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Evaluation of the Efficacy of Self-made Magnetically Controlled Capsule Endoscopy Sugar Coating Traction Aids Combined with Traditional Chinese Sugar Painting Technology in Observing the Efficacy of the Cardia

Evaluation of the Efficacy of Self-made Magnetically Controlled Capsule Endoscopy Sugar Coating Traction Aids Combined with Traditional Chinese Sugar Painting Technology in Observing the Efficacy of the Cardia

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400079874
Enrollment
Unknown
Registered
2024-01-15
Start date
2023-06-25
Completion date
Unknown
Last updated
2024-01-22

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

Conditions

Diseases of the cardia

Interventions

Group A:Swallowing without any drawstring MCE using traditional methods
Group B:Completion of suction cup lanyard-assisted MCE using a single-use capsule endoscopic detachable retractor wire
Group C:Adoption of the sugar-coated tethered MCE system

Sponsors

Binzhou Medical University/ Binzhou Medical University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 99 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: individuals who (1) met the parameters of the Chinese Guidelines for Clinical Application of Magnetic Capsule Gastroscopy (2021, Shanghai), (2) signed the informed consent and voluntarily participated in this study, and (3) had no history of diabetes mellitus were included in this investigation.

Exclusion criteria

Exclusion criteria: (1) who had common small bowel capsule endoscopy or MRI contraindications, absolute contraindications without surgical conditions or refused to undergo any abdominal surgery (including endoscopic surgery), (2) with in-vivo cardiac pacemakers, cochlear implants, drug perfusion pumps, neurostimulators, and other electronic devices and magnetic metal objects, except for the MRI-compatible products, (3) who because of the physical state or mental and psychological reasons cannot be examined, including pregnant women, and (4) with known or suspected gastrointestinal obstruction, stenosis, and fistula swallowing dysfunction were excluded from the study.

Design outcomes

Primary

MeasureTime frame
Visualisation of cardia observation;

Secondary

MeasureTime frame
lesion detection rate;Occurrence of adverse events;Inspection time;comfort;

Countries

China

Contacts

Public ContactChang Lujie

Binzhou Medical University Hospital

clj08642@163.com+86 158 9889 7814

Outcome results

None listed

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