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NCT ID: NCT05451186 Completed - Clinical trials for Intensive Care Unit Syndrome

The Eye Patch and Headset on Sleep Quality, Anxiety, Fear and Vital Signs

Start date: June 20, 2022
Phase: N/A
Study type: Interventional

This study was planned to investigate the effects of eye patch and headphones on sleep quality, anxiety, fear and vital signs in coronary intensive care unit patients.

NCT ID: NCT05450926 Completed - Neck Pain Clinical Trials

Selective Cervical Root Block for Chronic Pain

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

Currently, selective cervical nerve root injections are recommended under the guidance of fluoroscopy, ultrasonography and computed tomography in patients with chronic cervical radicular pain who do not respond to conservative treatments and are not planned for surgery. Various serious complications, mainly vascular, have been reported in the literature. These complications include vertebral artery injury, spinal cord and brain stem infarction. The arteries of the cervical spinal cord are the vertebral, ascending, and deep cervical arteries arising from the aorta.The arteries arising from these main arteries and reaching the intervertebral foramen are called segmental arteries, the arteries reaching the epidural region from the intervertebral foramen and the radicular arteries, and the branches reaching the spinal cord are called the medullary artery. These small arteries supplying the spinal cord lie close to the spinal nerve in the foramen between the anterior and posterior trabercules. Vasospasm or embolism, which occurs as a result of direct needle trauma to these vascular structures around the target nerve or injection of particulate steroids, are the most common causes of complication development. The aim of our study is to identify the vascular structures around the foramen in selective cervical root injection, which has proven effectiveness in cervical radicular pain, to determine the most reliable method for positioning the needle while reaching the target nerve under US guidance and to prevent possible complications.

NCT ID: NCT05450666 Completed - Mobility Limitation Clinical Trials

Effectiveness of Mobility Exercises in Resistance-Trained Males With Shoulder Immobility in Different Age Groups

Start date: July 3, 2022
Phase: N/A
Study type: Interventional

The shoulder is a dynamic and mobile joint between the arm and the trunk. The movement of the joint in three dimensions performs complex movements in almost every activity of daily life. These movements performed during activities of daily living can cause musculoskeletal problems and shoulder pathologies. For this reason, the shoulder joint should be carefully evaluated, especially in athletes.

NCT ID: NCT05450510 Recruiting - Rotator Cuff Tears Clinical Trials

Slow and Accelerated Rehabilitation Protocols

Start date: April 27, 2022
Phase: N/A
Study type: Interventional

Latissimus dorsi transfer is an established treatment option with favorable results in massive, irreparable rotator cuff tears, however, it is controversial if earlier motion is detrimental or beneficial to the postoperative goal of reduced pain and improved clinical outcomes. Therefore, the aim of this study is to compare the effects of slow and accelerated rehabilitation protocols after latissimus dorsi transfer in massive, irreparable rotator cuff tears.

NCT ID: NCT05450341 Recruiting - Aphasia Clinical Trials

Efficacy of Low-frequency rTMS in Aphasia

Start date: July 18, 2022
Phase: N/A
Study type: Interventional

In a randomized controlled trial, efficacy of low-frequency, inhibitory rTMS will be examined in rehabilitation of acquired aphasia. Two cortical sites will be targeted: Right-hemispheric homologues of Broca's and Wernicke's areas. In addition to cognitive screening prior to onset of rTMS, language assessments will be conducted before, during and after the intervention. An eyetracking-while-listening experiment will also be conducted before and after the intervention to investigate morphosyntactic processing.

NCT ID: NCT05450211 Completed - Regional Anesthesia Clinical Trials

Evaluation of Postoperative Analgesic Efficacy of Suprainguinal Fascia Iliaca Block

Start date: July 25, 2022
Phase: N/A
Study type: Interventional

It was aimed to evaluate the postoperative analgesic efficacy of the suprainguinal fascia iliaca block applied in the postoperative period in terms of 24-hour opioid consumption, pain score, additional analgesic need, and side effects and complications in the postoperative period, and to see the postoperative analgesic effectiveness of this block in patients who underwent knee arthroplasty.

NCT ID: NCT05450133 Recruiting - Clinical trials for Ankylosing Spondylitis

Hematological Parameters in Axial Spondyloarthritis

Start date: July 15, 2022
Phase:
Study type: Observational

Axial spondyloarthritis is an inflammatory disease characterized by the involvement of the sacroiliac joints and the spine. Disease activity and structural changes are determined by using physical examination, imaging studies, laboratory parameters, and patient-reported indices. Among laboratory studies, Erythrocyte sedimentation rate (ESR) and c-reactive protein (CRP) are the most commonly utilized parameters. However, the level of ESR and CRP are inadequate in demonstrating disease activity and inflammation compared to other diseases. In this study, the investigators aimed to analyze and compare the systemic inflammatory index (SII), which is a hematologic parameter between subjects with radiographic axial spondyloarthritis, non-radiographic axial spondyloarthritis, and healthy controls. Secondarily, the relationship between disease activity and enthesitis score and SII scores in patients with radiographic and non-radiographic axial spondyloarthritis will be investigated.

NCT ID: NCT05449977 Completed - Schizophrenia Clinical Trials

Evaluation of Physical Activity, Physical Fitness, and Quality of Life in Patients With Schizophrenia

Start date: July 6, 2022
Phase:
Study type: Observational

The aim of this study is to evaluate schizophrenic patients who benefit from community mental health center services in terms of physical activity, physical fitness, and quality of life.

NCT ID: NCT05449821 Completed - Obesity Clinical Trials

Investigation of Asprosin a Novel Adipokine in Periodontitis

Start date: January 1, 2022
Phase:
Study type: Observational

Asprosin, a recently discovered glucogenic adipokine, is mainly synthesized by white adipose tissue and released during fasting. Appetite, glucose metabolism, insulin resistance, cell apoptosis, etc. asprosin is associated with diseases such as diabetes, obesity, polycystic ovary syndrome, and cardiovascular diseases. Periodontal tissue may act as a source of endocrine-like inflammatory mediators (such as TNF-α, IL-6 and IL-1) that are important in periodontal inflammation and can affect glucose and lipid metabolism. Production of TNF-α and IL-6 in adipose tissues strengthens the relationship between obesity, T2DM and periodontitis.we postulated that asprosin may be candidate for explaining the triangular relationship among obesity, T2DM, and periodontal disease.

NCT ID: NCT05449626 Completed - Alzheimer Disease Clinical Trials

Validity and Reliability of Turkish Version of Bayer Activities of Daily Living Scale

Start date: July 26, 2022
Phase:
Study type: Observational

The aim of our study is to verify the validity and reliability of the Turkish version of B-GYA.