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NCT ID: NCT04344639 Completed - Clinical trials for Necrotizing Enterocolitis

Incidence, Risk Factors, Severity and Prognosis of Necrotizing Enterocolitis in Turkey

Start date: March 1, 2019
Phase:
Study type: Observational

Necrotizing enterocolitis (NEC) is a gastrointestinal system disease characterized by inflammatory necrosis of the intestine mainly seen in premature infants, and continues to be an important cause of mortality and morbidity in neonatal intensive care units all over the world. Although it is more common in premature infants, it is also seen in term babies when the intestine is ischemic. Although the major problem in premature babies is the immaturity of the intestine, many factors contributing to immaturity play a role in the pathogenesis of NEC.

NCT ID: NCT04344392 Completed - Stroke Clinical Trials

Screening of Dysphagia Via Ultrasonography in Patients With Stroke

Start date: January 22, 2022
Phase: N/A
Study type: Interventional

Oropharyngeal dysphagia is commonly seen in patients with stroke. Clinical assessment may be used to evaluate dysphagia in patients with stroke however reliability of this method is controversial and videofluoroscopic study is still considered as gold standard. However, exposure to radiation, necessity for a experienced practitioner, an expensive device, and swallowing contrast agents are disadvantages of videofluoroscopy. Ultrasonography, on the other hand, is a cheap, noninvasive device which may demonstrate tongue and laryngeal movement dynamically. In this manner, this study aims to evaluate whether ultrasound can assess dysphagia in patients with hemiplegia accurately.

NCT ID: NCT04344275 Completed - Clinical trials for Asymptomatic Subjects

The Immediate Effects of Kinesio-Taping on Scapular Muscle Endurance and Strength in Asymptomatic Subjects

Start date: September 15, 2018
Phase: N/A
Study type: Interventional

The purpose of this study was to investigate the immediate effects of Kinesio-taping (KT) on scapular muscle endurance and strength and compared to placebo Kinesio-taping in asymptomatic subjects.

NCT ID: NCT04343937 Completed - Postoperative Pain Clinical Trials

Retrolaminar Block for Postoperative Analgesia in Lumbar Herniectomy Surgery

Start date: April 15, 2020
Phase:
Study type: Observational

This retrospective study included 30 patients scheduled for lumbar herniectomy under general anesthesia. The patients were randomized to receive either retrolaminar block or intravenous analgesia treatment.Numeric Pain Rating Scale (NPRS) was used to measure the pain intensity of patients in postoperative period. Postoperative analgesic requirements were recorded to asses effectiveness of regional anesthesia.Opiod and NSAİD as rescue medication were recorded postoperatively.

NCT ID: NCT04343352 Completed - Epilepsy Clinical Trials

Evaluation of the Efficiency of Mobile Application for Parents of Children With Epilepsy

Start date: October 17, 2020
Phase: N/A
Study type: Interventional

Introduction: support to family and child related to epilepsy, controls or when they come for urgent reasons. Solutions must be found to ensure its continuity. this support. The widespread use of the Internet today, e-health and health education is increasing day by day. Objective: The investigators research is planned to develop a mobile Epilepsy Training Program. Parents with children diagnosed with epilepsy and assessing its effectiveness. Material and Method: The research is a randomized controlled experimental study. An application was made to the Eskişehir Osmangazi University Clinical Research Ethics Committee and the ethics committee permission was obtained with the decision of 13.02.2020 dated 80558721-050.99-E.20230 and 2019-66 decision. Only volunteer participants will be included in the research. Its population study 3-6 years old children diagnosed with epilepsy Eskişehir City Hospital Child Neurology Outpatient Clinic between 01 September 2020 and 31 September 2021. The sample of the research will consist of parents who meet the inclusion criteria. research between these dates. Parents meeting research sample selection criteria The application was randomized as a control group according to the Parent Epilepsy Information Scale. Application group; will use the mobile application the investigators prepared for the parent. Control group will consist of parents who follow the hospital's treatment protocol. The investigators study Completed with a total of 60 parents, 30 of whom are determined by power analysis group. Statistical analysis will be done with SPSS package program. Keywords: Child, Epilepsy, Parent Education, Mobile Application, Child Nurse

NCT ID: NCT04342247 Completed - Clinical trials for Effects of the External Testosteron Intake Over the Choroids of the Patients With Androgen Deficiency

Effects of External Testosteron Intake on the Choroid: Enhance-depth Imaging Optical Coherence Tomography Study

Start date: January 1, 2019
Phase:
Study type: Observational

According to the results Ciloğlu et al., CSC is related to elevated total testosterone levels. Testosterone may play a role in predisposing males to CSC. Thus, we aimed to investigate the possible effect of external testosteron intake over choroidal parameters; such as choroidal thickness, choroidal vascularity index, choroidal stromal ve luminal areas,ect.

NCT ID: NCT04342208 Completed - Clinical trials for Musculoskeletal Pain

Evaluate the Working Environments of Individuals Working From Home During Covid-19 Outbreak

Start date: May 29, 2020
Phase:
Study type: Observational

The study aims to evaluate the working environments of individuals working from home during the covid-19 outbreak and the effect of the working environments on their musculoskeletal system.

NCT ID: NCT04339673 Completed - Local Anesthesia Clinical Trials

Is Masseteric Nerve Block Effective in Myofascial Pain

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

The aim of the present study was to compare the efficacy of three different treatment methods in the management of myofascial pain: masseteric nerve block (MN), trigger point injection(TrP) with local anesthetic (LA) and dry needling (DN).Study Design: 45 subjects aged 18-54 years were randomly assigned to the MN group (n= 15), LA group (n=15) and DN group (n=15).

NCT ID: NCT04339491 Completed - Social Isolation Clinical Trials

Physical Activity During Social Isolation

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

The aim of the study is to evaluate the physical activity level and the factors affecting physical activity among young adults who are socially isolated due to coronavirus.

NCT ID: NCT04339478 Recruiting - Thyroid Cancer Clinical Trials

Does Parathyroid Autofluorescence Reduces Unintensional Parathyroidectomy During Total Thyroidectomy With Central Lymph Node Compartment Dissection

FLUOBCC
Start date: April 6, 2020
Phase:
Study type: Observational

The aim of the study is to evaluate the effectiveness of autofluorescence in the intraoperative preservation of parathyroids during total thyroidectomy with central lymph node compartment dissection.