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The Impact of Different Doses of Dexmedetomidine on Postoperative Gastrointestinal Function Recovery in Patients Undergoing Gynecological Laparoscopic Surgery

The Impact of Different Doses of Dexmedetomidine on Postoperative Gastrointestinal Function Recovery in Patients Undergoing Gynecological Laparoscopic Surgery

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500099082
Enrollment
Unknown
Registered
2025-03-18
Start date
2024-04-04
Completion date
Unknown
Last updated
2025-03-24

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

Conditions

postoperative gastrointestinal dysfunction

Interventions

D0:Control Group (D0): Patients will receive an infusion of normal saline throughout the surgery.
D1:Patients will receive an initial bolus dose of 0.5 µg/kg of dexmedetomidine over 10 minutes, followed by a continuous infusion of 0.2 µg/kg/h for the remainder of the surgery.
D2:Patients will receive an initial bolus dose of 0.5 µg/kg of dexmedetomidine over 10 minutes, followed by a continuous infusion of 0.4 µg/kg/h for the remainder of the surgery.
D3:Patients will receive an initial bolus dose of 0.5 µg/kg of dexmedetomidine over 10 minutes, followed by a continuous infusion of 0.6 µg/kg/h for the remainder of the surgery.

Sponsors

Zhongda Hospital, School of Medicine, Southeast University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria 1 American Society of Anesthesiologists (ASA) Physical Status Classification I-III. 2 Patients scheduled for gynecological laparoscopic surgery. 3 Patients or their legally authorized representatives agree to sign the informed consent form. 4 Patients aged between 18 and 75 years.

Exclusion criteria

Exclusion criteria: Exclusion Criteria 1 Known gastrointestinal motility disorders. 2 History of abdominal surgery. 3 Second-degree or higher heart block. 4 Preoperative baseline heart rate below 50 beats per minute (bpm). 5 Severe hepatic or renal dysfunction. 6 Difficult airway or history of delayed extubation. 7 Opioid abuse. 8 Allergy to dexmedetomidine or other anesthetics. 9 Expected postoperative transfer to the Intensive Care Unit (ICU). 10 Pregnant women.

Design outcomes

Primary

MeasureTime frame
Time to First Flatus;

Secondary

MeasureTime frame
First defecation time;I-FEED Score;Postoperative recovery quality;Pain score;Sleep score;Nausea and vomiting score;Perioperative vital signs;First eating time;

Countries

China

Contacts

Public ContactMi Tian

Department of Anesthesiology, surgery and pain management, Zhongda Hospital, School of Medicine, Southeast University

candytianmi@126.com+86 139 1304 9496

Outcome results

None listed

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