Trials / Completed
CompletedNCT05813847
Herniorrhaphy for Postoperative Pain
A Randomized, Double-Blind, Placebo- and Active-Controlled Study to Evaluate the Efficacy and Safety of CPL-01 in the Management of Postoperative Pain After Open Inguinal Herniorrhaphy
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 518 (actual)
- Sponsor
- Cali Pharmaceuticals LLC · Industry
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
Subjects receive either CPL-01, positive control, or negative control after herniorrhaphy and are then followed.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | local anaesthetic injection | Local infiltration of study drug |
Timeline
- Start date
- 2023-04-18
- Primary completion
- 2025-09-15
- Completion
- 2025-10-06
- First posted
- 2023-04-14
- Last updated
- 2026-04-08
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT05813847. Inclusion in this directory is not an endorsement.