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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02138149
Other study ID # 2013-22
Secondary ID
Status Completed
Phase N/A
First received May 12, 2014
Last updated November 16, 2015
Start date November 2013
Est. completion date November 2015

Study information

Verified date November 2015
Source Swiss Paraplegic Centre Nottwil
Contact n/a
Is FDA regulated No
Health authority Switzerland: Federal Office of Public Health
Study type Observational

Clinical Trial Summary

Spinal cord injury (SCI) almost always affects bladder function as well. As a result of this bladder dysfunction, individuals with SCI have to undergo regular invasive examination of their bladder function (urodynamic examination).

The nerve growth factor (NGF) is released from smooth muscle cells of the bladder, and there are reports, that the concentration of NGF is elevated in the urine of patients with bladder dysfunction. The NGF concentration can also be measured in the blood. The concentration of NGF in the blood and urine of SCI individuals has not yet been investigated. These concentrations may correlate with the severity of bladder dysfunction, and may thus be used to replace or at least reduce the number of the more invasive urodynamic examinations.

The hypothesis that urine and blood NGF concentrations in individuals with SCI are higher compared to individuals with healthy bladder function will be tested.


Recruitment information / eligibility

Status Completed
Enrollment 47
Est. completion date November 2015
Est. primary completion date November 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 80 Years
Eligibility Control Group

Inclusion Criteria:

- physiologic bladder function

Exclusion Criteria:

- no signed consent form

- age <18 / >80 years

- urinary tract infection

- bladder surgery

- radiation therapy of the pelvic area

- pregnancy

- bleeding disorder

Study Group

Inclusion Criteria:

- neurogenic detrusor overactivity

- presentation for urodynamic examination

Exclusion Criteria:

- no signed consent form

- age <18 / >80 years

- urinary tract infection

- bladder augmentation

- bladder evacuation by permanent catheterization

- radiation therapy of the pelvic area

- pregnancy

- bleeding disorder

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Switzerland Swiss Paraplegic Centre Nottwil LU

Sponsors (1)

Lead Sponsor Collaborator
Swiss Paraplegic Centre Nottwil

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary urinary concentration of nerve growth factor day 0 No
Secondary serum concentration of nerve growth factor day 0 No
Secondary demographics day 0 No
Secondary urodynamics only participants with spinal cord injury day 0 No
Secondary International Prostate Symptom Score (I-PSS) day 0 No
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