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NCT01893619 Clinical Trial

Observational Research on Use of Immunoprop Supplement in Chronic Fatigue Syndrome

Chronic Fatigue Syndrome Clinical Trial

— immunoprop  

Official title:
Observational Research on Use of Immunoprop Supplement in Chronic Fatigue Syndrome

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT01893619
Other study ID # immunoprop
Secondary ID
Status Recruiting
Phase N/A
First received July 2, 2013
Last updated July 24, 2013
Start date June 2013
Est. completion date December 2013

Study information
Verified date July 2013
Source New York CFS Association
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Observational

Clinical Trial Summary

Observational study regarding the use of supplements in chronic fatigue syndrome patients

Description:

Detailed questionnaire regarding the diagnosis of an onset of chronic fatigue syndrome and 100 patients. using Karnofsky scale before and after use of supplements patient scores are compared in a double blind trial.

Recruitment information / eligibility
Status Recruiting
Enrollment 100
Est. completion date December 2013
Est. primary completion date December 2013
Accepts healthy volunteers No
Gender Both
Age group 21 Years to 60 Years
Eligibility Inclusion Criteria:

- Fukuda criteria and Canadian consensus criteria will be the diagnosis criteria for patient selection

Exclusion Criteria:

- non inclusion in the above criteria

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
United States Me/Cfs Center,860 Fifth Avenue New York New York

Sponsors (1)
Lead Sponsor Collaborator
New York CFS Association

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Karnovsky score comparison Review of Karnofsky score over prior to diagnosis and subsequent to patients having taken supplements Six months No
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