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NCT ID: NCT05185167 Completed - Anesthesia Clinical Trials

Comparison of the Genotoxicity of Desflurane and Propofol

Start date: January 17, 2022
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate if the anesthetics propofol and desflurane can damage DNA according to comet essay in patients submitted to lumbar disc surgery.

NCT ID: NCT05185050 Completed - Clinical trials for Myofascial Pain Syndrome

Prevalence of Myofascial Pain Syndrome in Adolescent Idiopathic Scoliosis

Start date: October 10, 2021
Phase:
Study type: Observational [Patient Registry]

this is an observational and cross-sectional prevalence study. 10-18 years aged participants with adolescent idiopathic scoliosis were recruited in the study. Myofascial pain syndrome will be questioned to the participants. additionally, all participants will be evaluated using their findings for scoliosis and myofascial pain syndrome diagnostic criteria. Cobb angle, coronal balance, shoulder and pelvis asymmetry, sagittal spino-pelvic parameters of the spine (cervical lordosis, thoracic kyphosis, lumbar lordosis angles and sagittal vertical axis, sacral slop angle and pelvic incidence) will be measured.

NCT ID: NCT05184634 Completed - Metabolic Syndrome Clinical Trials

Determination Physical Activity Levels,Quality Life,Depression and Fatigue Severity Individuals With Metabolic Syndrome

Start date: December 15, 2021
Phase: N/A
Study type: Interventional

The aim of the study was to determine the Physical Activity Levels, Quality of Life, Depression and Fatigue Severity of Individuals with Metabolic Syndrome. International Physical Activity Questionnaire (IPAQ) to evaluate the physical activity level of individuals diagnosed with Metabolic Syndrome, to evaluate their quality of life SF-36 will be used to determine depression levels, Beck Depression Scale, and Fatigue Severity Scale (FSS) will be used to evaluate fatigue severity.

NCT ID: NCT05184543 Completed - Sport Injury Clinical Trials

Effects of Different Exercise Programs on Injury Risk and Sports Performance in Adolescent Basketball Players

Start date: January 15, 2022
Phase: N/A
Study type: Interventional

Basketball is a team sport where aerobic and anaerobic performance is important. Knowing how to reduce common injuries and risk is important when designing a warm-up exercise program for basketball. Various warm-up programs, including neuromuscular training, are thought to reduce the incidence of lower extremity injuries and improve athletic performance in athletes. There are several neuromuscular training programs designed to improve joint position sense, increase joint stability, develop protective joint reflexes, and ultimately prevent lower extremity injuries. In the literature, there is a need for studies comparing the effects of various warm-up programs applied to adolescent licensed basketball players on injury risks and basketball-specific sportive performance parameters. Therefore, the aim of the study is to examine the effects of different exercise programs on injury risk and sportive performance in adolescent basketball players.

NCT ID: NCT05184309 Completed - Rehabilitation Clinical Trials

Effects of Serious Games for Shoulder Rehabilitation

Start date: January 10, 2022
Phase: N/A
Study type: Interventional

The aim of this study is to examine the effect of Serious-Game Exercise (SGE) platform on pain, range of motion (ROM), joint position sense, shoulder functions, and approximation force in patients with rotator cuff rupture. In addition, another objective is to evaluate the usage of balance board as a measurement tool for measuring the approximation force in the rotator cuff rupture.

NCT ID: NCT05184244 Completed - Cerebral Palsy Clinical Trials

Turkish Adaptation of the Activity Limitations in Cerebral Palsy Questionnaire

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

This study aimed to make the Turkish adaptation of ACTIVLIM-CP and to examine its psychometric properties. Eighty-nine individuals with CP, aged between 2-18 years were included in the study. PEDİ, ABILOCO-Kids, and ABILHAND-Kids scores and Wee-FIM questionnaires were used for validity analysis. Test re-test method was used for reliability.

