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The effectiveness of NaviCam magnetron capsule endoscopy in gastric lesions follow-up crowd: A multi-center, self-controlled clinical trial

The effectiveness of NaviCam magnetron capsule endoscopy in gastric lesions follow-up crowd: A multi-center, self-controlled clinical trial

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ODB-15007598
Enrollment
Unknown
Registered
2015-12-17
Start date
2015-12-17
Completion date
Unknown
Last updated
2017-04-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gastric mucosal lesions

Interventions

Group A:first magnetron capsule endoscopy then electronic gastroscopy
Group B:first electronic gastroscopy thenmagnetron capsule endoscopy

Sponsors

Southern Medical University, Nanfang Hospital, Department of Gastroenterology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. 18-70 years old, male or female; 2. has a clear stomach lesions (atrophic gastritis, gastric ulcer, gastric polyps, gastric cancer, gastric stromal tumors, etc.),have received medical treatment or therapy under endoscopy (APC, EMR, ESD, ligation, etc.), need regular follow-up, and these lesions need to have gastroscopy report; 3. the patient agreed to participate in this experiment, and voluntary signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. this follow-up required therapeutic endoscopy (clearly have the stomach, esophageal mucosal lesions within the required endoscopic treatment); 2. known or suspected gastrointestinal obstruction, strictures and fistula, or suffering from inflammatory bowel disease (such as Crohn's disease and ulcerative colitis), gastrointestinal dysfunction, patients with acute gastrointestinal during the current test; 3. no surgical conditions or refuse to accept any abdominal surgery (once the residence of the capsule will not be removed by surgery); 4. heart pacemakers or other electronic equipment by magnetic interference implant; 5. can not tolerate ordinary endoscopy, the patient required painless gastroscopy; 6. the patient who has been involved in this study; 7. swallowing disorders or pregnant women.

Design outcomes

Primary

MeasureTime frame
Past lesion detection rate;

Countries

China

Contacts

Public ContactSide Liu
liuside2011@163.com+86 15975537291

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026