Predicting Acute Postoperative Pain by the Preoperative Lower Back Pain

Benign Gynecological Disease Clinical Trial

Official title:

Predicting Acute Postoperative Pain by the Preoperative Lower Back Pain in the Gynecological Laparoscopy

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04793191
• Other study ID #: back pain
• Status: Completed
• Start date: March 20, 2021
• Est. completion date: February 15, 2022

Study information

• Verified date: March 2021
• Source: The Catholic University of Korea
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

To investigate if the level of preoperative lower back pain has the effect on the acute postoperative pain after gynecological laparoscopy

Recruitment information / eligibility

• Status: Completed
• Enrollment: 150
• Est. completion date: February 15, 2022
• Est. primary completion date: January 31, 2022
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 20 Years to 65 Years

Eligibility

Inclusion Criteria:

• women scheduled for elective gynecological laparoscopy

Exclusion Criteria:

• psychiatric disease eg. anxiety, depression, etc.

• diagnosed as cancer

• the use of vasoactive drug

• chronic pain except lower back pain

Related Conditions & MeSH terms

• Back Pain
• Benign Gynecological Disease
• Low Back Pain
• Pain, Postoperative

Locations

Country	Name	City	State
Korea, Republic of	Seoul St.Mary's Hospital	Seoul	Seocho-gu

Sponsors (1)

Lead Sponsor	Collaborator
The Catholic University of Korea

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	the intensity of acute postoperative pain	The intensity of pain is assessed using the numeric rating scale (0=no pain; 10=the worst pain)	during 30 min in the recovery room