Clinical Trials Directory

Trials / Completed

CompletedNCT06561438

Postoperative Pain Management Following Laparoscopic Cholecystectomy

Postoperative Pain Management Following Laparoscopic Cholecystectomy- Vortioxetine

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
86 (actual)
Sponsor
Future University in Egypt · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

Postoperative pain management is essential and the inability to treat acute pain appropriately in the first 48 postoperative hours represents a risk factor for developing chronic pain. No. study has investigated Vortioxetine as an adjuvant to standard care for postoperative pain management in patients undergoing LC

Detailed description

Postoperative pain is a main challenge for delayed hospital discharge in Laparoscopic cholecystectomy. . Postoperative pain management is essential and the inability to treat acute pain appropriately in the first 48 postoperative hours represents a risk factor for developing chronic pain. Vortioxetine (VO) is a multimodal serotonergic antidepressant with a unique mechanism of action that is effective in treating neuropathic pain. The purpose of this study is evaluating the efficacy and tolerability of preoperative oral administration of Vortioxetine on postoperative pain control in patients undergoing LC

Conditions

Interventions

TypeNameDescription
DRUGVortioxetine 20Mg Tab20 mg oral vortioxetine tablet 2 hours before the procedure

Timeline

Start date
2024-08-06
Primary completion
2025-06-07
Completion
2025-06-07
First posted
2024-08-20
Last updated
2025-06-22

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT06561438. Inclusion in this directory is not an endorsement.