This trial is active, not recruiting.

Condition parkinson disease
Treatment tissue implantation
Sponsor National Institute of Neurological Disorders and Stroke (NINDS)
Collaborator University of Colorado, Denver
Start date July 1998
Trial size 40 participants
Trial identifier NCT00004844, 199/13940, UCHSC-COMIRB-9397



I. Assess the safety and efficacy of embryonic mesencephalic dopamine cell implants into the putamen of patients with Parkinson's disease.

United States No locations recruiting
Other countries No locations recruiting

Study Design

Allocation randomized
Endpoint classification safety/efficacy study
Masking double-blind
Primary purpose treatment

Eligibility Criteria

Male or female participants from 40 years up to 75 years old.

PROTOCOL ENTRY CRITERIA: --Disease Characteristics-- - Idiopathic Parkinson's disease for at least 7 years with rest tremor or bradykinesia and one of the following cardinal signs: Rigidity Flexed posture Loss of postural reflexes Freezing (motor blocks) - Continuing response to levodopa - Presence of at least one of the following intractable symptoms or signs: Intractable disabling fluctuations Intractable disabling dyskinesias Intractable "on" freezing (i.e., motor blocks that interfere with walking despite being "on" - Bilateral parkinsonism when "off" (may be asymmetry between right and left sides) - Decreased dopa uptake in the striatum --Prior/Concurrent Therapy-- - No prior brain surgery --Patient Characteristics-- - Cardiovascular: No severe cardiopulmonary disease - Neurologic: No history of strokes No neuroleptics No encephalitis No oculogyric crisis No remission No cerebellar signs No dementia (Mini-Mental state score no greater than 22) No supranuclear gaze palsy No Babinski sign No orthostatic hypotension No hydrocephalus No brain tumor No occlusive cerebrovascular disease - Pulmonary: Absolute standing pressure at least 90/60 mmHg - Other: No diabetes mellitus No exposure to toxins No other severe medical disease Hamilton Depression Scale score of less than 20 points

Additional Information

Description PROTOCOL OUTLINE: This is a randomized, double blind, placebo controlled study. Patients are stratified by age (over and under 60). Patients are randomized to receive either sham surgery or tissue implantation. Embryonic tissue is prepared. While patients are awake, but sedated, bilateral incisions are made in the skin and burr holes drilled in the skull. A cannula is inserted into the brain to the posterior putamen. Implant patients receive embryonic neural tissue or sham patients have no needles penetrate the brain. After 1 year, patients who receive the sham operation in the first operation may receive embryonic neural tissue in a second operation. Patients are followed every 4 months during the first year and every 6 months thereafter.
Trial information was received from ClinicalTrials.gov and was last updated in June 2005.
Information provided to ClinicalTrials.gov by Office of Rare Diseases (ORD).