Skip to content

Effect of Different Doses of Perioperative Dexmedetomidine on Postoperative Gastrointestinal Function in Laparoscopic Colorectal Cancer Patients: A Randomized Controlled Clinical Trial

Effect of Different Doses of Perioperative Dexmedetomidine on Postoperative Gastrointestinal Function in Laparoscopic Colorectal Cancer Patients: A Randomized Controlled Clinical Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500097778
Enrollment
Unknown
Registered
2025-02-25
Start date
2024-09-02
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

Colorectal cancer

Interventions

Group C:Before operation, dexmedetomidine was continuously infused at 0.5ug/kg in group D1 and group D2, and the infusion ended within 15 min before induction, and the same amount of normal saline was
Group D1:Before operation, dexmedetomidine was continuously infused at 0.5ug/kg in group D1 and group D2, and the infusion ended within 15 min before induction, and the same amount of normal saline wa
Group D2:Before operation, dexmedetomidine was continuously infused at 0.5ug/kg in group D1 and group D2, and the infusion ended within 15 min before induction, and the same amount of normal saline wa

Sponsors

The Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age>=18 years 2. ASA classification I.-III 3. BMI between 18-25 4. Consent to surgery and sign informed consent

Exclusion criteria

Exclusion criteria: 1. Allergy to dexmedetomidine or other anesthetic drugs 2. Alcoholism or neuropsychiatric diseases 3. Long-term use of sleeping pills and sedatives 4. Opioid abuse 5. Bradyarrhythmia with baseline heart rate 800 mL) 10. Emergency reoperation

Design outcomes

Primary

MeasureTime frame
Time to first postoperative flatgas;

Secondary

MeasureTime frame
Postoperative I-FEED quality score;Time to first bowel movement;Time to first oral eating;Postoperative pain quality score;Postoperative nausea and vomiting score;Postoperative Qor-15 score;Postoperative sleep quality (AIS) score;

Countries

China

Contacts

Public ContactQi Dunyi

The Affiliated Hospital of Xuzhou Medical University

1732509578@qq.com+86 151 6215 9886

Outcome results

None listed

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