The effect of different analgesics on pain events in postoperative ventilated patients: a multicenter trial

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100051176

Enrollment

Unknown

Registered

2021-09-15

Start date

2021-09-20

Completion date

Unknown

Last updated

2022-05-23

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

Conditions

Critically ill ventilated patients

Interventions

Experimental group:Oxycodone

Control group:NSAIDs

Eligibility

Sex/Gender

All

Age

18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Postoperative ventilated patients longer than 24 hours.

Exclusion criteria

Exclusion criteria: Patients are reluctant to attend the trial.

Design outcomes

Primary

Measure	Time frame
behavior pain score;	—

Secondary

Measure	Time frame
dosage of sedatives;duration of mechanical ventilation;	—

Countries

China

Contacts

Public ContactXing Xuezhong

Department of Intensive Care Unit, /Cancer Hospital, Chinese Academy of Medical Sciences

xingxuezhong@cicams.ac.cn+86 10 18601141 437

Outcome results

None listed

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