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

Postoperative Pain Clinical Trial

Official title:

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

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06327282
• Other study ID #: ChinaPLAGHPAIN
• Status: Not yet recruiting
• Start date: May 1, 2024
• Est. completion date: April 4, 2025

Study information

• Verified date: April 2024
• Source: Chinese PLA General Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

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

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 116
• Est. completion date: April 4, 2025
• Est. primary completion date: January 1, 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Pain, Postoperative
• Postoperative Pain

Intervention

Behavioral:
• education on pain and related knowledge
Before surgery, pain related knowledge was educated.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Chinese PLA General Hospital

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Patient satisfaction with postoperative analgesia	Patient satisfaction with postoperative analgesia	Day 5 after surgery
Other	Adverse events of patients using analgesic pump were recorded	Nausea and vomiting, itching, drowsiness, dizziness	The first day to the fifth day after surgery.
Other	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	The first to three days after surgery
Other	The use of rescue analgesics after surgery	Temporary painkillers used in the ward	The first day to the fifth day after surgery.
Other	The postoperative sleep status of patients was evaluated	The Richards-Campbell Sleep Questionaire Scale was used	The first day to the fifth day after surgery.
Primary	Occurrence of pain	The NRS scale was used to evaluate the scores.	The first day to the fifth day after surgery.
Secondary	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.	Day 2 after surgery