Gainesville, Florida 32610


Purpose:

The purpose of this research study is to determine what causes pain after surgery to increase or decrease over time.


Study summary:

Before surgery, study participants will be asked questions about age, gender, race/ethnicity, annual income, and education level. Study participants will also be questioned regarding prior pain experiences, their mood and how they think about pain. A small test tube of blood, a cheek swab or a saliva sample will be taken to see what genetic differences may influence individuals pain after surgery. After surgery, study participants will be asked questions about their pain intensity while in the hospital. Additional information will be collected about the effects of pain medicine, and their recovery from surgery. Following discharge from the hospital, study participants will be contacted monthly to confirm continued communication. Study participants will also be contacted six months after surgery, and asked to complete a final survey about their pain after surgery.


Criteria:

Inclusion Criteria: - 18 years of age or older - anticipated length of hospital stay of 72 hours or greater - expected post-operative survival greater than 6 months Exclusion Criteria: - < 18 years of age - anticipated need for prolonged post-operative intubation (greater than 24 hours) - urgent or emergent surgical procedure - inability to understand or participate in questionnaires, surveys or data collection


NCT ID:

NCT02407743


Primary Contact:

Principal Investigator
Patrick J Tighe, MD
Assistant Professor of Anesthesiology and Program Director, Perioperative Analytics Group Joint Assi

Judith M Wishin, BSN
Phone: 352-273-9096
Email: jwishin@anest.ufl.edu


Backup Contact:

N/A


Location Contact:

Gainesville, Florida 32610
United States

Judith M Wishin, BSN
Phone: 352-494-3165

Site Status: Recruiting


Data Source: ClinicalTrials.gov

Date Processed: November 19, 2017

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


Click to view Full Listing

If you would like to be contacted by the clinical trial representative please fill out the form below.