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Effect of different dosage and duration of simethicone on clarity of intestinal preparation in patients undergoing colonoscopy

Effect of different dosage and duration of simethicone on clarity of intestinal preparation in patients undergoing colonoscopy

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100047929
Enrollment
Unknown
Registered
2021-06-27
Start date
2021-07-10
Completion date
Unknown
Last updated
2022-03-07

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

Conditions

Digestive disease

Interventions

Group A:Immediately after taking the laxative, take simethicone 600mg (half bottle), and then take 600mg (half bottle) back to the room
Group B:Take Simethicone 1200mg immediately after taking the laxative
Group C:Take 600mg of simethicone 1 hour after taking the laxative, and then take another 600mg (half bottle) when you return to the room
Group D:Take Simethicone 1200mg (1 bottle) 1 hour after taking the laxative

Sponsors

Zhongda Hospital Affiliated to Southeast University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Adult patients aged 18-70 years, regardless of gender; 2. Patients undergoing colonoscopy; 3. Voluntarily accept the test and sign the informed consent before the inspection; 4. Patients who can cooperate and perform bowel preparation according to doctor's orders.

Exclusion criteria

Exclusion criteria: 1. Patients with a history of acute heart palpitations and infarction within 6 months; 2. Patients with severe heart, lung, brain and kidney complications; 3. Patients with intestinal obstruction; 4. Patients with a history of chronic constipation; 5. Patients who have undergone colon cancer surgery in the past; 6. Patients during pregnancy and lactation; 7. Patients who are allergic to simethicone or sorbitol and its salts; 8. Those who are participating in other clinical observation trials or have participated in other clinical trials within 60 days.

Design outcomes

Primary

MeasureTime frame
Defoaming effect score;

Secondary

MeasureTime frame
Intestinal preparation quality score;Detection rate of colonic polyps and adenomatous polyps;Incidence of abdominal distension and other adverse reactions in patients;Operation time of colonoscopy;

Countries

China

Contacts

Public ContactChen Jinxia

Zhongda Hospital Affiliated to Southeast University

happyc8jx@163.com+86 13705177921

Outcome results

None listed

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