Safety and Efficacy Study of Bee Venom to Treat Knee Osteoarthritis
NCT ID: NCT00253942
Last Updated: 2005-11-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
PHASE3
40 participants
INTERVENTIONAL
2005-11-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Injecting bee venom as a treatment for OA
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Morning stiffness less than 30 minutes duration
* VAS pain level of 4 to 8 on a 0 to 10 scale when walking
* Older than 35 years of age
* On a stable dose of medication or none at all due to intolerance
* Ability to tolerate Acetaminophen as their only pain medication for the entire study
* Ability to read, understand, and give informed consent and sign the informed consent form
Exclusion Criteria
* Allergy to Lidocaine
* Any type of inflammatory arthritis such as RA, SLE, Psoriatic
* Fibromyalgia or any pain problem that requires the use of pain medication or anti-inflammatory
* Depression or any condition that interferes with memory or critical analysis
* History of prolotherapy, bee venom therapy, or injection of hyaluronic acid or cortisone within the last 3 months
* Osteoarthritis of the hip, ankle, or any condition that interferes with walking 50 ft. or up and down stairs
* Elevated CRP, SED rate
* Recent injury to the knee which is causing pain or functional problems
* Any previous invasive procedure on the study knee
* Inability to understand the informed consent form or refusal to sign it
* Cardiac disease interfering with ability to get epinephrine
* VAS pain level greater than 8 on a 0 to 10 scale when walking
* Inability to stop anti-inflammatory medication for the entire study and use only Acetaminophen
* Taking beta blockers
* Taking chronic anti-histamines
35 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Kochan Institute for Healing Arts Research
UNKNOWN
Rheumatology Therapeutics Medical Center
OTHER
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Boris Ratiner, MD
Role: PRINCIPAL_INVESTIGATOR
Medical Director of Rheumatology Therapeutics Medical Center
Andrew Kochan, MD
Role: PRINCIPAL_INVESTIGATOR
Medical Director of Kochan Institute for Healing Arts Research
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Kochan Institute for Healing Arts Research
Encino, California, United States
Rheumatology Therapeutics Medical Center
Tarzana, California, United States
Countries
Review the countries where the study has at least one active or historical site.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Ray Seipel, MA
Role: primary
Phil Sheng, BS
Role: primary
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
OABVTKNEE-001
Identifier Type: -
Identifier Source: org_study_id