|drug1003||Ddrops® products, 50,000 IU, Oral Wiki||1.00|
|drug3633||Vitamin D3 Wiki||0.41|
|D004066||Digestive System Diseases NIH||0.58|
|D005767||Gastrointestinal Diseases NIH||0.58|
|D003141||Communicable Diseases NIH||0.07|
There is one clinical trial.
In December 2019, an outbreak of pneumonia associated with a novel coronavirus named as severe acute respiratory syndrome coronavirus 2 (SARSCoV-2) was reported in Wuhan city, China, and spread exponentially throughout China and other countries in the following weeks. It is recommended that elective endoscopies should be deferred during the COVID-19 outbreak for the potential transmission between patients and medical staff in the statements of Asian Pacific Society for Digestive Endoscopy (APSDE-COVID statements). Therefore, exploring an alternative for patients with the requirements of endoscopy during the outbreak is of great importance. Herein,the investigators developed an novel non-contact magnetically-controlled capsule endoscopy (Nc-MCE) system (Figure 1) adds a remote control workstation and a audio-visual exchange system to the original well-established MCE system. This study was a open-label, prospective, randomized controlled study approved by the institutional review board of Shanghai Changhai Hospital. It was designed to evaluate the diagnostic utility, safety, feasibility and patients acceptability of Nc-MCE in patients with an indication of endoscopy, and comparing it with the result of MCE.
Description: Maneuverability score was the sum of four subjective scores rated by the operator (signal transmission quality score, operating comfort score, gastric visualization score and study subject compliance score), each of which ranged from 1 to 5 denoting the lowest to the highest degree of satisfaction.Measure: Maneuverability score Time: During the procedure
Description: GET was defined as the time time taken for the endoscopist to complete the gastric examination to his or her satisfactionMeasure: Gastric examination time(GET) Time: During the procedure
Description: The investigators use a satisfaction questionnaire to evaluate the comfort and acceptability of each patientMeasure: the comfort and acceptability of patients Time: After the procedure(within 5 days)
Description: Diagnosis based on the data of nc- MCE by two endoscopistMeasure: diagnostic yield Time: after the procedure(within 5 days)
Description: Adverse events during and after the procedureMeasure: Adverse events Time: During and within 2 weeks after the procedure
Description: Complete observation of the mucosa (>90% of the mucosa observed) in gastric cardia, fundus, body, angulus, antrum and pylorusMeasure: Clinical success Time: During the procedure
Data processed on January 01, 2021.
An HTML report was created for each of the unique drugs, MeSH, and HPO terms associated with COVID-19 clinical trials. Each report contains a list of either the drug, the MeSH terms, or the HPO terms. All of the terms in a category are displayed on the left-hand side of the report to enable easy navigation, and the reports contain a list of correlated drugs, MeSH, and HPO terms. Further, all reports contain the details of the clinical trials in which the term is referenced. Every clinical trial report shows the mapped HPO and MeSH terms, which are also hyperlinked. Related HPO terms, with their associated genes, protein mutations, and SNPs are also referenced in the report.Drug Reports MeSH Reports HPO Reports