Complex Regional Pain Syndrome (CRPS) Clinical Trial
40 CRPS patients will be recruited over a three-year period (target of 160 patients at all sites). Assessment of exclusion criteria will be undertaken during initial recruitment. Exclusion criteria are: <18 years; a second chronic pain syndrome that would interfere with pain rating; psychiatric comorbidity; pain in both hands or feet; pregnancy or breastfeeding; sympathectomy in the affected limb; use of topical medication; known sensitivity to alpha 1- adrenoceptor agonists or other contraindications. Patients will maintain their regular oral medications throughout the study period. Assessment of sympathetically maintained pain (SMP) will require an intradermal dose of Phenylephrine to rekindle SMP and mechanical hyperalgesia. Clonidine will be used to control for affects of algometer fiction and may inhibit SMP by inhibiting the release of more norepinephrine from sympathetic nerve terminals. Skin biopsies will be obtained under sterile conditions from a site of mechanical or thermal hyperalgesia using a 3mm diameter skin biopsy punch under local anesthesia. Samples from a mirror image site on the contralateral body side will also be taken.
Patients diagnosed with CRPS and control subjects will be enrolled in the study. The CRPS participants will be administered with phenylephrine (day 1) and clonidine (day 2). The control participants will not receive any intervention. The aim of this study is to determine if expression of α1-adrenoceptors (α1-AR) altered in the skin of a subgroup of patients whose pain is associated with increased adrenergic sensitivity after nerve trauma. Increased adrenergic sensitivity will be determined by assessing pain in patients after administration of phenylephrine on day 1. Expression of α1-AR will be determined by taking skin biopsies on day 2 after administration of clonidine. Then, we will compare the expression of α1-AR in patients who were classified as having increased adrenergic sensitivity versus those who were not. ;
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT01512121 -
Spinal Cord Stimulation and Functional MRI
|
||
| Completed |
NCT02265848 -
High Frequency Stimulation Trials in Patients With Precision Spinal Cord Stimulator System
|
Phase 4 | |
| Active, not recruiting |
NCT01508676 -
Effects of Pennsaid on Clinical Neuropathic Pain
|
N/A | |
| Terminated |
NCT03560986 -
Efficacy and Safety of Intravenous Neridronic Acid in Complex Regional Pain Syndrome (CRPS)
|
Phase 3 | |
| Terminated |
NCT03530345 -
Efficacy and Safety of Intravenous Neridronic Acid in CRPS
|
Phase 3 | |
| Completed |
NCT03285113 -
A Study to Confirm the Safety of High Frequency DRG Stimulator in Patients With Chronic Lower Limb Pain
|
N/A | |
| Recruiting |
NCT03686748 -
Two Point Discrimination
|
Early Phase 1 | |
| Completed |
NCT01926119 -
TMS for CRPS - Pilot Study
|
N/A | |
| Completed |
NCT02067273 -
Transcranial Magnetic Stimulation (TMS) for CRPS
|
N/A | |
| Completed |
NCT01118988 -
Peer Mentorship: An Intervention To Promote Effective Pain Self-Management In Adolescents
|
N/A | |
| Active, not recruiting |
NCT02800863 -
TARGET Post-Approval Study
|