Pronase Granules in Gastric Cleaning
Gastric Disease, Capsule Endoscopy
About this trial
This is an interventional diagnostic trial for Gastric Disease focused on measuring capsule endoscopy, pronase granules, gastric preparation, visualization of gastric mucosa, randomized controlled study
Eligibility Criteria
Inclusion Criteria:
- Age ≥ 18 years old.
- Those who underwent upper gastrointestinal and small intestinal mucosal examination under magnetically controlled capsule endoscopy at Shanghai Changhai Hospital and Chinese People's Liberation Army General Hospital after January 2020.
- Able to provide informed consent.
Exclusion Criteria:
- dysphagia or symptoms of gastric outlet obstruction, suspected or known intestinal stenosis, overt gastrointestinal bleeding, history of upper gastrointestinal surgery or abdominal surgery altering gastrointestinal anatomy, or post-abdominal radiation;
- congestive heart failure, renal insufficiency, use of anticoagulant medication,
- implanted metallic devices such as pacemakers, defibrillators, artificial heart valves or joint prostheses (although the low magnetic field used technically should not interfere with such devices);
- pregnancy;
- currently participating in another clinical study.
- Patients who fail to follow the prescribed procedures for magnetically controlled capsule endoscopy;
- Patients who only undergo gastric examination under magnetically controlled capsule endoscopy;
- Patients who only undergo small bowel examination under magnetic control capsule endoscopy;
- The patient's basic information in the database is incomplete#
- Patient fail to be followed up.
Sites / Locations
- Changhai HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Placebo Comparator
Experimental
Control group
Pronase group
All patients underwent a bowel preparation that consisted of a low-residue diet for 24 hours, fluid intake, and ingestion of two liters of polyethylene glycol-based electrolyte solution 12 hours before the examination. On the examination day, patients arrived at the hospital in the morning after an overnight fast (>8hours). Then they would be randomly assigned to the control group or pronase group randomly. 40 minutes before capsule ingestion, all patients swallowed 100ml clear water containing 50mg dimethicone. And 25 minutes before swallowing the capsule, the patient was asked to take 200ml warm water. There is still have 800-1000ml water for gastric filling 10 minutes before swallowing the capsule.
All patients underwent a bowel preparation that consisted of a low-residue diet for 24 hours, fluid intake, and ingestion of two liters of polyethylene glycol-based electrolyte solution 12 hours before the examination. On the examination day, patients arrived at the hospital in the morning after an overnight fast (>8hours). Then they would be randomly assigned to the control group or pronase group randomly. 40 minutes before capsule ingestion, all patients swallowed 100ml clear water containing 50mg dimethicone. And 25 minutes before swallowing the capsule, the patient was asked to take 20000 IU pronase Granules Combined with 1 g NaHCO3 dissolved in 200ml warm water to maintain the intragastric pH at 6 - 8. There is still have 800-1000ml water for gastric filling 10 minutes before swallowing the capsule.