Clinical Trials Directory

Trials / Terminated

TerminatedNCT00638404

Severity Postoperative Pain Prediction

Predicting Severity of Postoperative Pain After Surgery

Status
Terminated
Phase
Study type
Observational
Enrollment
300 (actual)
Sponsor
Wake Forest University · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

A simple preoperative evaluation assessing level of anxiety, anticipated pain, and intensity rating of audio tone will predict the severity of postoperative pain after surgery.

Detailed description

The purpose of this study would be to determine the predictive value of a simple to perform preoperative evaluation in assessing level of anxiety, anticipated pain and the intensity rating of an audio tone to predict level of postoperative pain after surgery. Study Design: A total of 400 evaluable patients will be studied using the various surgical populations listed. For statistical purposes, the following will be the surgical population by procedure. Two hundred healthy ASA I-II women scheduled for elective cesarean section, one hundred scheduled for elective postpartum tubal ligations, and one hundred scheduled for elective inpatient gynecological surgeries (such as total vaginal hysterectomy, total abdominal hysterectomy) will be consented and enrolled in the study. Normal baseline vital signs will be obtained and recorded as part of usual preoperative assessment for these patients. The patients will be asked about their current level of pain and to rate the intensity of a series of audio tones. At 18-24 hours postoperatively, and again at 36-48 hours postoperatively if applicable, research personnel will evaluate the severity of postoperative pain the patient has at rest and with movement (from supine to sitting upright), using a sliding pain scale from 0 to 100 mm, with 0 being no pain and 100 being the worst pain ever. Information on drug administered in the preoperative, intraoperative and postoperative period will be collected and recorded. The subject can also choose to allow us to follow-up with them in the future to evaluate current residual postoperative pain levels as needed.

Conditions

Timeline

Start date
2007-08-01
Primary completion
2009-09-01
Completion
2009-09-01
First posted
2008-03-19
Last updated
2018-08-06
Results posted
2018-08-06

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00638404. Inclusion in this directory is not an endorsement.