Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07239479

DEXDES Trial: Dexmedetomidine-Desflurane Combination in Laparoscopic Colectomy

Efficacy and Safety of Dexmedetomidine Combined With Desflurane in Laparoscopic Colectomy: A Randomized Double-Blind Controlled Clinical Trial (DEXDES Trial)

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
40 (estimated)
Sponsor
Tam Anh Research Institute · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

This randomized double-blind controlled clinical trial aims to evaluate the efficacy and safety of combining Dexmedetomidine with Desflurane in patients undergoing elective laparoscopic colectomy. The study will assess whether the combination can reduce Desflurane consumption, improve intraoperative hemodynamic stability, and enhance postoperative recovery compared to Desflurane alone.

Detailed description

Dexmedetomidine, a selective alpha-2 adrenergic agonist, has sedative and analgesic properties without significant respiratory depression. Desflurane, a volatile anesthetic with low blood-gas solubility, allows rapid induction and emergence. Combining these two agents may provide anesthetic-sparing effects and promote faster postoperative recovery under ERAS protocols. This study will enroll 40 adult patients undergoing elective laparoscopic colectomy at Tam Anh General Hospital, Vietnam. Participants will be randomized into two groups: Dexmedetomidine + Desflurane versus Desflurane alone. The primary outcome is average Desflurane consumption per hour, with secondary outcomes including hemodynamic parameters, Fentanyl use, emergence quality, and incidence of postoperative nausea and vomiting.

Conditions

Interventions

TypeNameDescription
DRUGDexmedetomidine + DesfluraneDexmedetomidine bolus 1 µg/kg IV over 15 minutes before induction, followed by continuous infusion 0.5 µg/kg/h during surgery. Desflurane administered at 1 MAC with EtControl mode.
DRUGDesflurane + Normal SalineNormal saline infusion with identical timing and volume as the intervention group. Desflurane administered at 1 MAC with EtControl mode.

Timeline

Start date
2025-12-01
Primary completion
2026-12-31
Completion
2027-01-30
First posted
2025-11-20
Last updated
2025-12-30

Locations

1 site across 1 country: Vietnam

Source: ClinicalTrials.gov record NCT07239479. Inclusion in this directory is not an endorsement.