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NCT01477502 Clinical Trial

Clinical Value of Homeopathic Prophylaxis of Recurrent Urinary Tract Infections in Persons With Spinal Cord Injury

Spinal Cord Injury Clinical Trial

Official title:
Clinical Value of Homeopathic Assessment and Treatment for Prophylaxis of Recurrent Urinary Tract Infections in Persons With Spinal Cord Injury

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01477502
Other study ID # 2011-24
Secondary ID 11050
Status Completed
Phase N/A
First received
Last updated
Start date November 2011
Est. completion date October 2016

Study information
Verified date February 2024
Source Swiss Paraplegic Research, Nottwil
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

recurrent symptomatic urinary tracts infections (UTI) in persons with spinal cord injury are a frequent problem, leading to significant morbidity and to a decreased quality of life. - until today, there is no effective prophylaxis for UTI for patients with spinal cord injury. - homeopathy has been shown to be an effective treatment option in several chronic diseases - study hypothesis: the addition of homeopathic assessment and treatment to a standard prevention strategy for recurrent UTI will significantly reduce the number of symptomatic UTI per year in this group of patients compared to standard prevention alone

Recruitment information / eligibility
Status Completed
Enrollment 46
Est. completion date October 2016
Est. primary completion date August 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - neurogenic bladder dysfunction treated by intermittent catheterization - recurrent (>3/year) symptomatic urinary tract infections Exclusion Criteria: - inability to speak German - already under homeopathic treatment

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• individual homeopathic treatment
participants are diagnosed by a trained homeopath and receive individualized homeopathic treatment in addition to standard UTI prophylaxis
• standard treatment without homeopathy
participants receive standard UTI prophylaxis

Locations
Country Name City State
Switzerland Swiss Paraplegic center Nottwil Lucerne

Sponsors (1)
Lead Sponsor Collaborator
Swiss Paraplegic Research, Nottwil

Country where clinical trial is conducted

Switzerland, 

Outcome
Type Measure Description Time frame Safety issue
Primary number of symptomatic urinary tract infections one year
Secondary number of symptomatic urinary tract infections compared to the previous year one year
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