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NCT ID: NCT05845567 Completed - Clinical trials for Drug Drug Interaction

The Potential of Givinostat as DDI Victim in Co-administration P-gp Inhibitor (Part 2)

Start date: March 21, 2022
Phase: Phase 1
Study type: Interventional

Primary objective: To assess the potential effect of oral Clarithromycin on the single-dose pharmacokinetics of Givinostat. Secondary objective: To assess the safety and tolerability of concomitant administration of Givinostat plus Clarithromycin.

NCT ID: NCT05840627 Completed - Healthy Clinical Trials

Acute Satiety and Metabolic Response of Daily Consumption of a Fruit Juice

Start date: February 28, 2023
Phase: N/A
Study type: Interventional

The "cLabel+ Innovative natural, nutritious and consumer-oriented clean label food" is a research and technological development project centered on responding to the challenges facing the food industry. It is focused on the concept of "clean label", which emerges as one of the major current trends in the sector, given the growing number of consumers who are increasingly aware and eager for information, who are looking for alternative, more transparent and natural food products. Thus, one of the aims of the cLabel+ project is to research the macronutrients and phenolic compounds present in food matrices and achieve a clean label positioning for the final products developed. This single group assignment clinical trial aims to evaluate the effect of daily consumption of a fruit juice, developed as part of the collaborative project cLabel+, on gut microbiota composition and diversity in healthy adults. It is also intended to study the acute metabolic effect, namely in terms of appetite control, and lipid and glucose metabolism.

NCT ID: NCT05814978 Completed - Shoulder Pain Clinical Trials

Effects of Scapular Therapeutic Exercise on Essential Biomechanical and Neurophysiological Parameters in Shoulder Pain Conditions With Scapular Impairments

Start date: March 27, 2023
Phase: N/A
Study type: Interventional

Shoulder pain is a prevalent and recurrent condition. After a period of shoulder pain, some adaptations could be found, as in scapular muscles and kinematics and/or in nervous system. It seems important to assess several biomechanical and neurophysiological outcomes to better characterize shoulder pain conditions and to program an intervention plane. Therapeutic exercise is one of the treatments used for shoulder pain, however there are still doubts and controversial findings regarding exercise focusing the scapular musculature. Thus, the present study aims to assess the effects of an intervention protocol based on scapular therapeutic exercise.

NCT ID: NCT05810922 Completed - Diet Habit Clinical Trials

Arbutus Berry - Intervention Study to Evaluate the Modulation of Intestinal Microbiota and Metabolic Parameters

F4F
Start date: November 8, 2022
Phase: N/A
Study type: Interventional

The tree that produces the arbutus berry, the strawberry tree, scientific name Arbutus unedo L., belongs to the family of Ericaceae. It exists in almost all of Southern Europe in arid and siliceous lands, in woods and forests and is very common in Portugal. Known for its use in the production of liqueurs and brandy, the arbutus berry is a fruit that can be consumed in nature or incorporated in the preparation of other foods. Arbutus berry has been attributed some properties beneficial to health given its low caloric value and its high content of vitamin C and flavonoids, which is why it is considered a good source of antioxidants. Arbutus has a high carbohydrate content (70-80% dry weight) with a relevant fiber fraction (10-30%), constituting an interesting source of vegetable protein (1-9%) and lipids (2-3%). Given this interesting nutritional composition, the hypothesis is that a daily consumption of this fruit can have an impact in health outcomes such as microbiota modulation and an improvement of metabolic parameters.

NCT ID: NCT05779072 Completed - Myopia Clinical Trials

Dual Focus Soft Contact Lens Wear Cessation Study

Start date: March 1, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the effect of ceasing treatment with dual focus soft contact lenses.

NCT ID: NCT05758103 Completed - Clinical trials for Peri-implant Mucositis

Limosilactobacillus Reuteri as an Adjuvant in the Treatment of Peri-implant Mucositis

LRRCT
Start date: January 5, 2022
Phase: N/A
Study type: Interventional

Mechanical debridement is the traditional method for the treatment of peri-implant mucositis and its success depends on the patient's correct oral hygiene. It is believed that probiotics may help by their ability to modulate the oral biofilm, resulting in anti-inflammatory and anti-bacterial plaque action. The aim of this study is to evaluate the adjuvant effect of the probiotic Limosilactobacillus reuteri in the mechanical treatment of peri-implant mucositis. This study aims to include 32 subjects with implant-supported total rehabilitation and peri-implant mucositis, divided into test and control groups, equally subjected to professional mechanical debridement, with the administration of a daily GUM® PerioBalance® lozenge for 30 days added to the test group. Plaque Index, Bleeding Index and probing pocket depth are evaluated before the intervention (baseline) and at 6 and 10 weeks later.

NCT ID: NCT05756374 Completed - Clinical trials for Children With Typical Development

OUT to IN: an Outdoor Body-oriented Intervention Program

Start date: January 4, 2021
Phase: N/A
Study type: Interventional

The goal of this randomized trial is to examine the effects of a body-oriented intervention program on preschoolers' social-emotional competence. The main question it aims to answer are: does OUT to IN effectively promotes preschoolers' self-awareness, self-regulation, relationship skills and motor competence? Participants are children between 3 and 6 years from portuguese preschools. The inclusion criteria are (a) participants' age between 3 and 6 years, (b) do not have participated in a similar intervention program within the last 6 months, and (c) do not have a physical condition that can affect the participation in the program. Children will be randomly allocated to the experimental group (who will participate in a 10-week intervention program with biweekly sessions of psychomotricity implemented outdoors) and to the control group (who will maintain their usual routines).

NCT ID: NCT05729815 Completed - Clinical trials for Social-emotional Competence

Body-oriented Interventions on Preschoolers' Social-emotional Competence

Start date: January 2, 2022
Phase: N/A
Study type: Interventional

Experimental study with 4 groups (3 experimental and 1 control). Examine the effects of 3 body-oriented intervention programs on preschoolers' social-emotional competence. Intervention programs focused on relaxation, loose parts play and combined loose parts play and relaxation, for 12 weeks with 2 30-min sessions per week.

NCT ID: NCT05729113 Completed - Renal Dialysis Clinical Trials

Pain Perception by the Chronic Renal Patient at the Time of Vascular Access Cannulation.

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

Pain in patients under hemodialysis affects chronic renal patients' quality of life. Distraction has been effective in controlling pain induced by the insertion of needles. Once applied adequately, distraction promotes endorphins' release, with efficacy in acute pain. This study aims to evaluate pain perception while puncturing the hemodialysis device using an anti-stress ball as a distraction strategy.

NCT ID: NCT05727748 Completed - Aging Clinical Trials

Effects of an Exercise Program With Augmented Reality

Start date: May 3, 2021
Phase: N/A
Study type: Interventional

The objectives of the present research is to observe the effects of a multimodal program with augmented reality on cognition, functional fitness, quality of life, and physical activity in older people.