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Effect of Rosaceous Sinensis on primary dysmenorrhea

Evaluating the effect of Rosaceous Sinensis on the severity of dysmenorrhea in subjects with primary dysmenorrhea

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201311216807N10
Enrollment
110
Registered
2014-11-05
Start date
2014-06-16
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

Dysmenorrhea. Primary Dysmenorrhea

Interventions

Intervention 1: Control group: Water and sugar, Ten drops, Two times a day for first Three days of period. Intervention 2: Intervention group: Rosaceous Sinensis, Ten drops, Two times a day for first
Placebo
Treatment - Drugs
Control group: Water and sugar, Ten drops, Two times a day for first Three days of period
Intervention group: Rosaceous Sinensis, Ten drops, Two times a day for first Three days of period

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 24 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 18-24 years of age; regular menstrual periods with 21-35 days cycles and 3-10 days bleeding period; no identified physical and Pelvic diseases. Exclusion criteria: taking 20 drop of Rosaceous or less on two consecutive days; allergy to Rosaceous during intervention.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Intensity of pain. Timepoint: Eight weeks before treatment, Eight weeks after treatment. Method of measurement: Macgill pain scaling.

Secondary

MeasureTime frame
-. Timepoint: -. Method of measurement: -.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeddighe Amir Ali Akbari

School of Nursing and Midwifery, Shahid Beheshti University of Medical Sciences

asa_akbari@yahoo.com+98 21 8820 2512

Outcome results

None listed

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