Pain and Disability Outcomes in Post Amputation Patients
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Limb Pain, Phantom
- Sponsor
- Milton S. Hershey Medical Center
- Enrollment
- 350
- Locations
- 1
- Primary Endpoint
- Change in Pain Severity at rest and movement
- Status
- Recruiting
- Last Updated
- last year
Overview
Brief Summary
The objective of this study is to evaluate efficacy of varied medical and procedural therapies used to treat pain after surgical amputation of a limb. The primary outcome will be assessment of pain severity at rest and with movement as measured by pain scores on Numerical Rating Scale (NRS) 0 to 10, where 0 is not pain and 10 is the worst pain possible, taken on post-operative day 1, day 7, 30 days, 90 days, 6 months, and 1 year (+/- 3 days at each time point).
Detailed Description
The objective of this study is to evaluate efficacy of varied medical and procedural therapies used to treat pain for surgical amputation of a limb. At present there are number of different type of therapies are performed in the patients who is going through an amputation of any limb for management of their pain adequately such as peripheral nerve block, epidurals, peripheral nerve stimulators etc. However, the effects of these different procedures performed at different time intervals have not been evaluated for their effects on phantom pain and somatic pain long term after the procedures in these group of patients. We will be collecting the following data from these patients to see if there is any particular intervention done at particular time of the procedure ( before the amputation vs. after the amputation) affect the long term outcome of these patients such as development of Phantom pain, or chronic pain The primary outcome will be assessment of pain severity at rest and with movement as measured by pain scores on Numerical Rating Scale (NRS) 0 to 10, where 0 is not pain and 10 is the worst pain possible, taken on postoperative day 1, day 7, 30 days, 90 days, 6 months, and 1 year (+/- 3 days at each time point). The secondary outcomes will be 1) phantom limb pain severity as rated on NRS 2) Residual limb (stump) pain as rated on NRS 3) phantom limb sensations 4) Pain Disability Index scores 5) Morphine milligram equivalents. These secondary outcomes will be assessed at the same intervals as the primary outcome. This study will help us to find out if there is any utility of any of these procedures performed at particular time of the procedure helps them more than the others for development of somatic or phantom pain.
Investigators
Sanjib D Adhikary
Professor of Anesthesiology,
Milton S. Hershey Medical Center
Eligibility Criteria
Inclusion Criteria
- •Ages between 18 and 89 years old, inclusive
- •Patients scheduled for surgical limb amputation at Penn State Hershey Medical Center
Exclusion Criteria
- •Patients who cannot cooperate or consent
- •Patients who cannot understand or speak English
- •Patients with a history of chronic regional pain syndromes
- •Patients suffering from alcohol and/or drug abuse -based on previous Dx listed in the MRN
Outcomes
Primary Outcomes
Change in Pain Severity at rest and movement
Time Frame: 1 year
The primary outcome will be assessment of pain severity at rest and with movement as measured by pain scores on Numerical Rating Scale (NRS) 0 to 10 taken on post-operative day 1, day 7, 30 days, 90 days, 6 months, and 1 year (+/- 3 days at each time point). 0 means no pain and 10 means the worst pain ever.
Secondary Outcomes
- Using NRS to rate phantom limb pain change in severity(1 year)
- Using NRS to rate Pain Disabiliy(1 year)
- Using NRS to rate severity of change in pain(1 year)
- Using NRS to rate of change in severity of Phantom limb sensations.(1 year)
- The amount of pain medication used.(1 year)