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The treatment using indigo naturalis for autoimmune pancreatitis

Safety of indigo naturalis in patients with autoimmune pancreatitis - Indigo naturalis for autoimmune pancreatitis

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTs051210171
Enrollment
10
Registered
2022-02-07
Start date
2022-02-26
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

Autoimmune pancreatitis Autoimmune pancreatitis

Interventions

Administration of indigo naturalis
indigo naturalis

Sponsors

Kamata Ken
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Confirmed cases of naived autoimmune pancreatitis according to the clinical diagnosis criteria 2018 (For the patients previously treated with steroid more than 180 days or more should be passed since the latest administration.) 2. Patients with abdominal symptoms 3. Patients who are 20 years old or older at the time of consent 4. Patients who can provide written consent in person.

Exclusion criteria

Exclusion criteria: 1. Patients with a history of adverse reactions or allergies to Chinese herbal medicines 2. Patients who have received other Chinese herbal medicines within 2 weeks prior to the registration date 3. Patients with a history of pulmonary arterial hypertension 4. Patients with obstructive jaundice 5. Patients with retroperitoneal fibrosis, interstitial pneumonia, or tubulointerstitial nephritis who present clinically problematic symptoms and signs 6. Patients with pseudotumor of the liver or lung 7. Patients with serious infectious diseases 8. Patients with serum creatinine level of 2.0 mg/dl or higher 9. Patients with AST or ALT levels of 50 IU/l or higher 10. Patients who are pregnant, may become pregnant, are lactating, or wish to become pregnant during the study period 11. Patients who are judged inappropriate for inclusion in this study by the physician in charge

Design outcomes

Primary

MeasureTime frame
Safety during the study

Secondary

MeasureTime frame
1. Rate of remission at 2 weeks 2. Rate of remission at 8 weeks 3. Rate of remission at 24 weeks 4. Evaluation of the AhR-IL-22 pathway

Contacts

Public ContactKen Kamata

Kindai University Hospital

ky11@leto.eonet.ne.jp+81-72-366-0221

Outcome results

None listed

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