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Safety of dietary supplements including n-3 PUFA (Imark S®) for the maintenance of remission in patients with Crohn's disease: A pilot study.

Safety of dietary supplements including n-3 PUFA (Imark S®) for the maintenance of remission in patients with Crohn's disease: A pilot study. - Safety of dietary supplements including n-3 PUFA for CD.

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000012585
Enrollment
5
Registered
2014-01-10
Start date
2014-01-10
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

Crohn&#39

Interventions

After 3 month intervention with Imark S supplements, to compare the data before ingestion with after each months intervention. 1 month(30 days): 1 bottle of ingestion/ a day 2 month(30 days): No ing

Sponsors

Osaka University Graduate School Department of Complementary and Alternative Medicine
Lead Sponsor
Osaka University Graduate School Department of Gastroenterology
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients diagnosed with Crohn's diseases. 2) Patients expected over 3 month-survival from the first day of this study. 3) Patients who can orally ingestion. 4) Patients whose condition are in remission 5) Patients who are obtained with the prior written consent.

Exclusion criteria

Exclusion criteria: 1) Patients with the following diseases. (cirrhosis, chronic renal failure, diabetes with insulin therapy and so on) 2) Patients with steroid treatment 3) Patients with anti-TNF agents treatment 4) Patients with food allergy 5) Patients less than 20 years old. 6) Patients with xerosis cutis and impossible to measure body composition 7) Patients judged to be inappropriate for this study from the doctor in charge.

Design outcomes

Primary

MeasureTime frame
Safety study (Blood test indicators, inflammatory cytokine, CDAI)

Secondary

MeasureTime frame
Safety check depending on the number of intake.(100ml X 1 or 2 bottle) Efficacy check of maintenance for remission.(Using CDAI score)

Countries

Japan

Contacts

Public ContactAsuka Yasueda

Osaka University Graduate School of Medicine Department of Complementary and Alternative Medicine

a-yasueda@cam.med.osaka-u.ac.jp06-6879-3498

Outcome results

None listed

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