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the Effect of Preoperative Pain Education by Anesthesia Nurses on Postoperative Pain Among Adult Patients Undergoing Abdominal Surgery

the Effect of Preoperative Pain Education by Anesthesia Nurses on Postoperative Pain Among Adult Patients Undergoing Abdominal Surgery

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06327282
Enrollment
116
Registered
2024-03-25
Start date
2024-06-15
Completion date
2025-04-04
Last updated
2024-05-23

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

Conditions

Postoperative Pain

Brief summary

To explore the effects of preoperative pain education on postoperative pain among patients undergoing abdominal surgery.

Interventions

BEHAVIORALeducation on pain and related knowledge

Before surgery, pain related knowledge was educated.

Sponsors

Chinese PLA General Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. voluntary informed consent; 2. age older than 18 years 3. abdominal surgery under elective general anesthesia

Exclusion criteria

1. Patients taking long-term analgesics (including opioids, non-steroids, etc.) 2. Patients with preoperative chronic pain 3. Have participated in clinical studies in other projects within 3 months prior to signing the informed consent form 4. subjects not considered by the investigator 5. subjects refused to participate in the study

Design outcomes

Primary

MeasureTime frameDescription
Occurrence of painThe first day to the fifth day after surgery.The NRS scale was used to evaluate the scores.

Secondary

MeasureTime frameDescription
Mastery of the use of patient-controlled analgesia pumpDay 2 after surgeryA series of questions were used to assess patients' mastery of patient-controlled analgesia pump use.

Other

MeasureTime frameDescription
The number of times that the analgesic pump was pressed during each 24h and the amount of analgesic pump remaining at this time were recordedThe first to three days after surgeryThe number of times that the analgesic pump was pressed during each 24h and the amount of analgesic pump remaining at this time were recorded
Patient satisfaction with postoperative analgesiaDay 5 after surgeryPatient satisfaction with postoperative analgesia
The postoperative sleep status of patients was evaluatedThe first day to the fifth day after surgery.The Richards-Campbell Sleep Questionaire Scale was used
The use of rescue analgesics after surgeryThe first day to the fifth day after surgery.Temporary painkillers used in the ward
Adverse events of patients using analgesic pump were recordedThe first day to the fifth day after surgery.Nausea and vomiting, itching, drowsiness, dizziness

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026