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Evaluation and Application of Three Observational Pain Assessment Scales on Postoperative Pain Assessment during Recovery Period in Adults with Abdominal Surgery

Evaluation and Application of Three Observational Pain Assessment Scales on Postoperative Pain Assessment during Recovery Period in Adults with Abdominal Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400093591
Enrollment
Unknown
Registered
2024-12-09
Start date
2025-01-01
Completion date
Unknown
Last updated
2024-12-16

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

Conditions

Assess postoperative acute pain

Interventions

Abdominal patients who enter the anesthesia recovery room after surgery 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.Age >= 18 years old; 2.Preoperative cognitive function was normal; 3.The anesthesia method adopts general anesthesia; 4.No significant physical or mental complications before surgery; 5.American Society of Anesthesiologists (ASA) classification <= III; 6.When entering PACU, self-reported pain cannot be measured using a language scale, and the Richmond Agitation Sedation Scale (RASS) ranges from -4 to -2; 7.The patient was successfully sent back to the ward after recovery; 8.Voluntarily signed informed consent.

Exclusion criteria

Exclusion criteria: 1.Patients with impaired preoperative cognitive function who are unable to complete preoperative visits normally; 2.Emergency surgery patients who do not receive general anesthesia; 3.Preoperative severe physical or mental diseases such as diabetes, cardiopulmonary insufficiency, mental disorders, etc; 4.Preoperative use of opioid therapy; 5.Patients who did not enter the recovery room after surgery or were sent to the ICU after recovery; 6.Unwilling to participate or withdraw from this study midway.

Design outcomes

Primary

MeasureTime frame
Rating of 3 scales;

Secondary

MeasureTime frame
Painful conditions;

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