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Study of no-background oxycodone PCIA in post-operative pain management

Study of no-background oxycodone PCIA in post-operative pain management

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800015183
Enrollment
Unknown
Registered
2018-03-12
Start date
2017-11-01
Completion date
Unknown
Last updated
2018-03-19

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

Conditions

Post-Operative Pain

Interventions

No background Group:no background oxycodone infusion
Background Group:background oxycodone infusion

Sponsors

Sun Yat-sen University Cancer Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients between the ages of 18 and 65 years with ASA classification of I or II; 2. Scheduled for laparoscopic radical resection of colorectal cancer under incubated general anesthesia; 3. Adequate informed consent.

Exclusion criteria

Exclusion criteria: 1. Long term users of steroids, opioids or psychotropic medication; 2. Patients taking MAO inhibitor in two weeks before surgery; 3. Patients who are alcoholics; 4. ASA classification III or more, severe systemic condition

Design outcomes

Primary

MeasureTime frame
Oxycodone consumption;Post-operative pain;—

Secondary

MeasureTime frame
Satisfaction score;—

Countries

China

Contacts

Public ContactHUANG Wan

Sun Yat-sen University Cancer Center

huangwan@sysucc.org.cn+86 13924103792

Outcome results

None listed

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