Embryonic Dopamine Cell Implants for Parkinson's Disease
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Purpose
The purpose of this trial is to determine if patients who received embryonic dopamine cell implant surgery showed significantly greater improvement in their Parkinson's disease than a control group undergoing the placebo treatment, and to determine if the cell implant surgery was more effective in younger or older patients.
| Condition | Intervention | Phase |
|---|---|---|
|
Parkinson Disease |
Procedure: embryonic dopamine cell implant surgery Procedure: placebo |
Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Intervention Model: Crossover Assignment Masking: Double Blind (Subject, Investigator) Primary Purpose: Treatment |
| Official Title: | Embryonic Dopamine Cell Implants for Parkinson's Disease: A Double-Blind Study |
- a subjective Global Rating Scale [ Time Frame: duration of the trial ] [ Designated as safety issue: No ]
- objective measurements of PD, including UPDRS motor "off", Schwab and England "off", and 19F-fluorodopa uptake [ Time Frame: duration of the trial ] [ Designated as safety issue: No ]
| Enrollment: | 40 |
| Study Start Date: | May 1995 |
| Study Completion Date: | August 2009 |
| Primary Completion Date: | August 2009 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Active Comparator: embryonic dopamine cell implant surgery
embryonic dopamine cell implant surgery
|
Procedure: embryonic dopamine cell implant surgery
Half of the participants received the cell implant surgery, while the other half received the placebo. After the double-blind phase of the study, patients in the placebo group had the option of receiving tissue implants. Fourteen of these patients eventually had transplants.
|
|
Placebo Comparator: sham surgery
sham surgery (placebo)
|
Procedure: placebo
sham surgery
|
Detailed Description:
Parkinson's disease is caused by the death of a small number of nerve cells that produce a critical chemical called dopamine. The drug L-dopa can partially make up for the lack of dopamine. As time goes on, however, most patients notice that the drugs do not work as well. Oftentimes, patients develop great fluctuations in motor control. Off drugs they cannot move, and on drugs they have excess, exaggerated movements. Research in animals over the last 20 years has shown that dopamine cells can be replaced by transplants of new cells obtained from fetal brain tissue. For the past 14 years, several laboratories around the world have been performing similar transplants of human fetal brain tissue on patients with Parkinson's disease. So far, it has been impossible to compare results from the different groups because no two centers are performing transplants in the same way.
This study seeks to get around that problem using a controlled clinical trial that compares the embryonic dopamine cell implant surgery with a placebo treatment. A total of 40 patients were recruited--half received the cell implant surgery, while the other half received the placebo. After the double-blind phase of the study, patients in the placebo group had the option of receiving tissue implants. Fourteen of these patients eventually had transplants. At present, this study is providing long-term follow-up evaluation and treatment for the subjects.
Eligibility| Ages Eligible for Study: | 20 Years to 75 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
INCLUSION CRITERIA:
- Idiopathic Parkinson's disease of at least 7 years duration and responsive to levodopa. Other Parkinson syndromes excluded.
- Patients previously tried on other available forms of medical treatment.
- Age between 20 and 75 years.
- Presence of an intractable problem, such as "off" periods, dyskinesias, or "freezing," not controlled by dopamine agonists such as levodopa or pergolide.
- No serious depression and no cognitive impairment.
- Successful completion of home diary by patient or responsible party.
- Successful videotape recordings at home of "on" and "off" status.
- Normal MRI of brain within the last 18 months.
- Fluorodopa PET scan compatible with idiopathic Parkinson's disease.
- Medically fit to undergo implant surgery with certification by the patient's physician.
- Able to financially cover expenses not paid for by NIH grant (between $1,000 and $2,000 for unreimbursed travel, video camera, and blood screening as specified in the consent form.
EXCLUSION CRITERIA:
- Severe or moderately severe depression or cognitive impairment.
- Previous brain surgery.
- Presence of diabetes mellitus, severe cardiopulmonary disease or other severe medical disease, or MRI evidence of cerebrovascular disease.
- Not medically cleared to undergo a surgical procedure.
Contacts and Locations| United States, Colorado | |
| University Hospital, the University of Colorado Health Sciences Center | |
| Denver, Colorado, United States, 80262 | |
| United States, New York | |
| North Shore University Hospital | |
| Manhasset, New York, United States, 11030 | |
| The Movement Disorder Center, Columbia-Presbyterian Hospital | |
| New York, New York, United States, 10032 | |
| Principal Investigator: | Curt R. Freed, M.D. | University of Colorado, Denver |
More Information
Publications:
| Responsible Party: | University of Colorado, Denver |
| ClinicalTrials.gov Identifier: | NCT00038116 History of Changes |
| Other Study ID Numbers: | 93-0097 |
| Study First Received: | May 29, 2002 |
| Last Updated: | February 4, 2013 |
| Health Authority: | United States: Federal Government |
Keywords provided by University of Colorado, Denver:
|
Parkinson's disease PD dopamine embryonic dopamine cell implant surgery tissue implants |
Additional relevant MeSH terms:
|
Parkinson Disease Parkinsonian Disorders Basal Ganglia Diseases Brain Diseases Central Nervous System Diseases Nervous System Diseases Movement Disorders Neurodegenerative Diseases Dopamine Dopamine Agents Cardiotonic Agents |
Cardiovascular Agents Therapeutic Uses Pharmacologic Actions Sympathomimetics Autonomic Agents Peripheral Nervous System Agents Physiological Effects of Drugs Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action Protective Agents |
ClinicalTrials.gov processed this record on June 18, 2013