NCT06327282

Brief Summary

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

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
116

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Jun 2024

Shorter than P25 for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

March 17, 2024

Completed
8 days until next milestone

First Posted

Study publicly available on registry

March 25, 2024

Completed
3 months until next milestone

Study Start

First participant enrolled

June 15, 2024

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2025

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 4, 2025

Completed
Last Updated

May 23, 2024

Status Verified

April 1, 2024

Enrollment Period

7 months

First QC Date

March 17, 2024

Last Update Submit

May 22, 2024

Conditions

Postoperative Pain

Outcome Measures

Primary Outcomes (1)

  • Occurrence of pain

    The NRS scale was used to evaluate the scores.

    The first day to the fifth day after surgery.

Secondary Outcomes (1)

  • Mastery of the use of patient-controlled analgesia pump

    Day 2 after surgery

Other Outcomes (5)

  • Patient satisfaction with postoperative analgesia

    Day 5 after surgery

  • Adverse events of patients using analgesic pump were recorded

    The first day to the fifth day after surgery.

  • 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 first to three days after surgery

  • +2 more other outcomes

Study Arms (2)

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

education on pain and related knowledgeBEHAVIORAL

Before surgery, pain related knowledge was educated.

Also known as: pain-related knowledge education
Intervention group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

Adult patients undergoing Abdominal Surgery

You may qualify if:

  • voluntary informed consent;
  • age older than 18 years
  • abdominal surgery under elective general anesthesia

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Pain, Postoperative

Condition Hierarchy (Ancestors)

Postoperative ComplicationsPathologic ProcessesPathological Conditions, Signs and SymptomsPainNeurologic ManifestationsSigns and Symptoms

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
associate chief physician

Study Record Dates

First Submitted

March 17, 2024

First Posted

March 25, 2024

Study Start

June 15, 2024

Primary Completion

January 1, 2025

Study Completion

April 4, 2025

Last Updated

May 23, 2024

Record last verified: 2024-04

Data Sharing

IPD Sharing
Will not share