Evaluation of Clinical Effects for the Treatment of Cervical Dystonia Using Devices Induce the Hanger Reflex

Evaluation of Clinical Effects for the Treatment of Cervical Dystonia Using Devices Induce the Hanger Reflex - Effects for Cervical Dystonia Using Devices Induce the Hanger Reflex

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000021301

Enrollment

Registered

2016-03-02

Start date

2015-07-28

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

Cervical Dystonia

Interventions

Toronto Western Spasmodic Torticollis Rating Scale

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: (1)Patients diagnosed as cervical dystonia, and having restrection of head rotation. (3)Patients can visit hospital.

Exclusion criteria

Exclusion criteria: (1)Patients who don't have hanger reflex (2)Patients having a unstable disease, and possibility to change medicines during study (3)Patient ruled unfit by a doctor responsible for the study.

Design outcomes

Primary

Measure	Time frame
Evaluate changes between Toronto Western Spasmodic Torticollis Rating Scale (TWSTRS) scores before and 3 months after the trial	—

Countries

Japan

Contacts

Public ContactYukio Mukai

Administrative department Administration section

kn-spd@med.email.ne.jp076-246-5600

Outcome results

None listed

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