Track this trial free. DataLookout checks ClinicalTrials.gov daily and emails you which fields changed on NCT07018375 (status, enrollment, completion dates, endpoints, sites) when this record is updated. Free accounts track up to 5 trials.

Track this trial

Effect of Oliceridine Patient-Controlled Intravenous Analgesia on Postoperative Chronic Pain After Video-Assisted Thoracoscopic Lung Resection

StatusRecruiting
PhasePhase 4
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary endpoint reworded 1 of 1 changed
See other at-risk trials from Tianjin Medical University General Hospital

Record History

See every version on ClinicalTrials.gov ↗

  1. Primary endpoint(s) modifiedv5 Show 4 more changesShow less
    • Trial status changed: Enrolling by Invitation → Recruiting
    • Trial sites expanded: 1 → 7 locations
    • Eligibility criteria expanded, about 22 words
    • Secondary endpoints: details revised at 5 of 11 entries
  2. Primary endpoint revisedv4 Show 7 more changesShow less
    • Trial status: Enrolling by Invitation to Recruiting
    • Study sites: 1 to 7
    • Eligibility criteria expanded, about 13 words
    • Secondary endpoints: 9 to 11
    • Study description expanded, about 21 words
    • Collaborators expanded, about 38 words
    • Study title revised
  3. Trial status changed: Not Yet Recruiting → Enrolling by Invitation
    • Study sites: 0 to 1
    v3
  4. Start date: Aug 1, 2025 to Jan 6, 2026v2
  5. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The primary objective is to evaluate the impact of oliceridine versus sufentanil for perioperative analgesia on the incidence of chronic postsurgical pain (CPSP) with functional impact in patients undergoing video-assisted thoracoscopic surgery.
Trial Details
NCT Number NCT07018375
Lead Sponsor Tianjin Medical University General Hospital
Collaborators: The No. 2 Hospital of Baoding, Tianjin Cancer Hospital Airport Hospital, Tianjin Medical University Second Hospital, North China University of Science and Technology, Haibin People's Hospital of Tianjin Binhai New Area, The People's Hospital of Jizhou District, Tianjin
Conditions
(from sponsor)		 Chronic Postsurgical Pain
Related terms Postoperative Pain
Enrollment 320 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov