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Clinical Trials/NCT00778323
NCT00778323
Completed
Phase 1

Effects of Remote Ischemic Preconditioning on Biochemical Markers and Neurological Outcomes in Patients Undergoing Elective Cervical Decompression Surgery

Xijing Hospital1 site in 1 country51 target enrollmentSeptember 2007

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Cervical Compression Myelopathy
Sponsor
Xijing Hospital
Enrollment
51
Locations
1
Primary Endpoint
serum concentrations of s-100B,NSE
Status
Completed
Last Updated
15 years ago

Overview

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 whereby brief periods of ischemia followed by reperfusion in one organ provide system protection from prolonged ischemia.The hypothesis of this protocol is that limb ischemic preconditioning could reduces spinal cord ischemia-reperfusion injury induced by elective cervical decompression surgery.Serum s-100B and NSE concentration will be measured before and after induction ,and at 6 hours,1,3,5 and 7days after surgery.JOA scores in all the cases will be evaluated before operation and at 7days ,1,3,6 month after surgery.

Registry
clinicaltrials.gov
Start Date
September 2007
End Date
April 2009
Last Updated
15 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Xijing Hospital

Eligibility Criteria

Inclusion Criteria

  • Patients with clinical and radiological signs of cervical compression myelopathy(ccm)
  • Age 30-75
  • Stage 1-2

Exclusion Criteria

  • History of heart,hepatic,renal or pulmonary disease.
  • History of peripheral vascular disease affecting the upper limbs.

Outcomes

Primary Outcomes

serum concentrations of s-100B,NSE

Time Frame: 1 week or more

Secondary Outcomes

  • a Japanese Orthopaedic Association (JOA) scale(6 months)

Study Sites (1)

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