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Somato-sensory Reflex Arch in Spinal Cord Injury - Effect on Clinical Outcome

NCT01241630 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 10

Last updated 2014-05-12

No results posted yet for this study

Summary

Spinal cord injury (SCI) usually affects young people and causes severe bowel and bladder dysfunction. Recently, the concept of a surgically created somat-sensory reflex arch for bladder dysfunction in SCI has been introduced. The concept is promising, not just for bladder but also for bowel dysfunction. However, well designed studies need to be performed before recommending the procedure to a large number of patients worldwide. In this study we perform multidisciplinary studies providing necessary information about the clinical outcome of the somato-sensory reflex arch in adult SCI patients.

The hypothesis is as follows:

1. In a "western setting" the somato-sensory reflex arch can be created in adult SCI patients with only minor morbidity and complications.
2. Somato-sensory reflex arch reduces bladder and bowel symptoms in SCI patients.

Conditions

  • Spinal Cord Injury

Interventions

PROCEDURE

Somatosensory reflex arch (Xiao Procedure)

Cross over surgery. Proximal part of L5 Ventral root is anastomosed to distal part of ventral root of S2 or S3 producing a somato-sensory reflex arch

Sponsors & Collaborators

  • Lundbeck Foundation

    collaborator OTHER

  • University of Aarhus

    lead OTHER

Principal Investigators

  • Klaus Krogh, MD,PhD, DmSc · Aarhus University Hospital

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-11-30
Primary Completion
2013-09-30
Completion
2013-09-30

Countries

  • Denmark

Study Locations

More Related Trials

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 NCT01241630 on ClinicalTrials.gov