Skip to content

Compare the effect of Tetoltoredine and solifenacin in treatment of over active bladder symptoms.

Compare the effect of extended-release toltoredine and solifenacin in the treatment of urinary frequency and nocturia in overactive bladder symptoms patients.

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016101727998N3
Enrollment
100
Registered
2017-06-10
Start date
2015-04-21
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

stress incontinance. stress incontinance

Interventions

Intervention 1: Intervention group 1: The orally sustained release drug of Tuliridin (Detrozitol ) 4 mg a day ( once a day) for two months. Intervention 2: Intervention group 2: The oral drug of
Treatment - Drugs
Intervention group 1: The orally sustained release drug of Tuliridin (Detrozitol ) 4 mg a day ( once a day) for two months.
Intervention group 2: The oral drug of ? Sulfiniacin ,4 mg a day ( once a day) for two months.

Sponsors

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

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion Criteria: Age more than 18 years; Urge incontinence; Mixed incontinence; urination in the day more than 8 times and urination in the night more than once; more than once a day with urge incontinence; Sense of urgency to urinate in 24 hours. Exclusion Criteria: Lack of consent to the participation; Contraindications received antimuscarinic drugs such as glaucoma.

Exclusion criteria

Exclusion criteria:

Design outcomes

Secondary

MeasureTime frame
Drug complication. Timepoint: two month after treatment. Method of measurement: Ask the patient.

Primary

MeasureTime frame
Urinary frequency. Timepoint: Before and two month after treatment. Method of measurement: Specific Questionaire.;Nuctury ( frequency of night urination ). Timepoint: Before and two month after treatment. Method of measurement: Specific Questionaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr.Maryam Hajhashemy

Pelvic Clinic of Valiasr Hospital

hajhashemy73@yahoo.com+98 21 6119 2363

Outcome results

None listed

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