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Not yet recruitingNCT06327282Updated May 23, 2024

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

An observational study in Postoperative Pain, sponsored by Chinese PLA General Hospital. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-05-23.

Sponsored by Chinese PLA General Hospital · Observational

From the registry’s dates

  • Primary completion was expected by Jan 2025, 1 year 9 months ago, but the record still lists the study as not yet recruiting.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
116
Ages
18 Years and older
Sex
All
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Study summary

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

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Conditions studied

  • Postoperative Pain

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03

In context

Pain, Postoperative

5,093 studies on the registry are indexed under Pain, Postoperative; 1,140 are open to participants now.

This study's planned enrollment of 116 is above the median of 102 across 608 observational studies indexed under Pain, Postoperative.

Browse Pain, Postoperative studies →

Lead sponsor

Chinese PLA General Hospital is the lead sponsor of 558 studies on the registry; 202 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Adult patients undergoing Abdominal Surgery

Inclusion criteria

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

Exclusion criteria

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
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
116 participants (estimated)
Patient registry
No

Groups and cohorts

  • Intervention group

    Anesthesia nurses carried out pain-related knowledge education.

    Behavioral: education on pain and related knowledge

  • Blank group

    Patients who did not receive any knowledge education.

Interventions

  • Behavioraleducation on pain and related knowledge

    Before surgery, pain related knowledge was educated.

    Also known as: pain-related knowledge education

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What researchers measure

Primary outcomes

  1. Occurrence of pain

    The NRS scale was used to evaluate the scores.

    Time frame: The first day to the fifth day after surgery.

Secondary outcomes

  1. Mastery of the use of patient-controlled analgesia pump

    A series of questions were used to assess patients' mastery of patient-controlled analgesia pump use.

    Time frame: Day 2 after surgery

Other outcomes

  1. Patient satisfaction with postoperative analgesia

    Patient satisfaction with postoperative analgesia

    Time frame: Day 5 after surgery

  2. Adverse events of patients using analgesic pump were recorded

    Nausea and vomiting, itching, drowsiness, dizziness

    Time frame: The first day to the fifth day after surgery.

  3. The number of times that the analgesic pump was pressed during each 24h and the amount of analgesic pump remaining at this time were recorded

    The number of times that the analgesic pump was pressed during each 24h and the amount of analgesic pump remaining at this time were recorded

    Time frame: The first to three days after surgery

  4. The use of rescue analgesics after surgery

    Temporary painkillers used in the ward

    Time frame: The first day to the fifth day after surgery.

  5. The postoperative sleep status of patients was evaluated

    The Richards-Campbell Sleep Questionaire Scale was used

    Time frame: The first day to the fifth day after surgery.

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Study locations

No study locations are listed for this record.

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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 23, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06327282
Lead sponsor
Chinese PLA General Hospital
Responsible party
Hao Li (associate chief physician, Chinese PLA General Hospital) — Principal investigator
First posted
Mar 25, 2024
Start date
Jun 15, 2024 (estimated)
Primary completion
Jan 1, 2025 (estimated)
Completion
Apr 4, 2025 (estimated)
Last update
May 23, 2024

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Apr 2024. You cannot join it, but the record below documents what was studied.

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