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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01010919
Other study ID # PMI-005-01
Secondary ID
Status Completed
Phase Phase 1
First received November 6, 2009
Last updated November 9, 2009

Study information

Verified date November 2009
Source Phytomedics Inc.
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

Extracts of chicory root have anti-inflammatory properties in vitro and in animal models of arthritis. The primary objective of this investigator-initiated, Phase 1, placebo-controlled, double blind, dose-escalating trial is to determine the safety and tolerability of a proprietary bioactive extract of chicory root in patients with osteoarthritis (OA). Secondary objectives are to assess effects on the signs and symptoms of this disorder. Individuals greater than 50 years of age with OA of the hip or knee will be eligible for trial entry.


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender Both
Age group 50 Years and older
Eligibility Inclusion Criteria:

1. Patients must be 50 years of age or older and may be of either gender.

2. Patients must have have an imaging-confirmed (radiograph or MRI) diagnosis of OA of the hip or knee.

3. Patients must not have taken a nonsteroidal anti-inflammatory medication for at least 7 days prior to the baseline visit (a single daily aspirin 325 mg or less is allowed throughout the study).

4. Patients must be able and willing to give informed consent.

Exclusion Criteria:

1. Any unstable comorbid medical condition that in the opinion of the investigator could interfere with the ability of the patient to complete the study.

2. Patients who are unable to ambulate and require a wheelchair due to the severity of the arthritis are excluded. Ambulatory aids such as canes and walkers are acceptable.

3. Patients requiring continuing therapy with nonsteroidal anti-inflammatory drugs are excluded.

4. Patients requiring any dose of glucocorticoids within the past 30 days are excluded.

Study Design

N/A


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Chicory root extract


Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Phytomedics Inc. University of Texas, Southwestern Medical Center at Dallas
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