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Examination of the safety and the efficacy for patients using NP037 with chronic pain

Examination of the safety and the efficacy for patients using NP037 with chronic pain

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2032210400
Enrollment
50
Registered
2021-10-29
Start date
2021-11-08
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

Chronic pain

Interventions

Put on a probe of NP037 in the pain site and treatment.

Sponsors

Kondo Masako
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients aged >=20 years at the time of consent, etc.

Exclusion criteria

Exclusion criteria: Patients whom an investigator or a sub-investigator judged to have difficulty in trial enforcement, etc.

Design outcomes

Primary

MeasureTime frame
Changes in VAS from first use to the end of the first use

Contacts

Public ContactMasako Kondo

Nipro Corporation

kondo-masako@nipro.co.jp+81-77-564-0500

Outcome results

None listed

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