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Efficacy of Traditional Iranian Medicine Product in Control of Urinary Incontinence in Women

The Comparison Between Traditional Iranian Medicine Product Consist of "Myrtus Communis" with "Toltrodine" in Control of Urge Urinary Incontinence in Women

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014102819734N1
Enrollment
72
Registered
2015-01-13
Start date
2013-08-23
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

urge urinary incontinence. Other specified urinary incontinence

Interventions

Intervention 1: Intervention group: Traditional Herbal Syrup which is a aqueous extract of "Myrtus Communis" leaves. Dosage: 15 cc 20-40 min after each meal means 45 cc per day. Intervention 2: Contro
Treatment - Drugs
Intervention group: Traditional Herbal Syrup which is a aqueous extract of "Myrtus Communis" leaves. Dosage: 15 cc 20-40 min after each meal means 45 cc per day.
Control group: Tab 2 mg "Toltrodine" 2 times a day.

Sponsors

Vice Chancellor for Research, Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Female with urge incontinence or mixed incontinence with urge dominance; Who have been symptomatic from at least 3 months ago; Not have been treated for at least 2 week; and are health mentally. Exclusion criteria: Positive urine culture; Uncontrolled diabetic; Uncontrolled HTN; History of glaucoma; History of drug allergy; Neuralgic disease; Bladder cancer; Hematuria; Residual volume more than 110 in sonography; Any voiding dysfunction in history

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Reduction of the symptoms severity. Timepoint: Before and 4 weeks after treatment. Method of measurement: ICIQ-SF questionnaire.

Secondary

MeasureTime frame
Advers effect of drug. Timepoint: any time after starting drug. Method of measurement: asking from patients.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Nojavan

Research Institute for Islamic and Complementary Medicine

nojavan.f@tak.iums.ac.ir+98 21 3316 8839

Outcome results

None listed

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