TEMporal PostOperative Pain Signatures
Status: | Recruiting |
---|---|
Conditions: | Post-Surgical Pain |
Therapuetic Areas: | Musculoskeletal |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 2/3/2019 |
Start Date: | August 2015 |
End Date: | March 2020 |
Contact: | Judith M Wishin, BSN |
Email: | jwishin@anest.ufl.edu |
Phone: | 352-273-9096 |
Finding Good TEMporal PostOperative Pain Signatures (TEMPOS)
The purpose of this research study is to determine what causes pain after surgery to increase
or decrease over time.
or decrease over time.
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.
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.
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
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