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The effectivness of Dracocephalum Kotschyi on irritable bowel syndrome (IBS)

Irritable bowel syndrome Explanation based on Iranian Tradition Medicine and The effectivness of Dracocephalum Kotschyi on quality of life and IBS Severity in patient (18-50 years old) with diarrhea-predominant or mixed type irritable bowel syndrome

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180823040854N1
Enrollment
76
Registered
2019-07-30
Start date
2018-04-07
Completion date
Unknown
Last updated
2019-10-07

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 1: Intervention group :Hydro alcohol extract capsule of Dracocephalum Kotschyi manufactured in the School of Pharmacy of Isfahan University of Medical Sciences, three times a day each ti

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Definite diagnosis of irritable bowel syndrome based on Rome 3 criteria and confirmation of diagnosis by a gastrointestinal specialist Patients with irritable bowel syndrome of diarrhea type or a mixed type Patients with moderate severityof irritable bowel syndrome Within the age group of 18-50 years Not being afflicted with psychiatric disorders Informed consent for study Having a normal colonoscopy and para-clinic evidences of intestinal cancer and other related differential diagnosis Not taking any other drug in order to treat IBS disorder

Exclusion criteria

Exclusion criteria: Be pregnant from the beginning History of severe sensitivity reactions to aromatic substances

Design outcomes

Primary

MeasureTime frame
Life quality of patients afflicted with irritable bowel syndrome and its areas. Timepoint: -In the beginning of the study (before the intervention begins) and one month after the beginning of taking Dracocephalum Kotschyi and one month after cutting its consumption. Method of measurement: The questionnaire of life quality of patients afflicted with irritable bowel syndrome.;Severity in patient of Irritable bowel syndrome. Timepoint: -Determination of severity of irritable bowel syndrome symptoms in the beginning of the study (before the intervention begins) and one month after the beginning of taking Dracocephalum Kotschyi and one month after cutting its consumption. Method of measurement: -The questionnaire and index of severity of irritable bowel syndrome symptoms.

Secondary

MeasureTime frame
Life quality mark in those afflicted with irritable bowel syndrome. Timepoint: In the beginning of the study (before the intervention begins) and one month after the beginning of taking Dracocephalum Kotschyi and one month after cutting its consumption. Method of measurement: The quality of life in those afflicted with irritable bowel syndrome.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParisa Heydari

Esfahan University of Medical Sciences

parisaa_sooresh@yahoo.com+98 31 3668 8138

Outcome results

None listed

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