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Comparison of intestinal preparation of 290ug linaloxin,simethicone, 1 bag of compound peg powder and 1 bag of compound peg powder, simethicone and 2 bags of compound peg powder, simethicone before colonoscopy

Comparison of intestinal preparation of 290ug linaloxin,simethicone, 1 bag of compound peg powder and 1 bag of compound peg powder, simethicone and 2 bags of compound peg powder, simethicone before colonoscopy

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900028102
Enrollment
Unknown
Registered
2019-12-11
Start date
2020-01-01
Completion date
Unknown
Last updated
2019-12-16

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

Conditions

bowel preparation before colonoscopy

Interventions

1:290ug linalotide +1 bag of compound electrolyte powder
2:2 bag of compound electrolyte powder
3:1 bag of compound electrolyte powder

Sponsors

Shandong Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Sign informed Consent form; (1) subjects agree with informed consent before screening, and to sign informed consent form voluntely, including accpeting screening procedure for diagonose; (2) Subject could have good communication with investigators and comply with protocol to conduct the study; 2. Patients aged 18-65 who underwent colonoscopy, regardless of gender;Correct use of intestinal cleansing drugs as required by the project; Case evaluation criteria: determine the mechanism and person, avoid selective data entry.

Exclusion criteria

Exclusion criteria: 1. previous history of acute myocardial infarction (within 6 months), with serious cardiac, hepatic and renal insufficiency or mental illness; 2. Patients who were taking aspirin, warfarin and other anticoagulant drugs, or having coagulation dysfunction; 3. Patients who were taking or/or had previously taken linalotide or were known to be allergic to linalotide, participants who were pregnant during the study period or who were planning to become pregnant; 4. Patients with inflammatory bowel disease, frequent diarrhea, severe gastroparesis and intestinal obstruction; 5. Patients who are participating in other clinical observation trials or participating in other clinical trials within 60 days.

Design outcomes

Primary

MeasureTime frame
Degree of intestinal cleansing;

Secondary

MeasureTime frame
Polyp/adenoma detection number;side effect;

Countries

China

Contacts

Public ContactHongwei Xu

Shandong Provincial Hospital

xu_hong_wei@sina.com+86 15168889328

Outcome results

None listed

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