- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01893619
Observational Research on Use of Immunoprop Supplement in Chronic Fatigue Syndrome (immunoprop)
July 24, 2013 updated by: New York CFS Association
Observational study regarding the use of supplements in chronic fatigue syndrome patients
Study Overview
Status
Unknown
Conditions
Detailed 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.
Study Type
Observational
Enrollment (Anticipated)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
New York
-
New York, New York, United States, 10065
- Recruiting
- Me/Cfs Center,860 Fifth Avenue
-
Contact:
- derek enlander, MD
- Phone Number: 212-794-2000
- Email: denlander@aol.com
-
Principal Investigator:
- derek enlander, md
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
21 years to 60 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Fukuda criteria and Canadian consensus criteria will be the diagnosis criteria for patient selection
Description
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 Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Karnovsky score comparison
Time Frame: Six months
|
Review of Karnofsky score over prior to diagnosis and subsequent to patients having taken supplements
|
Six months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: DEREK enlander, CFIDS RESEARCH FOUNDATION
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
June 1, 2013
Primary Completion (Anticipated)
December 1, 2013
Study Completion (Anticipated)
December 1, 2013
Study Registration Dates
First Submitted
July 2, 2013
First Submitted That Met QC Criteria
July 8, 2013
First Posted (Estimate)
July 9, 2013
Study Record Updates
Last Update Posted (Estimate)
July 25, 2013
Last Update Submitted That Met QC Criteria
July 24, 2013
Last Verified
July 1, 2013
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- immunoprop
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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