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
| Type | Name | Description |
|---|---|---|
| DRUG | Vortioxetine 20Mg Tab | 20 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.