Clinical Trials Directory

Trials / Completed

CompletedNCT06371638

Dexmedetomidine and Postoperative Cognitive Dysfunction (POCD)

Continuous Dexmedetomidine Infusion Reduces Postoperative Cognitive Dysfunction and Postoperative Pain in Patients Undergoing Laparatomy

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
112 (actual)
Sponsor
Udayana University · Academic / Other
Sex
All
Age
18 Years – 99 Years
Healthy volunteers
Not accepted

Summary

Postoperative cognitive dysfunction (POCD) affects all age groups and can lead to increased morbidity and more extended hospital stays. Dexmedetomidine reduces POCD by inhibiting the increase in proinflammatory cytokines IL-6 and TNF-α, and its anti-inflammatory activity contributes to its protective effect. Previous studies found that dexmedetomidine reduced POCD incidence in non-cardiac and cardiac surgery. Therefore, the goal of this study was to specifically investigate if using TCI dexmedetomidine to maintain anaesthesia in laparotomy surgeries reduces the incidence of POCD compared to inhalation anaesthesia by sevoflurane.

Conditions

Interventions

TypeNameDescription
DRUGDexmedetomidineGeneral anaesthesia for subjects in Group D was maintained by target-controlled infusion (TCI) dexmedetomidine (Dyck mode) with target plasma of 1 ng/ml
DRUGSevofluraneGeneral anaesthesia for subjects in Group I was maintained by inhalation anaesthesia using sevoflurane at 0.8% concentration.

Timeline

Start date
2024-01-07
Primary completion
2024-03-01
Completion
2024-03-07
First posted
2024-04-17
Last updated
2024-04-19

Locations

1 site across 1 country: Indonesia

Source: ClinicalTrials.gov record NCT06371638. Inclusion in this directory is not an endorsement.