids (LEAA) compared to carbohydrate placebo on dietary incorporation of [D5] Phenylalanine & [D5] Glycine into the three skeletal muscle protein pools (myofibrillar, sarcoplasmic and collagen), both following resistance exercise and at rest, with the two tracers provided as a 'intrinsically labeled' bolus. Other outcomes will relate to molecular regulation of protein synthesis.

NCT ID: NCT05336708 Completed - Interventional Clinical Trials

The Effect of Acupressure on Fatigue

Start date: September 27, 2021
Phase: N/A
Study type: Interventional

In this study, it is aimed to determine the effect of acupressure on fatigue in nursing students.

NCT ID: NCT05145712 Recruiting - Interventional Clinical Trials

Quantitative Bowel Readiness Assessment System in Predicting the Missed Detection Rate of Adenomas

Start date: July 21, 2021
Phase: N/A
Study type: Interventional

To verify the correlation between the proposed artificial intelligence based bowel preparation assessment system and the missed detection rate of adenomas, and to evaluate whether the system can effectively assist doctors in identifying patients who need to be re-examined by colonoscopy due to poor intestinal cleanliness.

NCT ID: NCT05060484 Recruiting - Prevention Clinical Trials

A Phase II Study of SCT1000 in Healthy Women Aged 18 to 45 Years

Start date: October 19, 2021
Phase: Phase 2
Study type: Interventional

A phase II random, double blind, positive and placebo control trail was conducted in 1200 healthy women in the arm A: 18-26 years old and 600 healthy women in the Arm B: 27-45 years old. The 1800 subjects to be inoculated with middle, and high dose vaccine. Middle dose SCT1000: hight dose SCT1000: placebo: positive control =1:1:1:1.Two arms can be recruited at the same time. If the DSMB assessment shows that the adverse events of a certain dose group meet the criteria of suspension / termination, the dose group will be suspended / terminated.

NCT ID: NCT03921164 Recruiting - Radiography Clinical Trials

Non Invasive Use of Pressure-Volume Loop in the Operating Room

LOOPING
Start date: January 27, 2021
Phase:
Study type: Observational

In patients under general anesthesia, the prevention of intraoperative hypotension to maintain blood pressure (BP) close to the initial blood pressure, i.e. before anesthesia, is essential to reduce the risk of death and improve surgical outcomes. Vasoactive agents are commonly used to correct this hypotension (Phenylephrine Ephedrine Noradrenaline). These three vasoconstrictors have specific effects on the afterload of the heart and can impair its function. The analysis of the left ventricular pressure-volume curve (PV Loop) allows continuous information on the post-charge state of the left ventricle and the changes induced by the vasoconstrictors to be observed. However, the investigators currently have no way of monitoring these effects. In clinical practice if these loops are obtained non-invasively they can be used in the evaluation of cardiac function of at-risk patients in perioperative and also in intensive care to allow therapeutic adaptation.

NCT ID: NCT03876379 Completed - Orthopedic Surgery Clinical Trials

Brain Power Spectral Density Under Propofol

PROBRAIN
Start date: January 24, 2015
Phase:
Study type: Observational [Patient Registry]

In the operating room, the state of anesthesia is monitored during general anesthesia-induced hypnosis through EEG-based neuro-monitoring. Recent studies suggest that variables extracted from per-operative EEG change as brain ages. Furthermore, aging is itself an independant factor associated to an increased sensitivity to General Anesthesia (GA). Among fragility sign, per-operative Burst Suppression (BS) has been associated to a poor postoperative cognitive trajectory. The main goal of this observational clinical study is to extend the traditional use of per-operative EEG to the detection and prediction of various degrees of brain fragility, depending on the depth of anesthesia (DoA).

NCT ID: NCT03853226 Completed - Radiography Clinical Trials

Rational for the Use of Velocity-Pressure Loop in the Operating Room

VPLOOP
Start date: January 5, 2014
Phase:
Study type: Observational

In surgical patients considered with "high cardiovascular risk", by their field or by the nature of their intervention, it is recommended to use hemodynamic monitoring including a continuous measurement device of arterial pressure and cardiac output (CO). However, targeting mean arterial pressure (MAP) with boluses of selective peripheral vasopressors (without positive inotropic or chronotropic effects) could have deleterious effects on CO. Thus, it seems important to use a combined analysis of MAP and CO to estimate the afterload-related cardiac performance (ACP) The investigators recently proposed a cardiac afterload monitoring, in the descending thoracic aorta, based on a combined analysis of flow velocity signal recorded by trans-oesophageal Doppler and aortic pressure, the Velocity-Pressure Loop (VP Loop). VP Loop, and its derived indicators, especially Global AfterLoad Angle (GALA), could be useful during hemodynamic management for continuous cardiac afterload monitoring. However, in cardiology unit, cardiac afterload is usually measured at the ascending aorta behind the aortic valves. The main objective of this study is to compare VP Loop parameters build in the ascending and descending thoracic aorta according to patient cardiovascular risk factors.