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Not Yet RecruitingNCT07097038

Analgesic Effect and Safety of Oliceridine and Oxycodone in Vitrectomy

Analgesic Effect and Safety of Oliceridine and Oxycodone in Vitrectomy: a Randomized Controlled Trial

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
120 (estimated)
Sponsor
Henan Provincial People's Hospital · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Accepted

Summary

Traditional opioid analgesia is a method to treat moderate to severe pain. However, the use of opioids is not without risks. When treating acute pain, patients may have hypotension, respiratory depression, hypoxia, nausea and vomiting, irritability and pruritus. The aim of this study was to evaluate the analgesic effect and safety of g-protein-biased μ - opioid receptor agonists Oliceridine and oxycodone in vitrectomy.

Detailed description

a total of 120 patients scheduled for vitrectomy were randomly divided into Oliceridine group (n = 60) and oxycodone group (n = 60). The main outcome measure was visual analogue scale (VAS) at 2 hours after operation, and the secondary outcome measures included intraoperative analgesic drug addition, VAS scores at 6 and 24 hours after operation, respiratory depression (oxygen saturation \< 90%) and incidence of adverse reactions (nausea, vomiting, dizziness).

Conditions

Interventions

TypeNameDescription
DRUGOliceridineIntraoperative analgesia should be administered with Oliceridine
DRUGOxycodoneOxycodone is used for intraoperative analgesia

Timeline

Start date
2025-07-01
Primary completion
2025-12-01
Completion
2026-07-01
First posted
2025-07-31
Last updated
2025-07-31

Source: ClinicalTrials.gov record NCT07097038. Inclusion in this directory is not an endorsement.