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NCT ID: NCT06449599 Recruiting - Postoperative Pain Clinical Trials

Rhomboid Intercostal Block in Cardioverter Defibrillator Implantation (ICD)

Start date: June 4, 2024
Phase: N/A
Study type: Interventional

ICD implantation can be painful procedure even under local anesthesia and sedation. In this prospective-randomised study, ultrasound-guided rhomboid intercostal block will be performed to reduce intraoperative and postoperative pain. Also comfort of patients and the cardiologists will be evaluated. In this way, we expect to reduce possible complications and make this procedure more comfortable for patients and clinicians.

NCT ID: NCT06449573 Recruiting - Asthma Clinical Trials

Evaluation of Cardiopulmonary Parameters in Individuals With Asthma

Start date: March 1, 2024
Phase:
Study type: Observational

The aim of the study compare the cardiopulmonary parameters of individuals with asthma with healthy subjects.

NCT ID: NCT06449456 Recruiting - Quality of Life Clinical Trials

Exercise Capacity, Physical Fitness, and Physical Activity Levels in Children With CAH

Start date: February 22, 2024
Phase:
Study type: Observational [Patient Registry]

Congenital Adrenal Hyperplesia (CAH) is a group of automosal recessive disorders that develop due to a deficiency of one of the five enyzmes necessary for cortisol synthesis in the adrenal cortex. Research indicates a predisposition in children and adolescents with CAH towards adverse metabolic changes such as obesity, hypertension, insulin resistance and increased intima-media thickness. This study aims to compare the extent to which children and adolescents with CAH are effected in terms of respiratory and peripheral muscle strength, exercise capasity, physical fitness and physical activity levels compared o their matched healthy individuals.

NCT ID: NCT06449443 Not yet recruiting - Clinical trials for Edentulous Alveolar Ridge

Zero Echo Time MR for the Assessment of Maxillary Sinus and Dental Regions

ZTE-DENTAL
Start date: June 1, 2024
Phase:
Study type: Observational

The aim of this study is to evaluate the efficacy of zero echo time magnetic resonance imaging (ZTE MRI) as an ionizing radiation-free diagnostic method to evaluate both hard and soft tissues and maxillary sinus region before dental implants in the posterior maxillary region.

NCT ID: NCT06449144 Not yet recruiting - Postoperative Pain Clinical Trials

The Effect of Mindfulness Training on Postoperative Pain - A Solomon Four Group Design

Start date: July 1, 2024
Phase: N/A
Study type: Interventional

The goal of this clinical trial is to learn if mindfulness education works to reduce pain after inguinal hernia operation in adults. The main questions it aims to answer are: Does mindfulness education reduce the pain level after inguinal hernia operation? Does mindfulness education reduce the pain intrusion level after inguinal hernia operation? Does mindfulness education reduce the fear of pain level after inguinal hernia operation? Participants will: Pain level, pain intrusion and fear of pain levels will be determined 24 hours before surgery. Awareness training will be given before surgery. Pain level, pain intrusion and fear of pain levels will be determined 24 hours after surgery.

NCT ID: NCT06448377 Recruiting - Airway Management Clinical Trials

Initiation of Airway Code: The Role of the Airway Team in Unexpected Difficult Airways

Start date: March 15, 2024
Phase:
Study type: Observational

The aim of our study is to observationally examine our unexpected difficult airway incidence and intervention times. In addition, it is aimed to discuss the clinical effect of a team specialized in airway intervention intervening in cases by call on the success of airway intervention. In this discussion, it is aimed to use the opinion-opposition method.

NCT ID: NCT06448078 Completed - Trauma Clinical Trials

Comparative Evaluation of External Chest Wall Fixator Treatment Effectiveness in Patients With Rib Fractures

Start date: October 21, 2020
Phase: N/A
Study type: Interventional

This study aimed to investigate the effect of external chest wall fixator on patients' pain level, complication development and hospital stay in patients with rib fractures.Patients who were admitted due to trauma and had serial rib fractures were evaluated. Standard treatment was applied to the control group. External chest wall fixator was applied to the case group in standard treatment. Pain levels of the patients, development of complications and duration of hospitalization were recorded.

NCT ID: NCT06447818 Recruiting - Clinical trials for Obstructive Sleep Apnea of Adult

Changes in Difficult Airway Markers After Surgery for Obstructive Sleep Apnoea Syndrome

Start date: May 15, 2024
Phase:
Study type: Observational [Patient Registry]

This study investigates the changes in difficult airway markers at 6 months post operatively in patients undergoing obstructive sleep apnoea surgery

NCT ID: NCT06447688 Recruiting - Radial Artery Spasm Clinical Trials

Does Verapamil Given Orally Prevent Radial Artery Spasm During Transradial Coronary Angiography

Start date: June 5, 2024
Phase: Phase 4
Study type: Interventional

Coronary angiography (CAG) is an invasive imaging method performed to determine the degree of coronary artery disease. Radial artery spasm (RAS) is one of the most common complications during coronary angiography performed via the transradial approach, causing patient discomfort or sometimes interrupting the procedure. There are many studies on RAS, and various pharmacoagents administered intravenously (intraarterial) to prevent RAS have been described. However, there is limited data in the literature regarding oral pharmacoagents that will prevent this complication. In our study, the preventive effect of Verapamil, given orally 2 hours before coronary angiography, on radial artery spasm will be investigated.

NCT ID: NCT06447649 Completed - Stroke Clinical Trials

Investigation of Factors Affecting Shoulder Pain in Stroke Survivors

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

The aim of this study was to examine the factors affecting shoulder pain in stroke survivors and to determine how much the factors affect shoulder pain