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Correlation between time interval after gastric emptying with ultrasound assessment and quality of bowel cleansing in patients undergoing painless colonoscopy: a randomized, prospective,controlled trial

Correlation between time interval after gastric emptying with ultrasound assessment and quality of bowel cleansing in patients undergoing painless colonoscopy: a randomized, prospective,controlled trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072784
Enrollment
Unknown
Registered
2023-06-25
Start date
2023-07-01
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

Painless gastroenteroscopy

Interventions

Group A: 2-4h after taking polyethylene glycol on the day of colonoscopy (Group A):Colonoscopy was completed 2 to 4 hours after completion of polyethylene glycol administration
Group B: 4-6h after taking polyethylene glycol on the day of colonoscopy (Group B):Colonoscopy was completed 4 to 6 hours after completion of polyethylene glycol administration

Sponsors

Nanjing First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: A total of 100 patients were selected for colonoscopy or intestinal polypectomy under non-intubation general anesthesia. They were of all genders, aged 18-70 years, BMI 18-25 kg/m^2, ASA grade I or II

Exclusion criteria

Exclusion criteria: Patients with serious heart and lung diseases who cannot tolerate anesthesia or gastroenteroscopy; Patients with chronic constipation, poor bowel preparation as required (e.g., preoperative high-fiber diet, inadequate PEG dosage), history of gastric or intestinal surgery, history of other medical conditions (e.g., diabetes, Parkinson's disease, stroke, or spinal cord injury), use of tricyclic antidepressants or anesthetics and other risk factors for inadequate bowel preparation; Patients who had participated in or were participating in other clinical trials within 3 months prior to enrollment.

Design outcomes

Primary

MeasureTime frame
Intestinal cleansing quality and satiety rate at different waiting times after taking intestinal cleansing solution;

Secondary

MeasureTime frame
Gastric emptying time;Colonoscopy operation time;Rate of ileal intubation;The detection rate of polyp and adenoma;Patient satisfaction;

Countries

China

Contacts

Public ContactTao Shan

Nanjing First Hospital

shantao2021@163.com+86 188 5209 5135

Outcome results

None listed

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