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Investigation on the remission maintaining effect of Polaprezinc in patients with Crohn's disease in remission phase.

Investigation on the remission maintaining effect of Polaprezinc in patients with Crohn's disease in remission phase. - The Efficacy of Polaprezinc

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000005970
Enrollment
100
Registered
2011-07-13
Start date
2011-07-01
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

Patients with Crohn&#39

Interventions

Polaprezinc administration group: patients has Polaprezinc 150mg/day for xxx months with Crohn&#39
s disease maintenance therapy. Polaprezinc non administration group: patients treated with Crohn&#39
s disease maintenance therapy only.

Sponsors

Kawasaki Medical School
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Crohn's disease patients who have no change treatments for these three months in remission stage. Able to provide informed consent.

Exclusion criteria

Exclusion criteria: 1)Patients who had undergone total parental nutrition. 2)Patients with serious liverdysfunction and renaldysfunction 3)Patients with serious heart disease ,lung disease and hemo? 4)Patients with malignancy 5)Patients who has a allergic history against Polaprezinc 6)Patients who are pregnant or have the possibility of pregnancy 7)The patient who was judged for unsuitable by responsibility doctor.

Design outcomes

Primary

MeasureTime frame
Crohn's disease activity index at 0,1,3,6,12 months after treatment and 1 month after end point.

Secondary

MeasureTime frame
Recurrence rate Evaluation of subjective symptoms QOL(F-8) safty change of labolatory data

Countries

Japan

Outcome results

None listed

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