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Study on the effect of different analgesic protocols on postoperative analgesia

Study on the effect of different analgesic protocols on postoperative analgesia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500097032
Enrollment
Unknown
Registered
2025-02-11
Start date
2025-02-15
Completion date
Unknown
Last updated
2025-02-17

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

Conditions

postoperative pain

Interventions

Observed group (Postoperative use of analgesic pumps):None

Sponsors

Sichuan Academy of Medical Sciences-Sichuan Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients must meet all of the following options simultaneously: 1) American Society of Anaesthesiologists (ASA) classification of I ~ III; (2) Post-surgical patients with intravenous analgesic pumps.

Exclusion criteria

Exclusion criteria: 1) Postoperative transfer to ICU ; 2) Postoperative hospital stay <48h; 3) Symptoms associated with adverse analgesic reactions such as nausea, vomiting, dizziness, skin itching, and urinary retention immediately before surgery; 4) Serious adverse events in the perioperative period; 5) Any other conditions that the investigator believes make the patient unsuitable for participation in the study.

Design outcomes

Primary

MeasureTime frame
VAS;Patient satisfaction;

Secondary

MeasureTime frame
Incidence of adverse reactions associated with analgesic pumps;

Countries

China

Contacts

Public ContactPeng Li

Sichuan Academy of Medical Sciences-Sichuan Provincial People's Hospital

lipengmazui@qq.com+86 136 6816 9590

Outcome results

None listed

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