The Effect of Preoperative Duloxetine on the Occurance of Postoperative Delirium in Patients Undergoing Cancer Surgery.

Trial statusNot yet recruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age20-80
SponsorAmira Hassan Ahmed Ali

About this trial

This is prospective double-blinded placebo-randomized controlled trial that aims to compare the effect of preoperative administration of oral duloxetine 60 mg on decreasing the incidence of postoperative delirium in cancer patients undergoing surgery.

Eligibility criteria

Qualifiers

All patients will sign an informed consent prior to inclusion in the study.

Adult patients with ASA class I-III, undergoing cancer surgery.

Disqualifiers

Patients with pre-existing neuro- cognitive dysfunction.

Documented signs of dementia after psychiatric evaluations.

Language barriers or deafness.

Psychosis stroke, meningitis, or brain tumors

Trial design

Treatments tested in this trial

  • Duloxetine 60 MG

Treatment groups

42 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Amira Hassan Ahmed Ali

Lead sponsor

Assiut University

Sponsor institution