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Comfort Application of Oxycodone in Perioperative Analgesia

Comfort Application of Oxycodone in Perioperative Analgesia

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083623
Enrollment
Unknown
Registered
2024-04-29
Start date
2022-06-28
Completion date
Unknown
Last updated
2024-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative visceral pain

Interventions

Group N1:Hydroxycodone was given
Group N2:Sulfentanil was given

Sponsors

Wuxi People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients = 18 years of age, ASA grade I to III, intended for abdominal surgery and digestive endoscopy under general anesthesia

Exclusion criteria

Exclusion criteria: Emergency surgery, body mass index = 35 kg/m2, allergy to the drugs in the study, severe cardiopulmonary disease, severe cerebrovascular disease, severe liver and kidney disease (Child-Pugh grade C, renal replacement therapy), severe neurological disease, preoperative cognitive impairment (MMSE score =)23 points), use of antipsychotics, alcohol abuse, long-term opioid or other analgesic drugs, inability to understand the postoperative recovery scale, inability to understand the pain rating scale, failure to provide informed consent

Design outcomes

Primary

MeasureTime frame
Visceral pain at overall rest within 24 hours after surgery;

Secondary

MeasureTime frame
Visceral pain during the overall cough within 24 hours after surgery;Consumption of analgesic and postoperative drugs;Nausea and vomiting;

Countries

China

Contacts

Public ContactQian Yiling

Wuxi People's Hospital

ylqian_1987@163.com+86 189 1526 5254

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026