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Clinical Trial of Remote Preconditioning in Patients Undergoing Cervical Decompression Surgery

NCT00778323 · Status: COMPLETED · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 51

Last updated 2011-02-25

No results posted yet for this study

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.

Conditions

  • Cervical Compression Myelopathy
  • Ischemia
  • Reperfusion Injury
  • Spinal Cord Injury

Interventions

PROCEDURE

limb remote ischemic preconditioning (LRIPC)

LRIPC consists of three 5-min cycles of right upper limb ischemia induced by an automated cuff-inflator placed on the upper arm and inflated to 200 mmHg,with an intervening 5 min reperfusion during which the cuff is deflated.

Sponsors & Collaborators

  • Xijing Hospital

    lead OTHER

Principal Investigators

  • Lize Xiong, MD · Xiling Hospital,Fourth Military Medical University

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
30 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-09-30
Primary Completion
2008-10-31
Completion
2009-04-30

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00778323 on ClinicalTrials.gov