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Clinical study of selegiline hydrochloride ( FP OD tablet 2.5) to flexion of spine in Parkinson's disease.

Clinical study of selegiline hydrochloride ( FP OD tablet 2.5) to flexion of spine in Parkinson's disease. - Clinical study of selegiline to flexion of spine in Parkinson's disease.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000008477
Enrollment
20
Registered
2012-07-19
Start date
2012-07-19
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Parkinson disease

Interventions

Selegiline hydrochloride 5mg 8weeks, 7.5mg 8weeks and stop it, followed after 8weeks, and evaluate each points.

Sponsors

Department of Neurology, Juntendo Koshigaya Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients diagnosed as Parkinson' s disease and classified into Modified Hohen & Yahr staging Scale I through 2) Patients whose symptom of posture disorder is latent in supine position 3) Patients aged 20 or over when their consents given 4) Hospitalized patients/outpatients

Exclusion criteria

Exclusion criteria: 1) Patients receiving drugs prohibited for concomitant 2) Patients who have lumber spine deformation evaluated by an X-ray examination 3) Patients whit orthostatic hypotension 4) Patients receiving medical treatment for epilepsy 5) Patient who have symptoms of serious nerve and / or psychiatric disorders such as disturbance of consciousness , hallucination , delusions and abnormal behavior 6) Patient with severs disease of heart , blood vessels , liver , renal , blood and other life-threatening diseases 7) Patients who have or had schizophrenia 8) Patients who have or had addiction to central nerve system stimulants such as cocaine 9) Patients who are pregnant during the period of study 10) Patients addiction to alcohol or drugs 11) Patients who are determined as unfit for the study by attending physicians for reasons other than those stated above

Design outcomes

Primary

MeasureTime frame
Rsults of stabilometry (Gravicoder GS-3000; AeNIMA)

Secondary

MeasureTime frame
1. Modified Hoehn & Yahr stage of Parkinson's Disease 2. Iapanese version, UPDRS Part I, Part II, Part III, Part IV 3. Degree of posture flexion (degree of antero flexion/ degree of side flexion) using photo. 4. Pain evaluation with VAS scale. 5. Safety evaluation, side effects.

Countries

Japan

Contacts

Public ContactAsako Yoritaka

Juntendo Koshigaya Hospital Neurology

ayori@juntendo.ac.jp+81-48-975-0321

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026