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Effect of the combination of Achillea millefolium, Shirazi Matricaria chamomilla and Glycyrrhiza glabra on irritable bowel syndrome

Critical Trial of the effect of the combination of Achillea millefolium, Shirazi Matricaria chamomilla and Glycyrrhiza glabra on irritable bowel syndrome symptoms

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013093014827N1
Enrollment
102
Registered
2013-11-19
Start date
2013-09-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Irritable bowel syndrome. Irritable bowel syndrome

Interventions

Intervention group: intervention group receives one 100 mg tablet per 8 hours which is the combination of three plants
Intervention 1: Intervention group: intervention group receives one 100 mg tablet per 8 hours which is the combination of three plants
Achillea millefolium, Shirazi Matricaria chamomilla and Glycyrrhiza glabra ( The tablets are produced by Goldaru Company and are available in the market ). The intervention period duration is 15 days.
Treatment - Drugs
Control group: control group receives placebo 100 mg tablets that are like drug tablets for every 8 hours which is without effective material. The placebo is made by pharmacologist of the Tohid Medica

Sponsors

Vice Chancellor for research of Kurdistan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 90 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Patients with irritable bowel syndrome diagnostic according to ROM III Criteria; Age 15-90 years; living in Sananadaj Exclusion Criteria: Patients who had undergone abdominal surgery or other abdominal diseases; patients who are not willing to discontinue current medications; medical complications; coagulation problems

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Abdominal Pain. Timepoint: Beginning of the study, 2weeks later, Four weeks later. Method of measurement: Mild , Moderate, Sever.

Secondary

MeasureTime frame
Change in excretion pattern. Timepoint: Zero, 2 weeks after intervention, four weeks after initiation of treatment. Method of measurement: clinical history as constipation, diarrhea and normal.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactKhaled Minooi

Faculty of Medicine,Kurdistan university of Medical Sciences

kminooi@yahoo.com+98 87 1613 1301

Outcome results

None listed

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