Studying the effect of Ramesh vaginal suppositories on mixed infections in women of reproductive age

Studying the effect of Ramesh vaginal suppositories on mixed leucorrhea in women of reproductive age

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20241231064231N1

Enrollment

Registered

2025-03-15

Start date

2025-01-20

Completion date

Unknown

Last updated

2025-07-21

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

Conditions

Mixed lokura.

Interventions

Intervention 1: Intervention group: Will take Ramesh suppositories in addition to the experimental treatment of common vaginitis (combination of metronidazole and clotrimazole). Intervention 2: Contro

Eligibility

Sex/Gender

Female

Age

18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Women aged 18-49 Married Literate Non-pregnant With at least one failed conventional treatment

Exclusion criteria

Exclusion criteria: History of drug sensitivity to common treatment for mixed infection

Design outcomes

Primary

Measure	Time frame
Volume and color of the leucorrhea. Timepoint: Weeks 4, 8 and 12. Method of measurement: Vaginal examination.	—

Secondary

Measure	Time frame
Vaginal burning and itching. Timepoint: Weeks 4, 8 and 12. Method of measurement: Clinical examination and interview.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAzam Rahmani

Tehran University of Medical Sciences

azamrahmani7@gmail.com+98 21 6105 4566

Outcome results

None listed

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