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Diagnoses Disease clinical trials

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NCT ID: NCT04858919 Completed - Diagnoses Disease Clinical Trials

Transrectal and 3D Transabdominal Ultrasound Compared to Vaginoscopy in Diagnosing Virgins With Genital Lesions

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

This study is to compare the feasibility and test performance of different 3D pelvic ultrasound and Transrectal ultrasound in the detection of local lesions in the uterus , cervix and vagina compared to the final diagnosis confirmed by vaginoscopy as a golden standard modality of diagnosis in Virgin Patients

NCT ID: NCT04843878 Completed - Coronavirus Clinical Trials

COVID-19 Testing Pilot Study

Start date: January 5, 2021
Phase:
Study type: Observational

The purpose of this study is to determine the reliability of a low-cost rapid diagnostic test for COVID-19. The method of the testing procedure uses electrochemistry to detect COVID-19 spike proteins within human samples. To test the effectiveness of this new method, patients will be recruited as they present for testing at ambulatory Penn testing sites. Patients will be asked to self-collect one anterior nares samples under the supervision of authorized study personnel.

NCT ID: NCT04788966 Completed - Diagnoses Disease Clinical Trials

Evaluation of an Innovative Speech-enabled Translator in Emergency Settings

Start date: November 29, 2018
Phase:
Study type: Observational

Survey-based satisfaction, performance and technical features evaluation of a speech-enabled fixed-phrase translation tool (BabelDR) in an emergency department.

NCT ID: NCT04743843 Completed - Diagnoses Disease Clinical Trials

Concordance Between Omnyx System With Omnyx .RTS Images and the Omnyx Dynamyx Software With Hamamatsu .NDPI Images

Start date: January 22, 2019
Phase:
Study type: Observational

This study serves as a validation study for the Omnyx Dynamyx software and Hamamatsu .ndpi image file format, evaluating agreement of diagnosis between whole slide images (WSI) of the Omnyx system (Omnyx scanned .rts images and Omnyx Dynamyx software) and the Omnyx Dynamyx software with the Hamamatsu .ndpi images. The primary goal of this study is to demonstrate concordance between the two systems to validate the Omnyx Dynamyx software with the non-Omnyx .ndpi image file type.

NCT ID: NCT04689126 Completed - Diagnoses Disease Clinical Trials

Effect of Cone Beam Computed Tomography on Diagnostic and Therapeutic Decision Making

Start date: November 1, 2016
Phase: N/A
Study type: Interventional

this study will determine the effect of CBCT examinations on diagnostic and therapeutic decision making in endodontics.

NCT ID: NCT04688463 Completed - Appendicitis Clinical Trials

Evaluation of Pressure Algometry in the Clinical Assessment of Acute Abdominal Pain in Children

Start date: January 1, 2000
Phase:
Study type: Observational

In this retrospective observational case study, the investigators review the clinical experience with pressure-pain algometry in children with suspected appendicitis. The investigators hypothesized that algometry can discriminate children with appendicitis from children without appendicitis and aimed to determine the diagnostic accuracy of algometry, compared to ultrasound imaging and clinical assessment.

NCT ID: NCT04662853 Active, not recruiting - Cancer Clinical Trials

Gut Microbiota and Color-rectal Cancer.

CCR-microbiota
Start date: January 17, 2017
Phase:
Study type: Observational [Patient Registry]

This clinical trial is focused in the development of a screening test for the people at risk of colo-rectal cancer (aged more than 50 years old), valid and safe, improving the screening prognosis increasing the sensitivity and sensitive as compared with the current method, fecal occult blood.

NCT ID: NCT04659265 Completed - Diagnoses Disease Clinical Trials

A Priori Diagnosis and Diagnostic Errors

Start date: January 2011
Phase: N/A
Study type: Interventional

This is a prospective randomized single-blind simulator-based trial. 156 4th year medical students were randomised to receive one of three different suspected diagnoses of a pre-treating physician (no diagnosis, myocardial infarction, pulmonary embolism) prior to the task to make a focussed assessment and perform first management steps in a patient presenting to the emergency department. The patient (simulator) suffered from an acute myocardial infarction. Video recordings were obtained during simulation and used for data analysis. Primary endpoint was the participants' final presuptive diagnosis.

NCT ID: NCT04652141 Recruiting - Asthma Clinical Trials

Asthma Diagnosis Verified by Lung Function

ADVERT
Start date: December 1, 2020
Phase: N/A
Study type: Interventional

Guidelines suggests that asthma should not be treated prior to a reversibility test and/or an assessment with peak expiratory flow (PEF) unless there is a clinical urgency for the patient to be treated. Approximately one third of patients with diagnosed asthma can safely step-wise withdraw their asthma medication and diagnosis based on repeated objective lung function measurements. AsthmaTuner is CE-marked and provides doctors and nurses with information on patient spirometry incl. reversibility test and diurnal or weekly variability of PEF in relation perceived symptoms. Thereby, digital supported asthma care with AsthmaTuner can improve objective diagnosis of asthma. The objectives of this study are to evaluate the sensitivity and specificity to establish objective asthma diagnosis with spirometry including reversibility test and PEF-monitoring with AsthmaTuner, and secondary, assess the number of asthma patients with objective verified asthma diagnosis with use of spirometry including reversibility test and/or periodic variability with PEF/FEV1 between traditional trial treatment and treatment with AsthmaTuner. At least 146 patients will be included who are at least six years old, with respiratory symptoms that can be signed to asthma last month or with physician-diagnosed asthma last five years without intake of anti-inflammatory treatment in the last three months. This is a randomised controlled trial evaluating a diagnostic two step algorithm that firstly includes dynamic spirometry with a reversibility test and PEF/FEV1 monitoring with AsthmaTuner during 2-4 weeks, and secondly randomization to traditional trial treatment with dynamic spirometry with a reversibility test, or AsthmaTuner incl. PEF/FEV1 monitoring during trial treatment. We plan to include in total 146 patients in primary care with either undiagnosed asthma having respiratory symptoms that can be signed to asthma last month, or patients with a asthma diagnosis last 5 years but no intake of regular anti-inflammatory asthma medication last 3 months. The study start in early 2021 and finish in 2023.

NCT ID: NCT04642716 Completed - Periodontitis Clinical Trials

Evaluation of Free Aminoacids in Saliva as A Diagnostic Biomarker of Periodontal Disease

Start date: April 20, 2015
Phase: N/A
Study type: Interventional

Amino acids (AAs) are organic molecules that are associated with inflammation and innate immunity diseases with critical roles in the cell repair and protection process. Our aim was to identify the free amino acids in saliva of a group of periodontitis patients and healthy individuals and additionally to assess their levels in different periodontal disease types and compare it to the healthy individuals.