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Completed

NCT Number: NCT00038116

Embryonic Dopamine Cell Implants for Parkinson's Disease

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.

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Key information

Age range

20 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

University Hospital, the University of Colorado Health Sciences Center, Denver, Colorado, United States

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About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

embryonic dopamine cell implant surgery

Procedure

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

Procedure

sham surgery

Primary outcomes

  1. a subjective Global Rating Scale

    Time frame: duration of the trial

Secondary outcomes

  1. objective measurements of PD, including UPDRS motor "off", Schwab and England "off", and 19F-fluorodopa uptake

    Time frame: duration of the trial

Sponsors and collaborators

Lead sponsor

University of Colorado, Denver

Other

Registry information

Official study title

Embryonic Dopamine Cell Implants for Parkinson's Disease: A Double-Blind Study

Important dates

Study start
1995
Primary completion
2009
Study completion
2009
First posted
May 30, 2002
Registry last updated
Feb 5, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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