Capsule Endoscopy
Conditions
Keywords
Magnetically controlled capsule endoscopy, sucralfate gel, drug behavior, upper-gastrointestinal tract
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).
Interventions
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.
Sponsors
Changhai Hospital
Study design
Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes
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
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Sucralfate gel adhesion behavior in the fasted gastric cavity | 180 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 cavity | 0, 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 cavity | 180 minutes | The dissipation time was evaluated by calculating the times between sucralfate gel entered the stomach and adhered sucralfate disappeared completely. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Number of Participants with complications of MCE | 2 weeks | Any complications associated with MCE. |
| Discomfort scores of participants during the procedure | during 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). |
Countries
China
Outcome results
None listed