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Healthy Individuals clinical trials

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NCT ID: NCT05358561 Recruiting - Healthy Individuals Clinical Trials

Postprandial Glucose, Insulin and Subjective Saturation Response in Healthy Individuals

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

This study is a pioneering study in which the effect of the consumption of cakes produced with the addition of cereal-like products such as chia and flax seeds, which have high soluble fiber content, on blood glucose and insulin values, and the effect on the satiety response of individuals after consumption of cakes, will be a pioneer in many subjects. As a result of the study, the relationships between the changes in the investigated parameters and the possible changes in these parameters will be revealed. The results obtained suggest that foods rich in soluble fiber such as chia and flaxseed and foods produced with the possible synergetic effect of chia and flaxseed are used in healthy and safe products suitable for our consumption habits, and that these products are both protective and protective against the development of complications such as obesity and type 2 diabetes, cardiovascular diseases. The investigators think that it may also play a role in preventing its progress.

NCT ID: NCT05110885 Not yet recruiting - Clinical trials for Duchenne Muscular Dystrophy

Public AttitudesTowards SMA and DMD Awareness, Newborn and Carrier Screening and Physiotherapy Practices

Start date: November 2021
Phase:
Study type: Observational

The addition of SMA and DMD muscle diseases to newborn screening and premarital carrier screening has been controversial. In this study, researchers aim to measure the awareness level of SMA and DMD muscle diseases of individuals living in Turkey and to obtain information about their attitudes towards newborn and carrier screening and physiotherapy practices. Thus, this study aimed to determine the factors that affect people's views on this subject.

NCT ID: NCT05011968 Completed - Healthy Individuals Clinical Trials

Intervention Study on Iodine Biofortification Vegetables ( Nutri-I-Food

Nutri-I-Food
Start date: March 1, 2019
Phase: N/A
Study type: Interventional

The aim of the project is to study of the influence of Lettuce crop enriched with Iodine on Thyroid hormone synthesis. Secondary outcome to find out iodine presence in urine in order to evaluate vegetables, like little crop, as Iodine biocarrier

NCT ID: NCT04941196 Completed - Healthy Individuals Clinical Trials

Bioequivalence Study of Anplag® 90mg (Ticagrelor) Tablet & Brilinta® 90 mg (Ticagrelor) Tablet in Healthy Adult Male Pakistani Subjects Under Fasting Condition

BE
Start date: October 16, 2020
Phase: Phase 1
Study type: Interventional

Single oral administration of study drugs (i.e. Anplag® & Brilinta®) in Two periods after at least 10 hours fasting. The periods will be separated by a washout period of 7 days. The purpose of this study is to compare the bioavailability of Anplag® 90mg (Ticagrelor) Tablet with Brilinta® 90 mg (Ticagrelor) Tablet under fasting conditions in healthy Pakistani male subjects.

NCT ID: NCT04873570 Completed - Healthy Individuals Clinical Trials

Bioequivalence Study of Mofest® 400mg (Moxifloxacin) Tablet With Avelox® 400mg (Moxifloxacin) Tablet in Healthy Pakistani Subjects

BE
Start date: May 28, 2021
Phase: Phase 1
Study type: Interventional

Single oral dose, of test and reference Tablet will be administered to healthy volunteers, after at least 10 hours fast together with 240 mL of ambient temperature water at their scheduled dosing time-points. Blood samples will be taken up to 72.0 hours post-dose.

NCT ID: NCT04830098 Completed - Healthy Individuals Clinical Trials

Comparison of the Effectiveness of Spinal Stabilization Exercises and Chiropractic Spinal Manipulation

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

It is the study of the effectiveness of spinal stabilization exercises and chiropractic spinal manipulation in healthy individuals. In addition, it was planned to investigate the effects of spinal stabilization exercises and manipulation on muscle strength, muscular endurance, balance and proprioception, depression and quality of life.

NCT ID: NCT04772417 Completed - Healthy Individuals Clinical Trials

The Effects of Standardized vs Individualized Seat Height on 1-minute Sit-to-stand Performance

ESTI-STS
Start date: April 20, 2021
Phase:
Study type: Observational

The 1-minute sit-to-stand test (1MSTS) is a widely used functional capacity test and has promising predictive potential. Current standards of practice suggest the use of a chair with a standardized height. However, this practice makes the test more demanding for taller individuals than for shorter individuals. This implies over- or underestimation of functional capacity depending on body morphology. Therefore, the aim of this study is to investigate the influence of knee joint angle, femur length and bodyweight on the 1MSTS performance in healthy subjects with different morphology.

NCT ID: NCT04715256 Recruiting - Long QT Syndrome Clinical Trials

Evaluation of the Effects of KCNQ1 Mutation on Insulin Tolerance and Obsessive Compulsive Features in Long QT Romano-Ward Syndrome Patients.

PRIME
Start date: January 8, 2021
Phase: N/A
Study type: Interventional

The objectives of the study are to investigate if KCNQ1 mutation in Romano-Ward long QT patients can be associated with changes in insulin regulation and with psychological features of compulsivity, impulsivity and behavioural rigidity.

NCT ID: NCT04513782 Recruiting - Healthy Individuals Clinical Trials

The Contributions of Age Related Changes in the Sound Localization Pathway to Central Hearing Loss

Start date: October 1, 2020
Phase:
Study type: Observational

Age-related hearing loss, presbycusis, affects up to 50% of American adults. There are two main causes for presbycusis: 1) Progressive death of hair cells in the inner ear, and 2) Central hearing loss, or the reduced ability to decipher the sound source of interest from other competing sounds in a multi-source complex environment. The first cause is better understood and treatment options, such as hearing aids and cochlear implants, are available. However, central hearing loss is not as well understood and there is not a treatment available at this time. This study aims to advance our understanding of central hearing loss by evaluating the abilities of younger and older listeners in two primary outcome measures: to 1) neurologically process sound stimuli and 2) focus on conversational speech in the presence of spatially-separated competing background noise. A test using Auditory Brainstem Responses (ABR) will be used to evaluate the brain's response to clicking sounds. This study will assess all waveform data, but will focus particularly on wave III. Sentence in noise tests will be used to assess each subject's ability to process speech in noisy situations. Both the ABR and sentence in noise tests are non-invasive and are commonly used in audiology practices to diagnosis and treat a variety of audiological pathologies.

NCT ID: NCT04466761 Recruiting - Healthy Individuals Clinical Trials

Ascending Glycan Dietary Supplementation in Healthy Adults

Start date: June 23, 2022
Phase: Phase 1
Study type: Interventional

The investigators will conduct a parallel-group, placebo-controlled, randomized, double-blind ascending dose Phase I study of dietary supplementation in healthy individuals to evaluate safety and to determine the pharmacologically effective dose (ED).