Skip to content

Efficacy of Luvos®Healing Earth supplementation to mebeverine in Irritable Bowel Syndrom relief

Efficacy of adding Luvos®Healing Earth supplementation to mebeverine in symptom and quality of life relief in patients with diarrhea dominant Irritable Bowel Syndrome

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20141201020178N7
Enrollment
70
Registered
2018-03-01
Start date
2017-01-21
Completion date
Unknown
Last updated
2018-03-26

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

Conditions

Irritable bowel syndrome diarrhea dominant. Irritable bowel syndrome with diarrhea

Interventions

Intervention 1: Intervention Group: Mebeverine Tablet, 135 milligram twice a day in combination with 1 sachet of Luvos®Healing Earth twice a day . Intervention 2: Control group: Mebeverine Tablet, 135

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: All patients with diarrhea dominant irritable bowel syndrome based on Rome's criteria 4(at least 1 time per week abdominal pain related to defication and 2 of the other criteria at least in 1/4 of defication :stool frequency>3 /day,abnormal loose stool form ,defecatory urgency, mucus with bowel movements) age beween 18-65 years old

Exclusion criteria

Exclusion criteria: Lactase deficiency Celiac disease Inflammatory bowel disease Food allergy Peregnancy Systemic disease(Diabetes Melitous,Hypertention, Cardiac ,Pulmonary ,Renal,liver,Thyroid disease, Cancer,Myopathy, Neuropathy, Sclerodermia) History of abdominal surgery History of allergy to periscribed medication Non-compliant and uncooperative

Design outcomes

Primary

MeasureTime frame
Quality of life in patients with Irritable Bowel syndrome diarrhea dominant. Timepoint: before intervention and 2, 4 weeks after intervention. Method of measurement: Quality of Life questionnaire.;Symptoms in patients with Irritable Bowel syndrome diarrhea dominant. Timepoint: before intervention and 2, 4 , 6 weeks after intervention. Method of measurement: Symptom severity score.

Secondary

MeasureTime frame
Patient compliance rate. Timepoint: 2 and 4 weeks after intervention. Method of measurement: Data gathering sheet.;Adverse effect rate. Timepoint: 2 and 4 weeks after intervention. Method of measurement: Data gathering sheet.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMarjan Mokhtare

Iran University of Medical Sciences

marjanmokhtare@yahoo.com+98 21 6655 4790

Outcome results

None listed

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