Clinical Trials Logo

Filter by:
NCT ID: NCT05388799 Completed - Nursing Caries Clinical Trials

The Effect of Brochure-Based Education on Patients Planned for Nose Surgery

Start date: August 1, 2022
Phase: N/A
Study type: Interventional

The study was planned as a randomized controlled trial to determine the effect of brochure-based education on fear and anxiety in patients scheduled for nose surgery.It is planned to collect research data in Hatay Mustafa Kemal University Hospital otorhinolaryngology clinic between June 2022 and June 2023.The population of the research will be the patients who are hospitalized in the otorhinolaryngology clinic of the aforementioned hospital and are planned for nasal surgery. The sample of the study, on the other hand, will consist of 52 patients who meet the inclusion criteria and agree to participate in the study verbally and in writing.The data of the study were collected by using the Personal Information Form, the Surgical Fear Scale and the Surgical Anxiety Scale, which were prepared in line with the literature.The data will be analyzed with the SPSS package program.

NCT ID: NCT05388669 Active, not recruiting - Clinical trials for Advanced or Metastatic Non-small Cell Lung Cancer

A Study of Lazertinib With Subcutaneous Amivantamab Compared With Intravenous Amivantamab in Participants With Epidermal Growth Factor Receptor (EGFR)-Mutated Advanced or Metastatic Non-small Cell Lung Cancer

PALOMA-3
Start date: August 5, 2022
Phase: Phase 3
Study type: Interventional

The purpose of the study is to simplify amivantamab intravenous administration and to reduce dose times, by assessing a new formulation of amivantamab, amivantamab subcutaneous and co-formulated with recombinant human hyaluronidase (SC-CF), for subcutaneous administration. This formulation has the potential to enhance both the patient and physician experience with amivantamab by providing easier and accelerated administration.

NCT ID: NCT05388292 Completed - Emergencies Clinical Trials

Decision Support System on Emergency Triage

Start date: July 16, 2020
Phase: N/A
Study type: Interventional

The objective of this study is to design a computer-based Decision Support System (DSS) using the ESI (Emergency Severity Index) and ATS (Australasian Triage Scale) algorithms, integrate it into the Hospital Information Management System (HIMS), evaluate the effect of the triage management in the emergency department and ensure the continuity of the system.

NCT ID: NCT05387824 Recruiting - Clinical trials for Idiopathic Overactive Bladder

Tibial Nerve and Extracorporeal Magnetic Stimulation for Overactive Bladder

Start date: June 2, 2022
Phase: N/A
Study type: Interventional

Overactive bladder (OAB) syndrome is urinary urgency, usually accompanied by frequency and nocturia, with or without urgency urinary incontinence, in the absence of urinary tract infection. For the treatment of OAB; pharmacological and non-pharmacological methods are available. The availability and the continuation rate of pharmacological treatments are lower than non-pharmacological treatments due to side effects. Non-pharmacologic treatment methods are evaluated in two groups as active and passive methods. Active methods which active participation of the patient is required during treatment are Pelvic floor muscle exercise (PFME), biofeedback assisted PFME, vaginal cones, while passive methods are Electrical Stimulation, extracorporeal Magnetic Stimulation (MStim) and Transcutaneous Tibial Nerve Stimulation (TTNS) techniques. In this study, investigators aim to evaluate the effectiveness of TTNS and extracorporeal MStim, which are noninvasive methods, added to bladder training (BT) in women with OAB, with a prospective randomized controlled research method.

NCT ID: NCT05387629 Completed - Nursing Caries Clinical Trials

The Effect of Social Media in Improving the Academic Achievement

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

In today's living conditions, technology is present in every aspect of our lives and is constantly changing and developing. Thanks to technological developments, progress has been made in the field of communication as well as in many other fields, and this has provided the opportunity to access information quickly. Especially the widespread use of mobile phones has facilitated communication. Thanks to smartphones, which are an integral part of daily life, we can quickly access or share information. Especially with smart phones, interactive access is provided through Social Media, which is one of the most advanced communication tools of our age. Commonly used social media tools are Social Networking websites (Facebook, Twitter, Instagram) in our country and around the world. Social media tools have many features for the development of educational processes. Social media can be used in educational processes to improve communication skills of students and teachers, expand participation, strengthen peer support, and realize cooperative learning. Social media teaching processes; It also provides opportunities such as supporting the learning process of students by enriching it with materials such as pictures, text, video, audio, and supporting the teacher's teaching and evaluation process. The purpose of this research; To evaluate the effect of social media in improving the academic success of nursing students.

NCT ID: NCT05387356 Recruiting - Clinical trials for Acute Respiratory Distress Syndrome

Evaluation of the Efficiency and Complications of the Consequtive Proning in Covid -19 ICU

Start date: May 23, 2022
Phase:
Study type: Observational

Thirty -one confirmed Severe Acute Respiratory Syndrome CoronaVirus 2 (SARS-CoV-2 ) infected patients with Acute Respiratory Distress Syndrome (ARDS) and placed in prone position(PP) for 3 times (PP1, PP2, PP3)consecutively will be included. Arterial blood gases (ABG), partial pressure of arterial oxygen/ fraction of inspired oxygen (PaO2/FiO2 ) ratios, partial pressure of carbondioxide (PaCO2), positive end expiratory pressure (PEEP), and fraction of inspired oxygen (FiO2) values will be recorded before (bPP), during (dPP)and after (aPP) every prone positioning. Eye, skin, nerve and tube complications related to prone positions wll be recorded

NCT ID: NCT05386667 Completed - Pain, Postoperative Clinical Trials

Evaluation of the Effects of Medicaments Used After Free Gingival Graft on Postoperative Complications.

Start date: March 5, 2019
Phase:
Study type: Observational [Patient Registry]

In our study, three different medicaments were evaluated in terms of postoperative complications after free gingival grafting (FGG).

NCT ID: NCT05386641 Not yet recruiting - Clinical trials for Breast Cancer Survivors

Risk Factors for Shoulder Joint Motion Restriction

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

In breast cancer patients, limitation of shoulder joint movement may occur following cancer treatment. Shoulder limitation causes a significant decrease in the patient's participation in activities of daily living. The aim of the study is to define these limitations, to evaluate in detail all the structures that cause the problem, and to determine the causes of the limitations in patients with shoulder joint movement limitation developed after breast cancer survivors.

NCT ID: NCT05386628 Not yet recruiting - Clinical trials for Breast Cancer Survivors

The Effect of Myofascial Chain Release Techniques on Shoulder Joint Range of Motion in Breast Cancer Survivors

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

In breast cancer patients, limitation of shoulder joint movement occurs following mastectomy surgery. Studies have reported that damage to the fascia on the pectoralis major muscle during mastectomy surgery contributes to the development of the limitation. The aim of this study is to investigate the effect of release techniques applied to the fascia on the pectoralis major muscle and the fascial chain on the incerasing of shoulder joint range of motion.

NCT ID: NCT05386108 Recruiting - Neoplasms Clinical Trials

Study of Abemaciclib and Elacestrant in Patients With Brain Metastasis Due to HR+/HER2- Breast Cancer

ELECTRA
Start date: August 31, 2022
Phase: Phase 1/Phase 2
Study type: Interventional

This is a multi-site, global, open-label study that includes a phase 1b evaluation of elacestrant in combination with abemaciclib in women and men with with or without brain metastases from ER-positive, HER-2 negative breast cancer. Phase 1b is designed to select the recommended phase 2 dose and will be followed by a phase 2 evaluation of elacestrant in combination with abemaciclib in patients with active brain metastases from ER-positive, HER-2 negative breast cancer.