Status:
COMPLETED
Clinical Trial of Remote Preconditioning in Patients Undergoing Cervical Decompression Surgery
Lead Sponsor:
Xijing Hospital
Conditions:
Cervical Compression Myelopathy
Ischemia
Eligibility:
All Genders
30-75 years
Phase:
PHASE1
PHASE2
Brief Summary
The purpose of this study is to assess whether a large clinical trial testing the effect of RIPC on neurologic outcome in patients undergoing elective cervical decompression surge is warranted.
Detailed Description
Spinal cord ischemia-reperfusion injury commonly contribute to perioperative morbidity and mortality after elective cervical decompression surgery.Remote ischemic preconditioning(RIPC)is a phenomenon ...
Eligibility Criteria
Inclusion
- Patients with clinical and radiological signs of cervical compression myelopathy(ccm)
- Age 30-75
- Stage 1-2
Exclusion
- Age\>75
- History of heart,hepatic,renal or pulmonary disease.
- History of peripheral vascular disease affecting the upper limbs.
Key Trial Info
Start Date :
September 1 2007
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
April 1 2009
Estimated Enrollment :
51 Patients enrolled
Trial Details
Trial ID
NCT00778323
Start Date
September 1 2007
End Date
April 1 2009
Last Update
February 25 2011
Active Locations (1)
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1
Xijing Hospital
Xi'an, Shaanxi, China, 710032