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Search / Trial NCT05949229

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

Launched by AMIRA HASSAN AHMED ALI · Jul 10, 2023

Trial Information

Current as of July 09, 2025

Not yet recruiting

Keywords

Duloxetine, Pod, Postoperative Dilrium

ClinConnect Summary

This clinical trial is studying whether taking a medication called duloxetine before cancer surgery can help reduce the chances of patients experiencing postoperative delirium, which is a serious condition that can cause confusion and changes in mental status after surgery. The trial will involve adult patients who are preparing for surgery to treat cancer, and it aims to find out if duloxetine can make a difference.

To participate, patients need to be adults who are healthy enough for surgery and can understand the study, as they will need to provide consent. However, individuals with certain conditions, such as existing cognitive issues or severe mental health problems, will not be eligible. This trial is not yet recruiting participants, but once it begins, those who qualify will be given either duloxetine or a placebo (a harmless pill with no active medication) before their surgery. The goal is to see if taking duloxetine helps them recover better and avoids confusion afterward.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • All patients will sign an informed consent prior to inclusion in the study.
  • Adult patients with ASA class I-III, undergoing cancer surgery.
  • Exclusion Criteria:
  • Patients with pre-existing neuro- cognitive dysfunction.
  • Documented signs of dementia after psychiatric evaluations.
  • Language barriers or deafness.
  • Psychosis stroke, meningitis, or brain tumors

About Amira Hassan Ahmed Ali

Amira Hassan Ahmed Ali is a dedicated clinical trial sponsor committed to advancing medical research and improving patient outcomes through innovative clinical studies. With a strong focus on ethical standards and regulatory compliance, Amira oversees the design, implementation, and management of clinical trials across various therapeutic areas. Her expertise in project management and collaboration with multidisciplinary teams ensures the successful execution of trials, fostering an environment of scientific rigor and integrity. Through her leadership, Amira aims to contribute significantly to the development of new treatments and therapies that enhance the quality of care for patients worldwide.

Locations

Assiut, , Egypt

Patients applied

0 patients applied

Trial Officials

Amira Hassan Ahmed, resident

Principal Investigator

Faculty of medecine,assiut,Egypt

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported