parkinson'
Conditions
Interventions
we measured smell test and urine 8-OHdG before and after 3.5% hydrogen gas. After two month discontinuation of administration. we measured smell test and urine 8-OHdG before and after room air.
we me
Sponsors
Nagoya University Graduate School of Medicine
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: parkinson's disease no limitation ofsex, age
Exclusion criteria
Exclusion criteria: The patients who could not use the tools. The patients who did not obtain consent. The patients who have vascular disease, DM, nose disordes.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint with efficacy in PD was the change of smell test(OSIT-J) and urin 8-8OHdG from baseline to the one month.smell test and Urinary 8-OHdG were measured before treatment and after one month of intervention trial. then two months of discontinuation of the intervention was done. smell test and Urinary 8-OHdG were measured before treatment and after one month of intervention trial. | — |
Countries
Japan
Contacts
Public ContactMasaaki Hirayama
Nagoya University Graduate School of Medicine department of clinical laboratory
Outcome results
None listed