FindTrial
Sign In

HyLink Customer Survey

HyLink Customer Survey - HyLink Customer Survey

Status
Active, not recruiting
Phases
Unknown
Study type
Unknown
Source
JPRN
Registry ID
JPRN-UMIN000044270
Enrollment
200
Registered
2021-05-28
Start date
2021-06-01
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

Osteoarthritis of the Knee

Interventions

None listed

Sponsors

SEIKAGAKU CORPORATION
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Nothing.

Exclusion criteria

Exclusion criteria: 1. Subjects for whom the product is contraindicated according to the Instructions For Use or subjects to whom, in any case, the product is administered not in accordance with the Instructions For Use. 2. Subjects with a history of hypersensitivity due to any ingredients of HyLink.

Design outcomes

Primary

MeasureTime frame
Safety - Occurrence of adverse events and adverse reactions—

Secondary

MeasureTime frame
Efficacy - Changes from baseline of pain in osteoarthritis (OA) of the knee—

Countries

Europe

Contacts

Public ContactTadamasa Kobayashi

SEIKAGAKU CORPORATION Pharmacovigilance Dept.

ce_pms@seikagaku.co.jp0352208556

Outcome results

None listed

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