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Evaluation and application of three observational pain assessment scales in pain assessment during the recovery period of adult surgical anesthesia

Evaluation and application of three observational pain assessment scales in pain assessment during the recovery period of adult surgical anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500099903
Enrollment
Unknown
Registered
2025-03-31
Start date
2025-04-05
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Pain during the recovery period of general anesthesia in patients

Interventions

Observation group:None

Sponsors

Zhongshan People’s Hospital(Affiliated Zhongshan Hospital of Sun Yat-sen University)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Voluntarily sign the informed consent form; 2. Age>=18 years; 3. Normal preoperative cognitive function; 4. Anesthesia: general anesthesia; 5. No major physical and mental comorbidities before surgery; 6. American Society of Anesthesiologists (ASA) classification<=III.; 7. Unable to self-report pain using a language scale upon admission to the PACU, Richmond agitation-sedation scale (RASS) =-4 ~ -2; 8. Patients who are successfully sent back to the ward after resuscitation;

Exclusion criteria

Exclusion criteria: 1. Patients undergoing emergency surgery, patients who do not use general anesthesia; 2. Patients with impaired preoperative cognitive function and unable to complete the preoperative visit normally; 3. Preoperative concomitant major physical or psychiatric diseases such as diabetes, cardiopulmonary insufficiency, mental abnormalities, etc.; 4. Preoperative opioid therapy; Patients who are not in the resuscitation room after surgery or who are sent to the ICU after resuscitation; 5. Those who are unwilling to participate or withdraw from this study halfway.

Design outcomes

Primary

MeasureTime frame
Acute Pain Assessment Tool, APA5 ;Critical-Care Pain Observation Tool, CPOT ;the Revised Adult Nonverbal Pain Scale, NVPS-R;

Countries

China

Contacts

Public ContactHu Jiajia

Zhongshan People’s Hospital(Affiliated Zhongshan Hospital of Sun Yat-sen University)

471776757@qq.com+86 13450923162

Outcome results

None listed

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