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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04032353
Other study ID # 2019SDU-QILU-150
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date December 31, 2018
Est. completion date March 1, 2020

Study information

Verified date July 2019
Source Shandong University
Contact Yanqing Li, PhD, MD
Phone 86-531-82169236
Email liyanqing@sdu.edu.cn
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of our study was to demonstrate the efficacy and feasibility of the medical consortium for screening upper gastrointestinal cancers with magnetically controlled capsule gastroscopy.


Description:

In this study, the investigators designed a propective cohort study to evaluate the the efficacy and feasibility of medical consortium for screening upper gastrointestinal cancers (MCSC) with magnetically controlled capsule gastroscopy (MCCG).


Recruitment information / eligibility

Status Recruiting
Enrollment 10000
Est. completion date March 1, 2020
Est. primary completion date December 31, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- asymptomatic subjects undergong magnetically controlled capsule gastroscopy for health checkup in medical consotium;

- subjects able to give informed consent

Exclusion Criteria:

- suspected or known intestinal stenosis, obstruction, or fistula;

- inoperability of refusal to accept any abdominal surgery;

- dysphagia or gastric paralysis;

- previous history of gastrointestinal disease;

- with pacemaker, implanted-cardiac defibrillator or other implanted electromedical devices;

- need for standard magnetic resonance imaging examination within seven days after swallowing the MCCG, unless the capsule is confirmed to have been excreted;

- other factors that are not suitable for inclusion evaluated by medical stuff

Study Design


Intervention

Other:
Medical Consortium
subjects received intensive follow-up by coordinators according to the predifined protocol of MCSC

Locations

Country Name City State
China Department of Gastroenterology, Qilu Hospital, Shandong University Jinan Shandong

Sponsors (1)

Lead Sponsor Collaborator
Yanqing Li

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Other adverse events safety assessment 12 months
Primary the incidence of upper gastrointestinal cancers, including gastric cancer and esophageal cancer. 12 months
Secondary tthe focal lesions of upper gastrointestinal tract 12 months
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