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NCT02529943 Clinical Trial

Changes in Motor Latency During Spinal Decompression: Relationship to Outcomes

Spinal Stenosis Clinical Trial

Official title:
Changes in Motor Latency During Spinal Decompression: Relationship to Outcomes

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02529943
Other study ID # Norton15_05
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 2016
Est. completion date May 1, 2022

Study information
Verified date May 2022
Source University of Saskatchewan
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Is there a relationship between changes in motor evoked potential latency intraoperatively and post-operative changes in walking function in patients undergoing spinal decompression.

Description:

Is there a relationship between changes in motor evoked potential latency intraoperatively and post-operative changes in walking function in patients undergoing spinal decompression. Tests will include the pre and post decompression MEP (motor evoked potential) latency and pre and post surgery walking speed and quality of life assessments.

Recruitment information / eligibility
Status Completed
Enrollment 25
Est. completion date May 1, 2022
Est. primary completion date October 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Central spinal stenosis - Ability to ambulate prior to onset of symptoms Exclusion Criteria: - Arthritis affecting walking ability (hip, knee or ankle). - Diabetes - Implanted pacemaker or other electrostimulator.

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Canada Royal University Hospital Saskatoon Saskatchewan

Sponsors (1)
Lead Sponsor Collaborator
University of Saskatchewan

Country where clinical trial is conducted

Canada, 

Outcome
Type Measure Description Time frame Safety issue
Primary Motor Evoked Potential Latency MEP latency at induction and completion of decompression Day 0
Secondary 10 m Timed Walking speed 10m timed walk pre-surgery and 3 months post surgery
Secondary Quality of Life measured in SF-36 SF-36 pre-surgery and 3 months post surgery
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