Skip to content

Comparison of Sodium Picosulfate/Magnesium Citrate Solution with Polyethylene Glycol Electrolyte Solution for Preoperative Bowel Preparation in Colonoscopy: A Single-Center, Randomized, Controlled Clinical Study

Comparison of Sodium Picosulfate/Magnesium Citrate Solution with Polyethylene Glycol Electrolyte Solution for Preoperative Bowel Preparation in Colonoscopy: A Single-Center, Randomized, Controlled Clinical Study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081004
Enrollment
Unknown
Registered
2024-02-20
Start date
2023-10-27
Completion date
Unknown
Last updated
2024-02-26

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

Conditions

colon

Interventions

Test group:The first dose should be taken from 18:00 to 20:00 the night before the colonoscopy. The specific method is as follows: (1) Pour a bottle of magnesium sulfate sodium potassium oral concent
Control group :1, the night before the examination, two hours after dinner, take 2 boxes of Sutaiqing, each box of Sutaiqing with 750ml plain water, taken within 1 hour. 2, On the day of the examinat

Sponsors

Department of Digestive Oncology, Civil Aviation General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1: Patients between 18 and 70 years old who are planned to receive treatment under colonoscopy, regardless of gender 2: Willing to sign a written informed consent, including agreeing to participate in the screening procedures to determine eligibility 3: Able to communicate effectively with the researcher and comply with the protocol requirements 4: take the bowel-cleansing medication correctly according to the study requirements

Exclusion criteria

Exclusion criteria: 1: A history of acute myocardial infarction (within 6 months), severe cardiovascular, hepatic or renal dysfunction, or mental disorders. 2: Taking anticoagulant drugs such as aspirin or warfarin, or having coagulation dysfunction 3: Patients taking or previously taking liraglutide, or known to have an allergy to liraglutide 4: Participants who are pregnant or planning to become pregnant during the study period 5: Patients with inflammatory bowel disease, chronic diarrhea, severe gastroparesis or intestinal obstruction 6: Currently participating in other clinical observation trials or participated in other clinical trials within 60 days

Design outcomes

Primary

MeasureTime frame
The Boston Bowel;

Secondary

MeasureTime frame
Evaluation of intestinal bubble under colonoscopy;Defecation frequency;Cecal intubation rate;Ready-Interval between colorectal exams;time of operation ;Detection rate of adenoma and polyp;Sleep quality;Patient tolerance;Incidence of drug-related complications;Surgery-related incidence;

Countries

China

Contacts

Public ContactJianping Cheng

Civil Aviation General Hospital

cjpczy2004@163.com+86 158 1128 2039

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 5, 2026