NCT ID: NCT05183659 Completed - Muscular Tone Clinical Trials

The Reliability of Myotonometer in Evaluating the Muscle Tone and Biomechanical Properties of the Forearm Muscles

Start date: November 27, 2021
Phase:
Study type: Observational

The primary aim of this study was to evaluate the intra-rater and inter-rater reliability of MyotonPRO in measuring muscle tone and mechanical properties of the wrist extensor and flexor muscles in healthy young adults. The secondary aim is to examine whether grip strength has any effect on muscle tone and biomechanical properties.

NCT ID: NCT05182840 Completed - Clinical trials for Kidney Disease, Chronic

A Study to Test Whether Different Doses of BI 690517 Alone or in Combination With Empagliflozin Improve Kidney Function in People With Chronic Kidney Disease

Start date: January 11, 2022
Phase: Phase 2
Study type: Interventional

This study is open to adults with chronic kidney disease. People with and without type 2 diabetes can take part in this study. The purpose of this study is to find out whether a medicine called BI 690517 improves kidney function in people with chronic kidney disease when taken alone or in combination with a medicine called empagliflozin. In the first part of the study, participants take empagliflozin or placebo as tablets every day for 2 months. Placebo tablets look like empagliflozin tablets but do not contain any medicine. In the second part, participants are divided into several groups. Depending on the group, the participants then additionally take different doses of BI 690517 or placebo as tablets for 3.5 months. In this case, placebo tablets look like BI 690517 tablets but do not contain any medicine. Participants are in the study for about 6 months. During this time, they visit the study site about 12 times. Where possible, about 4 of the 12 visits can be done at the participant's home instead of the study site. The trial staff may also contact the participants by phone or video call. Participants collect urine samples at home. These samples are then analysed to assess kidney function. At the end of the trial the results are compared between the different groups. The doctors also regularly check participants' health and take note of any unwanted effects.

NCT ID: NCT05182671 Completed - Clinical trials for Bladder and Bowel Dysfunction, Hip Strength Ratios

Relationship Between Pelvic Angle, Femoral Anteversion, and Hip Muscle Strength Ratios in Bladder-bowel Dysfunction

Start date: January 15, 2022
Phase:
Study type: Observational [Patient Registry]

Bladder and bowel dysfunction is a combination of lower urinary tract and bowel dysfunction seen in children over 5 years of age without identifiable or discernible neurological abnormalities. The proper functioning of the bladder, bowel, nerves, pelvic floor muscles and related anatomical structures provides the bowel and lower urinary tract function. Dysfunction of any structure of the pelvic floor can potentially cause to bladder and bowel dysfunction. The ability of the pelvic floor muscles to perform the correct contraction and relaxation function is also closely related to the position of the pelvis, muscle strength of the hip muscles, and femoral anteversion. Disruption of one of the links forming the chain causes a change in the mobility and stability of all mechanically related structures and may affect the optimal force that the pelvic floor muscles can produce. As far as investigators know, there is no study in the literature examining the relationship between BBD and pelvic angle, femoral anteversion angle, femoral internal/external rotation angle ratio and hip muscle strength ratios in children with bladder-bowel dysfunction. Considering the close relationship between pelvis position, hip muscle strength, and femoral anteversion with the pelvic floor, investigators think that this relationship should be evaluated in children with BBD and will contribute to the literature.

NCT ID: NCT05182411 Completed - Stroke Clinical Trials

Validity and Reliability of Turkish Version Leg Activity Measure

Start date: June 30, 2022
Phase:
Study type: Observational [Patient Registry]

Patient-filled scales minimize the burden of data collection for clinicians in a clinical setting. Therefore, Leg activity measure, a new self-report measure of active and passive function in the leg, has been developed. Leg activity measure consists of three parts. The first part includes passive functions, the second part includes active functions, and the third part includes the assessment of quality of life. It is a valid and reliable test in adult neurological patients with lower extremity spasticity. It can be used in the evaluation of the active and passive functions of the results of the clinicians' interventions by making the cultural adaptation of the Turkish language and examining its validity and reliability. We think that it will be important to determine the limitations in activity, participation and daily living activities and to evaluate their reflections.