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MCE Direct Visualization of Drug Behavior in Upper-gastrointestinal Tract

Completed
Conditions
Capsule Endoscopy
Interventions
Device: Magnetically controlled capsule endoscopy
Registration Number
NCT04327869
Lead Sponsor
Changhai Hospital
Brief Summary

The investigators aim to explore the feasibility of MCE in direct, real-time visualization of drug behavior in upper-gastrointestinal tract, which presented by the adhesion, distribution, and dissipation characteristics of dyed sucralfate gel.

Detailed Description

This pilot study was a prospective, single-centered, nonrandomized study. The investigators selected 10 subjects from patients with a recent history of upper-gastrointestinal symptoms who met the indication of taking sucralfate suspension gel, and another 10 subjects from healthy volunteers.

Procedures were performed by the NaviCam magnetic capsule guidance system. To enhance discrimination, the sucralfate gel dyed with 0.3 ml methylene blue. The subjects swallowed the capsule with water in the left lateral position. When capsule enter stomach cavity, subject was asked to sit up and ingested 4 g aerogenic powder with 5 ml water to distend the stomach, and performed gastric baseline examinations to identify the lesions. After baseline examination, subjects ingested dyed sucralfate gel and performed the first-time examination. The examination was repeated at 30 min intervals, until dyed sucralfate gel disappeared completely. When study completed, the capsule was detached from string and continued into the small bowel for further examination.

The endoscopists recorded the adhesion and dissipation times of dyed sucralfate gel, calculated the efficient time, and selected the images of six primary anatomic landmarks from each examination to measure the distribution area (%) . Any complication or discomfort during the procedure was evaluated. The discomfort was scored on a scale from 0 to 3 (0 = no; 1 = mild/minimal; 2 = moderate; 3 = sever/very difficult).

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
20
Inclusion Criteria
  • With or without gastrointestinal complaints
  • Scheduled to undergo a capsule endoscopy for both stomach and small bowel
  • Signed the informed consents before joining this study
Exclusion Criteria
  • Suspected or known gastrointestinal stenosis
  • Obstruction or other known risk factors for capsule retention
  • Pregnancy or suspected pregnancy
  • Pacemakers or electromedical devices implanted
  • Any other contraindications determined by endoscopists

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Healthy control groupMagnetically controlled capsule endoscopyThe investigators selected another 10 subjects (male: female = 1: 1) from healthy volunteers.
Abdominal symptoms groupMagnetically controlled capsule endoscopyThe investigators selected 10 subjects (male: female = 1: 1) from patients with a recent history of upper-gastrointestinal symptoms who met the indication of taking sucralfate suspension gel
Primary Outcome Measures
NameTimeMethod
Sucralfate gel adhesion behavior in the fasted gastric cavity180 minutes

The adhesion time was recorded from the sucralfate gel entered the stomach to all sucralfate adhered to the gastric wall.

Sucralfate gel distribution behavior in the fasted gastric cavity0, 30, 60, 90, 150, 180 min after dyed sucralfate gel enter the stomach

The distribution area of sucralfate gel was measured by selecting images of six primary anatomic landmarks (cardia, fundus, body, angulus, antrum, and pylorus) at different times, the images were imported into MATLAB software to calculate the area of sucrafate gel. The dynamic changes of distribution area of sucralfate gel over the time were analyzed and performed with GraphPad Prism.

Sucralfate gel dissipation behavior in the fasted gastric cavity180 minutes

The dissipation time was evaluated by calculating the times between sucralfate gel entered the stomach and adhered sucralfate disappeared completely.

Secondary Outcome Measures
NameTimeMethod
Number of Participants with complications of MCE2 weeks

Any complications associated with MCE.

Discomfort scores of participants during the procedureduring the procedure

The discomfort associated with the procedure included swallow difficulty, nausea caused by string, pulling capsule up and down, abdominal distension or pain caused by ingesting aerogenic powder, discomfort during MCE examination, and pulling the string out. The discomfort was scored on a scale from 0 to 3 (0 = no; 1 = mild/minimal; 2 = moderate; 3 = sever/very difficult).

Trial Locations

Locations (1)

Changhai Hospital

🇨🇳

Shanghai, China

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