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NCT ID: NCT05432219 Not yet recruiting - Clinical trials for Recurrent Nasopharyngeal Carcinoma

A Transoral Retropterygoid Approach to Resect Recurrent Nasopharyngeal Carcinoma

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

This is a a prospective, single-arm, and exploratory study of endoscopic resection of recurrent nasopharyngeal carcinoma via transoral retropterygoid approach.

NCT ID: NCT05431790 Not yet recruiting - Clinical trials for Anterior Cruciate Ligament Rupture

Absorbable Interface Screw Clinical Trial

Start date: July 30, 2022
Phase: N/A
Study type: Interventional

Validation of the safety and efficacy of absorbable interface screws for clinical use

NCT ID: NCT05431309 Not yet recruiting - Clinical trials for Cardiovascular Primary Prevention Strategy

Role of Screening With Coronary Computed Tomography Angiography in Primary Prevention of Coronary Heart Disease

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

The primary objective of this study is to determine whether coronary computed tomography angiography (CCTA) -based coronary heart disease(CHD) prevention strategy will be superior to traditional CHD prevention strategy, in reducing the future risk of CHD which included myocardial infarction, angina, cardiac death, and an emergency/urgent coronary revascularisation procedure, in a community population aged 40 to 69 years with cardiovascular risk factors but no history of cardiovascular disease.

NCT ID: NCT05430425 Not yet recruiting - Clinical trials for Airway Complication of Anesthesia

Comparison of the Efficiency of Classical and I-GEL LMAs Selected by Different Methods in Providing a Safe Airway

Start date: June 22, 2022
Phase:
Study type: Observational

In recent years, the use of laryngeal masks has been increasing in operating room and non-operating room anesthesia applications. Patients with inappropriate LMA may develop high leakages, gastric distension and inadequate ventilation during ventilation. If the laryngeal masks used to provide a safe airway in the patient are not selected in the appropriate size, adequate ventilation may not be provided, which may lead to various complications such as increased morbidity and mortality. In order to prevent and predict the bad results that may occur, we foresee which method can be chosen more appropriately for the patients and will guide the clinicians.

NCT ID: NCT05427747 Not yet recruiting - Clinical trials for Spontaneous Bacterial Peritonitis

Meropenem vs Cefotaxime as Empirical Treatment of SBP

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

We aimed to evaluate whether meropenem is superior to cefotaxime for treatment of SBP empirically.

NCT ID: NCT05427695 Not yet recruiting - Clinical trials for Chronic Rhinosinusitis (Diagnosis)

Topical Probiotic Sinus Irrigations for Treating Chronic Sinusitis

Start date: June 1, 2024
Phase: Phase 2
Study type: Interventional

The purpose of this randomized study will be to determine whether topical probiotic sinus irrigations are more effective compared to saline sinus irrigation controls in the treatment of active CRS in patients who have had prior sinus surgery based on subjective and objective outcome measures.

NCT ID: NCT05426278 Not yet recruiting - Clinical trials for Nausea and Vomiting, Postoperative

The Effect Of Intraoperative Forced Air Warmer Use, On Postoperative Nausea And Vomiting

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

Intraoperative Hypothermia is a common problem, our object will be to evaluate the efficacy of forced air warmer (Model # eq-5000) for maintaining core body temperature in patients undergoing laparoscopic surgeries and its effect on postoperative nausea, vomiting and shivering.

NCT ID: NCT05425758 Not yet recruiting - Clinical trials for Pediatric Distal Forearm Fractures

Optimal Index for Pediatric Distal Forearm Fractures

Start date: July 1, 2022
Phase:
Study type: Observational

This is a prospective radiographic study of displaced distal forearm fractures requiring manipulation for children 3-12 years of age and will be treated with casting.The patients' full radiographic series (including the pre-manipulation, immediate post-manipulation, after 1 week and after 4 weeks radiographs) will be evaluated.

NCT ID: NCT05424302 Not yet recruiting - Clinical trials for Benign Paroxysmal Positional Vertigo

Effect of Peripheral Vestibular Disease Location on Outcomes Following Home-based Virtual Reality Vestibular Therapy

VR-PVD-RCT
Start date: January 2023
Phase: N/A
Study type: Interventional

This parallel-group randomized controlled trial aims to determine if the location of the lesion(s) in the vestibular system (unilateral versus bilateral, lateral semi-circular canal versus otolith) impacts the effectiveness of adjunct take-home head-mounted display (HMD) virtual reality (VR) therapy in improving patient symptomatology. Fifty patients meeting inclusion criteria will be recruited from the principal investigator's neurotology clinic. Baseline symptomatology questionnaires will be completed, followed by random allocation to virtual reality and control groups. Vestibular rehabilitation and virtual reality protocols will be adhered to for 4 to 8 weeks, followed by symptomatology questionnaires. Data analysis will be conducted to answer the study's objectives.

NCT ID: NCT05423197 Not yet recruiting - Clinical trials for Head-and-neck Squamous Cell Carcinoma

Study Evaluating Zr-Panitumumab for Assessment of Suspected Metastatic Lesions on 18F-FDG-PET/CT in Head and Neck Squamous Cell Carcinoma

Start date: June 2024
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the diagnostic utility of 89Zr-panitumumab to identify metastatic lesion(s) in subjects with head and neck squamous cell carcinoma (HNSCC).