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Effect of plant of Royan vaginal cream for the treatment of myoma with placebo

Effect of plant Royan vaginal cream for the treatment of myoma with placebo

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014042217388N1
Enrollment
90
Registered
2015-08-15
Start date
2015-08-23
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

Leiomyoma. Leiomyoma of uterus

Interventions

Intervention 1: Intervention: From the first day of menstruation, using of Royan vaginal cream full 3 applicator per night for 2 periods. Intervention 2: Control: From the first day of menstruation,
Treatment - Drugs
Intervention: From the first day of menstruation, using of Royan vaginal cream full 3 applicator per night for 2 periods.
Control: From the first day of menstruation, using of Placebo vaginal cream full 3 applicator per night for 2 periods.

Sponsors

Ardabil University of Medical Sciences.
Lead Sponsor
Bu Ali Company of Drugs Production
Collaborator

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria : All women of childbearing age (45 to 18) with at least one Fybrm to1 cm or larger, which is confirmed by ultrasound. Have a negative pregnancy test. Exclusion criteria : 1. Patients who have had hormone therapy 6 months before the treatment. 2. Patients who have had surgeries before, such as: Myomectomy. 3. Requires immediate surgical. 4. Pregnancy during the treatment 5.Abnormal Pap-Asmyr or severe anemia (8/0 )

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Reduction in bleeding volume of Myoma. Timepoint: Before and after treatment. Method of measurement: Submit in Higam table.

Secondary

MeasureTime frame
The pain of Myoma. Timepoint: Before and after intervention. Method of measurement: VAS measurement.;Size of the Myoma. Timepoint: Before and after intervention. Method of measurement: Sonography.;Life style. Timepoint: Before and after intervention. Method of measurement: Questionnaire Code SF36.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSousan Houshmandi

Ardabil University of Medical Sciences

hh4880@yahoo.com+98 45 3351 0052

Outcome results

None listed

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