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NCT ID: NCT04384133 Active, not recruiting - COPD Clinical Trials

The Prevalence of Small Airways Dysfunction In COPD Patients and The Impact on COPD Control

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

Chronic obstructive pulmonary disease (COPD) is a worldwide prevalent disease. During recent years, increasing attention has been directed to the importance of the contribution of small airways in respiratory diseases. The small airways (usually defined as those with an internal diameter of <2 mm) are recognized as the major site of resistance to airflow in obstructive lung disease. Although small airway disease is known in chronic airway diseases, the importance of small airway dysfunction on disease control, exacerbations and quality of life, and the importance of taking place among treatable targets is not clear. Therefore, our aim in the study is to determine the frequency of small airway dysfunction in COPD. Our secondary aim is to evaluate the role of small airway dysfunction in disease severity, disease phenotypes, disease control, quality of life and its effect on predicting the risk of exacerbation and its role among treatable targets in chronic airway diseases.

NCT ID: NCT04383561 Completed - Inflammation Clinical Trials

Relationship Between LRG and Periodontal Disease

Start date: September 30, 2019
Phase: N/A
Study type: Interventional

This study aimed to investigate gingival crevicular fluid (GCF) and serum levels of LRG, interleukin (IL)-6 and tumor necrosis factor (TNF)-α in patients with periodontitis before and after non-surgical periodontal treatment.

NCT ID: NCT04383483 Recruiting - Clinical trials for Coronavirus as the Cause of Diseases Classified Elsewhere

CoV-ICU Score, Intensive Care Unit, SARS-CoV-2

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

In the course of COVID disease, some patients need intensive care treatment. We aim to find an answer to the question of whether the patient's CRP, ferritin, D-dimer, Oxygen Saturation, lymphocyte count, and body mass index can be used as a criterion for admitting patients with COVID to the intensive see unit.

NCT ID: NCT04383249 Completed - Pathology Clinical Trials

Routine Pathological Examination of Hernia Sac; Is it a Workload or Necessary?

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

Routine microscopic examination of the hernia sac is controversial. While some centers do not recommend a routine microscopic examination in inguinal hernias in adult patients, they recommend them in abdominal wall hernias. The investigators aimed to discuss the pathology results and unexpected histopathological findings who underwent abdominal wall and inguinal hernia operation in the light of the literature.

NCT ID: NCT04383132 Completed - Clinical trials for Performance and Tolerance of Colonoscopy

Effectiveness of Abdominal Binder Use During Colonoscopy

Start date: May 15, 2020
Phase: N/A
Study type: Interventional

Colonoscopy is considered the primary screening test for colorectal cancer screening worldwide. For technical difficulties previously experienced during colonoscopy, especially loop of the colonoscopy device in the colon, many solution methods have been developed and applied (manual pressure and position change, etc.). Although these methods are partially successful, there is no consensus on the optimum solution method. Few studies in the literature have investigated the use of corset during colonoscopy and conflicting results have been reported. In this study, elastic abdominal corset or false corset will be used during colonoscopy. Indeed, the investigators aim to determine whether this method is effective and safe with their own results and contribute to the literature. The primary outcome of this study will be the cecal intubation time. Secondary outcomes include manual pressure and position change during the procedure, length of cecal intubation (length of colonoscope required to reach the cecum from the anus), colonoscopy completion rate, additional anesthesia and / or analgesic requirement, patient pain and comfort level and colonoscopic findings.Efficacy will be assessed on the basis of pairwise comparisons between groups with respect to primary and secondary outcomes.

NCT ID: NCT04380636 Active, not recruiting - Clinical trials for Carcinoma, Non-Small-Cell Lung

Study of Pembrolizumab With Concurrent Chemoradiation Therapy Followed by Pembrolizumab With or Without Olaparib in Stage III Non-Small Cell Lung Cancer (NSCLC) (MK-7339-012/KEYLYNK-012)

Start date: July 6, 2020
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess the efficacy and safety of pembrolizumab in combination with concurrent chemoradiation therapy followed by either pembrolizumab with olaparib placebo (Arm 1) or with olaparib (Arm 2) compared to concurrent chemoradiation therapy followed by durvalumab (Arm 3) in participants with unresectable, locally advanced NSCLC. Arms 1 and 2 will be studied in a double-blind design and Arm 3 will be open-label. The primary hypotheses are: 1. Pembrolizumab with concurrent chemoradiation therapy followed by pembrolizumab with olaparib is superior to concurrent chemoradiation therapy followed by durvalumab with respect to progression-free survival (PFS) and overall survival (OS) 2. Pembrolizumab with concurrent chemoradiation therapy followed by pembrolizumab is superior to concurrent chemoradiation therapy followed by durvalumab with respect to PFS and OS

NCT ID: NCT04380272 Completed - Clinical trials for Obstructive Tonsillar Hypertrophy

Development of an Assessment Method for Obstructive Tonsillar Hypertrophy in Children by Ultrasonography

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

Chronic tonsillar hypertrophy is one of the most common causes of upper airway obstruction in children. Currently, several clinical staging systems are used to evaluate airway obstruction due to tonsillar hypertrophy. However, as these staging systems are based on a physical examination, it is not always possible to accurately evaluate the tonsil size, especially in children, and so objective and reliable methods are required in this field. In this study, the investigators aimed to develop a new method for the objective evaluation of airway obstruction due to tonsillar hypertrophy using submental ultrasonography (US) in children.

NCT ID: NCT04379804 Completed - Clinical trials for Recurrent Laryngeal Nerve Injuries

CRANIO-CAUDAL AND LATERAL APPROACH FOR RECURRENT LARYNGEAL NERVE

Start date: June 1, 2018
Phase: N/A
Study type: Interventional

The recurrent laryngeal nerve (RLN) dissection should be performed cranio-caudally in TOETVA approach.The aim of this study was to compare the cranio-caudal and lateral approach for RLN dissection in regard with the rates of LOS during conventional thyroidectomy using continuous intraoperative nerve monitoring (CIONM).

NCT ID: NCT04379765 Completed - Clinical trials for Lumbar Spinal Stenosis

Long-term Follow-up of Conservative and Surgical Treatment Results of Patients With Lumbar Spinal Stenosis

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

Total of 60 patients with a diagnosis of spinal stenosis is planned for 30 patients, with physical therapy modeling and exercise, and 30 patients with surgical treatment. Patients will be evaluated by the same physician 5 times, before early primary treatment, 1st month, 3rd month, 6th month and 12th month after treatment.

NCT ID: NCT04379674 Completed - KINESIOTAPING Clinical Trials

Effect of Kinesiotaping in Different Directions on Muscle

Start date: May 2, 2019
Phase: N/A
Study type: Interventional

The study was conducted to investigate the effects of different Kinesio taping directions on dynamic muscle endurance. This randomized, double-blind, crossover study was implemented on 27 healthy male subjects. Before the study, personal and demographic information of the volunteers were recorded and muscle strength was evaluated in the biceps curl position with 1 maximum repetition technique. One week after this first evaluation muscle endurance was evaluated by counting the accurate elbow flexions completed in biceps curl position with 80% weight of 1 maximum repetition recorded in the first evaluation. Following this second evaluation facilitation, inhibition, and placebo tapings were applied to all the 27 subjects who were randomly assigned into 3 groups sequentially with an interval of two days. The sequence of taping technique to be used for the groups were also randomly determined and applied to the M. Biceps Brachii and muscle endurance was evaluated with the same method half-hour after the tape was applied. All the evaluations were performed by the same evaluator who was blind to the taping technique.