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Effects of Remimazolam and Dexmedetomidine on Postoperative Gastrointestinal Function After Laparoscopic Colon Cancer Surgery: A Randomized Controlled Trial

The Effect of Remimazolam and Dexmedetomidine on Postoperative Gastrointestinal Function in Laparoscopic Colon Cancer Surgery: A Randomized Controlled Study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116036
Enrollment
Unknown
Registered
2026-01-05
Start date
2026-01-20
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Colon cancer

Interventions

Dexmedetomidine Group:Dexmedetomidine
Remimazolam Group:Remimazolam

Sponsors

Army Medical Center of PLA
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Patients scheduled to undergo elective laparoscopic colon cancer surgery under general anesthesia; 2.American Society of Anesthesiologists (ASA) physical status classification: I–III; 3.Age: >=18 years; 4.Body mass index (BMI): 18–30 kg/m^2; 5.Normal cognitive function; 6.Expected operative duration: 1–6 h; 7.Written informed consent provided.

Exclusion criteria

Exclusion criteria: 1.Known allergy to the investigational drugs; 2.History of severe cardiac (second- or third-degree atrioventricular block or baseline heart rate <50 beats/min), hepatic (Child–Pugh class C), or renal dysfunction (requiring renal replacement therapy); 3.Preexisting gastrointestinal dysfunction before surgery (intestinal obstruction or inflammatory bowel disease); 4.Previous history of abdominal surgery. 5.Planned or unplanned perioperative stoma creation; 6.Conversion from laparoscopic to open surgery; 7.Inability to complete extubation in the operating room, requiring transfer to the ICU with an endotracheal tube in place; 8.No use of postoperative patient-controlled analgesia (PCA).

Design outcomes

Primary

MeasureTime frame
Time to first flatus after surgery;

Secondary

MeasureTime frame
Postoperative Gastrointestinal Function (I-FEED) Score;The quality of recovery in the first three postoperative days was assessed using the QoR-15 Score.;Incidence of Perioperative Adverse Events;Intestinal Function Recovery Rate at 72 Hours Postoperatively;Time to first oral intake postoperatively;Perioperative Opioid Consumption;

Countries

China

Contacts

Public ContactQingxiang Mao

Army Medical Center of PLA

maomaosmmu@126.com+86 13594054231

Outcome results

None listed

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