Atomoxetine for freezing while walking
This study tests a medicine to investigate episodes when a person with Parkinson's becomes unable to step forward.
Testing a treatment or activity · Study reference: IRCT20211008052695N1
Plain-language introduction written with AI from the registry; not independently checked by a clinician. Read the original details below ↓
This registry record was last updated over six months ago, or its update date is missing. Recruitment may have changed. Confirm with the team before making plans.
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Looking for volunteers
- Start (reported date)
- 2021-09-23
Planned dates can move. A study finishing does not tell us when a paper will be published.
No results summary has been confirmed in the registry records we imported. See connected papers below; we keep checking after recruitment ends.
Changes we have recorded
- 2026-10-11 — recruiting
These are dates we observed a change, not necessarily the dates it happened.
Papers connected to this study
No connected paper has been found yet. The tracker checks the growing library for study identifiers and registry-linked publications.
Who can join?
Age range not listed · Ask the team who can join
These are starting points, not the full rules. The research team can tell you whether the study is right for your situation.
Read all the rules for taking part
Sex eligibility reported by registry: both
Full study name & original research details
Official study title
Evaluation of Atomoxetine efficacy on Freezing of gait in patient with Parkinson
Original description
Conditions reported: Parkinson disease. Secondary parkinsonism, unspecified;G21.9
Registry records for this study
Records are joined using registration identifiers. Titles alone do not establish that two studies are the same.
- IRCT · IRCT20211008052695N1 ↗ — Recruiting; WHO ICTRP processed 2021-11-29; checked 2026-10-14
- Study type
- Interventional
- Interventions
- Intervention 1: Intervention group: Group A includes 16 patients randomly selected by an uninformed person and treated with atomoxetine 40 mg for 2 weeks and then increase the dose to 80 mg for six weeks. Intervention 2: Control group: Group B includes 16 patients who are randomly selected by an uninformed person and are treated with a placebo similar to group A.
- Phases
- 3
- Sponsor
- Ahvaz University of Medical Sciences
- Start date reported by registry
- 2021-09-23 (reported)
Registry updated: Not reported · Status last verified by the registry submitter: Not reported
Registry records retrieved 2026-10-14 (UTC). Individual records may have older updates. Recruitment and eligibility must be confirmed with the study team.
Contact the research team
Public study contacts supplied to the registry. Ask whether recruitment is still open and what participation involves.
Seyed Ehsan Mohamadianinejad · +98 61 3320 4531 · D.R.ramezanirad@gmail.com
Study locations
Site status can differ from overall study status. “Status not reported” means local availability needs confirmation. Remote participation and travel arrangements must be checked with the team.
Facility not reported
Iran (Islamic Republic of)
Status not reportedThe original descriptions and participation rules come from the registry. Participation is voluntary and does not guarantee benefit.