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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03021447
Other study ID # AJIRB-MED-OBS-16-48
Secondary ID
Status Not yet recruiting
Phase N/A
First received January 12, 2017
Last updated January 13, 2017
Start date January 2017
Est. completion date December 2017

Study information

Verified date January 2017
Source Ajou University School of Medicine
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Postoperative pain is a significant postoperative problem and it could be persistent if proper management is not provided. However, each patient shows different intensity of pain and different sensitivity to analgesics even if they underwent same procedures. Therefore, it would be useful to find the way to predict the postoperative pain sensitivity.

Propofol, a popular anesthetic agent, induces pain during injection, which can not completely prevented by opioid or lidocaine in some patients. This is considered to be related to patient's pain sensitivity and it might be associated with postoperative pain sensitivity.

Therefore, the relation of propofol injection pain and postoperative pain intensity will be explored.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 70
Est. completion date December 2017
Est. primary completion date December 2017
Accepts healthy volunteers No
Gender Female
Age group 19 Years to 60 Years
Eligibility Inclusion Criteria:

- America Society of Anesthesiologists class I-II

- Laparoscopic cholecystectomy

Exclusion Criteria:

- Pregnancy

- Illiteracy

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Ajou University School of Medicine

Outcome

Type Measure Description Time frame Safety issue
Primary postoperative pain intensity_1 Postoperative pain will be evaluated with verbal numeric scale (0-10) 10 min after postanesthesia care unit admission
Secondary postoperative pain intensity_2 Postoperative pain will be evaluated with verbal numeric scale (0-10) 20 min after postanesthesia care unit admission
Secondary postoperative pain intensity_3 Postoperative pain will be evaluated with verbal numeric scale (0-10) 30 min after postanesthesia care unit admission
Secondary postoperative pain intensity_4 Postoperative pain will be evaluated with verbal numeric scale (0-10) 4 hours after operation
Secondary postoperative pain intensity_8 Postoperative pain will be evaluated with verbal numeric scale (0-10) 8 hours after operation
Secondary postoperative pain intensity_12 Postoperative pain will be evaluated with verbal numeric scale (0-10) 12 hours after operation
Secondary postoperative pain intensity_24 Postoperative pain will be evaluated with verbal numeric scale (0-10) 24 hours after operation
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