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Postoperative acute pain investigation

Postoperative acute pain investigation

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900025237
Enrollment
Unknown
Registered
2019-08-17
Start date
2019-08-20
Completion date
Unknown
Last updated
2021-08-30

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

Conditions

Postoperative acute pain

Interventions

Case series:no

Sponsors

Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients who returned to the ward for more than 6 hours on the first day after operation; 2. Adult patients over or equal to 18 years old.

Exclusion criteria

Exclusion criteria: Patients do not agree to participate in the study or the patient's consciousness, cognitive state can not make a judgment as to whether to participate in this study.

Design outcomes

Primary

MeasureTime frame
VAS score;—

Secondary

MeasureTime frame
Degree of pain complications, such as Nausea, drowsiness, itching, dizziness.;patients Satisfaction;—

Countries

China

Contacts

Public ContactWeidong Mi

Chinese PLA General Hospital

chunxia.zhang@unimedsci.com+86 010-66938051

Outcome results

None listed

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