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NCT ID: NCT05833620 Not yet recruiting - Clinical trials for Hereditary Angioedema With C1 Esterase Inhibitor Deficiency

Identification and Characterization of Genetic Variants in Hereditary Angioedema

GENOMAEH_01
Start date: May 2023
Phase:
Study type: Observational

This project aims to analyse in an unbiased way the existence of genetic variants that contribute to explaining and predicting the differences in clinical expression between patients with HAE.

NCT ID: NCT05832593 Not yet recruiting - Clinical trials for Laryngeal Squamous Cell Carcinoma

Immunohistochemical Expression of Excision Repair Cross Complementation Group 1 (ERCC1) in Laryngeal Squamous Cell Carcinoma and Its Correlation With Response to Radiotherapy.

Start date: May 1, 2023
Phase:
Study type: Observational

1. Determine the correlation between immunohistochemical expression of ERCC1 in laryngeal cancer cells with clinico-pathological variables. 2. Assess the correlation between ERCC1 expression and response to radiotherapy.

NCT ID: NCT05830474 Not yet recruiting - Clinical trials for Postoperative Pulmonary Complications

Effect of Continuous Intra-airway Monitoring Under Visible Double-lumen Bronchial Catheter on Postoperative Complications of Lung Surgery

Start date: May 15, 2023
Phase: N/A
Study type: Interventional

The incidence of postoperative pulmonary complications (PPCs) after thoracic surgery is as high as 30-50% [1-6], which is the main cause of postoperative morbidity, death and prolonged hospital stay. Optimization of risk factors in PPCs procedures is the focus of current research. Double lumen bronchial tube (DLT) is a commonly used lung isolation method for adult patients. It has the advantages of good lung isolation effect, sufficient exposure of the surgical field and easy to attract secretions in the airway. However, there are still some deficiencies in clinical precise positioning, long-term continuous detection during operation, early detection of catheter displacement and other emergencies. Continuous intra-airway monitoring is the main advantage of visual double-lumen bronchial catheter. It can quickly and easily determine the position of the catheter and quickly adjust the displacement, and timely and effectively clean up the secretion in the airway, which is conducive to the analysis and treatment of intraoperative hypoxemia. Whether these potential advantages can reduce the incidence of PPCs deserves our in-depth discussion. The research group randomly divided the patients who were scheduled to undergo thoracoscopic radical resection of lung cancer in the Union Hospital affiliated to Fujian Medical University into the test group (lung isolation with visible double-lumen bronchial catheter, continuous intra-airway monitoring and intervention) and the control group: (Pulmonary isolation was performed with visual double-lumen bronchial catheter, and only intra-airway video was performed without monitoring. The effect of continuous intra-airway monitoring under visual double-lumen bronchial catheter on postoperative complications of lung surgery was evaluated by Melbourne evaluation scale.

NCT ID: NCT05829096 Not yet recruiting - Physiotherapy Clinical Trials

The COMBINED Study to Integrate Health Behaviour Change for People With a Rotator Cuff Disorder

COMBINED
Start date: May 1, 2023
Phase: N/A
Study type: Interventional

COMBINED is a pragmatic single-arm feasibility study. The goal of this study is to evaluate the implementation of a physiotherapy-led intervention, The COMBINED approach, to facilitate ongoing refinements, including the strategies for implementation, in readiness for a definitive trial in people with a rotator cuff disorder. The main questions it aims to answer are: 1) What are the key domains of behaviour change influencing the implementation of The COMBINED approach among physiotherapists? 2) Can The COMBINED approach be delivered as intended? 3) Are there any refinements required to the intervention components? 4) What is the patient experience of receiving The COMBINED approach in an NHS setting?

NCT ID: NCT05828888 Not yet recruiting - Clinical trials for Heart Failure With Preserved Ejection Fraction

CHIP in Endothelial Dysfunction Associated With HEpEF

CHiEF
Start date: May 1, 2023
Phase:
Study type: Observational

This study aims at identifying processes that are deregulated in blood cells by Clonal Hematopoiesis of Indeterminate Potential (CHIP) which are involved in the development of heart failure with preserved ejection fraction (HEpEF).

NCT ID: NCT05825495 Not yet recruiting - Pain, Postoperative Clinical Trials

Postoperative Pain Management on Uvulopalatopharyngoplasty Patients

Start date: May 1, 2023
Phase: Phase 4
Study type: Interventional

This is a randomized controlled study, aimed to investigate the effects of dinalbuphine sebacate (DS) on patients having uvulopalatopharyngoplasty (UPPP). DS is a prodrug of nalbuphine, a mixed agonist-antagonist opioid. The mean absorption time for the complete release of DS into systemic circulation is approximately 145 h, which could theoretically provide extended analgesic effects for up to 6 days. Patients diagnosed with obstructive sleep apnea are generally associated with higher risks towards opioid side effects, especially respiratory depression. Post-UPPP pain managing should be cautiously arranged and executed. We hypothesize that the combination of our routine practice and DS will improve the outcomes after Uppp.

NCT ID: NCT05823909 Not yet recruiting - Clinical trials for Respiratory Insufficiency Syndrome of Newborn

A Randomized, Multicenter Study of the Safety and Performance of Fabian PRICO for Saturation Targeting With Non-invasive Respiratory Support

Start date: June 2023
Phase:
Study type: Observational

This study is planned as a part of the post market clinical follow-up (PMCF) on a CE marked product. The purpose of this study is to assess, in a routine clinical environment at two centers the use of fabian-PRICO with noninvasive ventilation and its safety and performance at targeting and maintaining accurate SpO2 levels.

NCT ID: NCT05822700 Not yet recruiting - Clinical trials for Developmental Dysplasia of the Hip

Outcome Of Using Transfixing K Wire ln DDH With Hypoplastic Head And Severe Generalised Ligamentous Laxity

Start date: May 2023
Phase: N/A
Study type: Interventional

This study is to evaluate the outcome of using transfixing hip k wire in Developmental dysplastic hip in patients with hypoplastic head and severe generalised ligamentous laxity.

NCT ID: NCT05822622 Not yet recruiting - Clinical trials for Heart Failure With Preserved Ejection Fraction

Relationship Between Heart Failure With Preserved Ejection Fraction and Nonalcoholic Fatty Liver Disease.

Start date: April 29, 2023
Phase:
Study type: Observational [Patient Registry]

The aim of our study to determine the demography, relation between patients with heart failure with preserved ejection fraction and those with nonalcoholic fatty liver disease in Sohag university hospital.

NCT ID: NCT05817578 Not yet recruiting - Rotator Cuff Tears Clinical Trials

Profiling the RCRSP Patient: a Pain Phenotype Classification Algorithm

Start date: September 2, 2023
Phase:
Study type: Observational

The aim of this study is to collect a sum of different characteristics that have been mentioned previously in people presenting with RCRSP and by clustering them to create a phenotype system which may assist the individualisation of their management