Trials / Not Yet Recruiting
Not Yet RecruitingNCT07018375
The Effect of Oliceridine Patient-Controlled Intravenous Analgesia on Postoperative Chronic Pain After Video-Assisted Thoracoscopic Lobectomy
- Status
- Not Yet Recruiting
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 320 (estimated)
- Sponsor
- Tianjin Medical University General Hospital · Academic / Other
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
The primary objective is to evaluate the impact of oliceridine versus sufentanil for perioperative analgesia on the incidence of chronic postsurgical pain (CPSP) in patients undergoing video-assisted thoracoscopic surgery.
Detailed description
The primary objective is to evaluate the impact of oliceridine administered via patient controlled analgesia device（PCA）versus sufentanil administered via PCA on the incidence of chronic postsurgical pain (CPSP) in patients undergoing video-assisted thoracoscopic surgery.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Oliceridine | postoperative patient-controlled analgesia (PCA) |
| DRUG | Sufentanil | Sufentanil |
Timeline
- Start date
- 2026-01-06
- Primary completion
- 2027-03-31
- Completion
- 2027-04-30
- First posted
- 2025-06-12
- Last updated
- 2026-01-06
Source: ClinicalTrials.gov record NCT07018375. Inclusion in this directory is not an endorsement.