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Administrative data

NCT number NCT01313819
Other study ID # H-1012-044-344
Secondary ID
Status Unknown status
Phase Phase 4
First received March 10, 2011
Last updated November 9, 2011
Start date April 2011
Est. completion date December 2011

Study information

Verified date November 2011
Source Seoul National University Hospital
Contact Beom S Jeon, MD, PhD
Phone 82-2-2072-2876
Email brain@snu.ac.kr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Tp determine the effect of IV amantadine on dopaminergic-drug-resistant freezing of gait(FOG)in patients with Parkinson`s disease


Description:

1. Freezing of gait (FOG) is one of the most disabling symptoms of Parkinson`s disease.

We experienced that severe FOG was markedly improved by IV amantadine in the patients who had Parkinson`s disease. But IV drug may have placebo effect. Therefore, We designed double blind, placebo controlled study to know whether IV amantadine is effective in the patient with dopaminergic-drug-resistant freezing of gait(FOG).

2. Cross over study design

- Compare the change of FOGQ(freezing of gait questionaire) score from the baseline to IV amantadine and placebo drug

- randomized assigned order of amantadine and placebo drug.

- investigator of FOG: blinded to the order of drugs

- each patient has IV drug for 2 days for each drug


Recruitment information / eligibility

Status Unknown status
Enrollment 20
Est. completion date December 2011
Est. primary completion date December 2011
Accepts healthy volunteers No
Gender All
Age group 30 Years to 80 Years
Eligibility Inclusion Criteria

- age: 30-80 years

- idiopathic Parkinson's disease

- The patient must be taking optimised levodopa/DDI therapy (based on investigator's judgement) during OPD observation period, though the patient have FOG-Q score = 10 points even though On-state.

Exclusion Criteria:

- "Off" freezing:The patient has improved FOG in "On" state

- clinically significant or unstable medical or surgical condition

- The patient has Parkinson plus like MSA, PSP, and PPFG, and secondary parkinsonism like NPH, vascular parkinsonism, postencephalitic parkinsonism, CO poisoning.

- history of seizure.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
PK-Merz® 200mg/500ml inj(Amantadine) , Normal saline 500ml inj
IV amantadine at 200 mg in 500 cm3 of saline solution or normal saline 500 cm3 given over a 3-h period, twice a day for 2 days along with the pre-existing dopaminergic and non-dopaminergic medication

Locations

Country Name City State
Korea, Republic of Seoul National University Hospital Seoul

Sponsors (1)

Lead Sponsor Collaborator
Seoul National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

References & Publications (2)

Giladi N, Kao R, Fahn S. Freezing phenomenon in patients with parkinsonian syndromes. Mov Disord. 1997 May;12(3):302-5. — View Citation

Giladi N. Medical treatment of freezing of gait. Mov Disord. 2008;23 Suppl 2:S482-8. doi: 10.1002/mds.21914. Review. Erratum in: Mov Disord. 2008 Aug 15;23(11):1639-40. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary change of FOGQ score 2 days for each drug
Secondary UPDRS and HY stage 2 days for each drug
Secondary side effect 2 days, 2 weeks after discharge
Secondary Patient global impression 2 days, 2 weeks after discharge
Secondary 4*10m walk test 2 days for each drug
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