Clinical research for relationship between serum IL-31 and pruritus in patients who undergo hemodialysis

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-jRCT1080224513

Enrollment

100

Registered

2019-01-11

Start date

2018-10-30

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

hemodialysis

Interventions

investigational material(s) Generic name etc : - INN of investigational material : - Therapeutic category code : --- Other Dosage and Administration for Investigational material : - control material(

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: - Personally provided written informed consent for the clinical study and able to comply with the requirements of the study protocol - Aged =>20 and <75 years old at the time of informed consent - Has undergone hemodialysis (including hemodiafiltration) 3 times a week for at least 12 weeks before enrollment

Exclusion criteria

Exclusion criteria: - Deemed unsuitable as a subject in the study by the investigator for some other reason

Design outcomes

Primary

Measure	Time frame
exploratory -	—

Secondary

Measure	Time frame
exploratory -	—

Countries

Japan

Outcome results

None listed

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