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NCT03307525 Clinical Trial

Pain After Breast Surgery

Breast Cancer Clinical Trial

Official title:
A Pilot Study Assessing the Correlation of Preoperative Sensory Testing and Genetic Polymorphisms With Acute and Persistent Postoperative Pain

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT03307525
Other study ID # Pro00026402
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 20, 2012
Est. completion date December 22, 2015

Study information
Verified date October 2017
Source Duke University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This is a pilot observational study assessing various predictors for acute pain and persistent pain following breast surgery for cancer.

Recruitment information / eligibility
Status Completed
Enrollment 141
Est. completion date December 22, 2015
Est. primary completion date December 22, 2015
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: - English speaking undergoing elective breast cancer surgery Exclusion Criteria: - Patients with recurrent cancer, metastasis, and previous breast surgery

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
n/a

Sponsors (2)
Lead Sponsor Collaborator
Duke University Society for Ambulatory Anesthesia (SAMBA)

Outcome
Type Measure Description Time frame Safety issue
Primary Acute Pain Maximum pain score reported postoperatively 72 hours after surgery
Secondary Persistent Pain pain score = 3 or pain that impacts daily life as indicated by a score >0 on any of the 7 daily activity questions more than 6 months after surgery More than 6 months after surgery
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