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NCT ID: NCT04740619 Completed - Mortality Clinical Trials

Natural Orifice Specimen Extraction in Sigmoid Volvulus

Start date: January 1, 2018
Phase:
Study type: Observational

Sigmoid resection can be performed using conventional and laparoscopic methods. There are few publications in the literature reporting specimen removal from the natural hole in patients with a diagnosis of sigmoid volvulus. Here, the investigators aimed to present the literature that transanal specimen removal is a technically feasible method after laparoscopic surgery in patients with sigmoid volvulus.

NCT ID: NCT04740359 Completed - Clinical trials for Ataxia, Spinocerebellar

Functional Trunk Training in Ataxia Patients

Start date: February 12, 2021
Phase: N/A
Study type: Interventional

The study is to examine the effect of functional trunk training on trunk control and upper extremity functions in patients with autosomal recessive ataxia.

NCT ID: NCT04739514 Not yet recruiting - Stroke, Acute Clinical Trials

Development of Dysphagia Protocol in Ankara City Hospital Stroke Patients

Start date: February 1, 2021
Phase: N/A
Study type: Interventional

Stroke, also called cerebrovascular disease, is a sudden-onset neurological disorder that causes a regional or general dysfunction in the brain due to vascular causes. Dysphagia, one of the common complications of stroke, is associated with increased morbidity and mortality.The aim of this study is to evaluate the clinical evaluation of swallowing in stroke patients and to determine the factors affecting the severity and prognosis of dysphagia in patients with dysphagia.Fifty-five patients with acute stroke and dysphagia who were admitted to Ankara City Hospital Neurology Clinic and diagnosed with stroke by neurology and who did not meet the exclusion criteria will be included in this study. When the patients are admitted to the neurology clinic and will be discharged, they will be evaluated three times, in the first month after discharge.

NCT ID: NCT04739488 Completed - COPD Clinical Trials

Breathibg Exercises and Inhaler Trainingfor Chronic Obstructive Pulmonary Disease (COPD) Patients

COPD
Start date: September 10, 2017
Phase: N/A
Study type: Interventional

The most common symptom of chronic obstructive pulmonary disease (COPD) is shortness of breath and causes a decrease in the patient's quality of life. The best way to relieve shortness of breath is inhaler therapy. However, it is known that patients frequently apply this treatment incorrectly. The aim of this study is to determine the effects of breathing exercises and inhaler training for COPD patients on the severity of dyspnea and life quality. For this, two patient groups with a total of 67 people were included in the study. While one group was trained on inhaler drug use, the other group was taught breathing exercises in addition to the inhaler drug use training. Patients were asked to continue the practices they learned regularly for 4 weeks. At the end of the study, it was observed that shortness of breath decreased and the quality of life increased in both patient groups.

NCT ID: NCT04738929 Completed - Obesity Clinical Trials

Comparing EVCO and EVOO

Start date: January 3, 2019
Phase: N/A
Study type: Interventional

The aim of this study is to compare acute effects of consuming extra virgin coconut oil (EVCO) as a source of medium chain fatty acids and extra virgin olive oil (EVOO) as a source of long chain fatty acids in normal weight and obese subjects.

NCT ID: NCT04738916 Completed - Muscle Strength Clinical Trials

Vibration Training in Healthy Individuals

MusMechPro
Start date: January 11, 2020
Phase: N/A
Study type: Interventional

The aim of the study was to examine the effect of six-week constant, low frequency and low amplitude Whole Body Vibration training on the strength and mechanical properties of the lower limb knee extensors and ankle joint dorsi flexor muscles.

NCT ID: NCT04738721 Completed - Assessment, Self Clinical Trials

Physical Activity and Physical Fitness Parameters in COVID-19 Lockdown

Start date: February 5, 2021
Phase:
Study type: Observational [Patient Registry]

In this study; it was aimed to compare the physical activity levels of students who continued their university education face-to-face before the COVID-19 lockdown, and the values of physical activity levels related to health, physical activity levels and health-related physical fitness parameters in the post-lockdown period.

NCT ID: NCT04738500 Not yet recruiting - Postoperative Pain Clinical Trials

Postoperative Analgesic Efficacy of Pericapsular Nerve Group Block (PENG) Block for Knee Arthroscopy

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

Pericapsular nerve group block (PENG) has been deemed as a safe and effective regional technique for postoperative pain after knee arthroscopy.

NCT ID: NCT04738487 Recruiting - Lung Neoplasms Clinical Trials

Coformulation of Pembrolizumab/Vibostolimab (MK-7684A) Versus Pembrolizumab (MK-3475) Monotherapy for Programmed Cell Death 1 Ligand 1 (PD-L1) Positive Metastatic Non-Small Cell Lung Cancer (MK-7684A-003, KEYVIBE-003)

Start date: April 7, 2021
Phase: Phase 3
Study type: Interventional

The primary hypotheses are that coformulated pembrolizumab/vibostolimab is superior to pembrolizumab alone with respect to (1) overall survival (OS) in participants with programmed cell death 1 ligand 1 (PD-L1) tumor proportion score (TPS) ≥50%, TPS ≥1% and TPS 1% to 49%; and (2) progression-free survival (PFS) per Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 by blinded independent central review (BICR), in participants with PD-L1 TPS ≥1% and TPS ≥50%.

NCT ID: NCT04738461 Withdrawn - Clinical trials for Subacromial Pain Syndrome

The Effectiveness of Telerehabilitation in Patients With Subacromial Pain Syndrome

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

The main hypothesis of the study is that telerehabilitation is an effective treatment method and it is not inferior than standard physiotherapy.The aim of this study is to evaluate the effectiveness of telerehabilitation in patients with subacromial pain syndrome by comparing it with standard physiotherapy.