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Investigation of the effect of Plantago major, and Rheum on colitis

Efficacy of formula of Plantago major, and Rheum khorasanicum on clinical symptoms of patient with mild to moderate ulcerative colitis: a double blind randomized clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20150927024228N5
Enrollment
60
Registered
2023-12-18
Start date
2024-03-10
Completion date
Unknown
Last updated
2024-01-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ulcerative colitis. Ulcerative colitis

Interventions

Intervention 1: Intervention group: consumes 2 capsules daily contain two parts of Plantago major extract, and one part of Rheum khorasanicum prepared by the pharmacist in the pharmaceutical laborator

Sponsors

Kerman University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients aged 18 to 60 with mild and moderate ulcerative colitis confirmed by endoscopy and biopsy and diagnosed by a gastroenterologist who signed the informed consent form and did not meet the exclusion criteria.

Exclusion criteria

Exclusion criteria: Pregnancy or breastfeeding Taking antibiotics Taking herbal medicines, NSAIDs, OCPs or hormone therapy (in the last 2 weeks) Complications of the disease (such as massive bleeding requiring hospitalization or emergency surgery, fulminant colitis, peritonitis, toxic megacolon, obstructive stenosis), Suffering from liver, kidney, heart, cancer or celiac disease at the same time Addiction to smoking or drugs Suffering from other autoimmune diseases

Design outcomes

Primary

MeasureTime frame
Partial Mayo score. Timepoint: At the beginning of the study, 3, 6 and 10 weeks. Method of measurement: Partial Mayo score questionnaire.

Secondary

MeasureTime frame
Quality of life. Timepoint: At the beginning of the study, 3, 6 and 10 weeks. Method of measurement: Quality of life questionnaire (IBDQ-9).;Anxiety, stress, and depression. Timepoint: At the beginning of the study, 3, 6 and 10 weeks. Method of measurement: DASS-21 questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Azimi

Kerman University of Medical Sciences

Dr.azimm@gmail.com+98 34 3211 0123

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026