Efficacy of biological dressing (amniodisk) in preventing disease progression of cervical intraepithelial neoplasia, grade 1 (CIN1)

Assessment the efficacy of biological dressing (amniodisk) in preventing disease progression in women with cervical intraepithelial neoplasia, grade 1 (CIN1)

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20151020024625N21

Enrollment

Registered

2024-10-12

Start date

2024-11-05

Completion date

Unknown

Last updated

2025-01-08

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

Conditions

Cervical intraepithelial neoplasia , grade 1. Mild cervical dysplasia

Interventions

Intervention 1: Intervention group: After the initial biopsy and pathology test and confirmation of the diagnosis, a biological dressing (amniotic membrane) is placed on the cervix and to help its abs

Eligibility

Sex/Gender

Female

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients with cervical intraepithelial neoplasia, grade 1(CIN1)

Exclusion criteria

Exclusion criteria: Having any infectious process Patients wuth diabetes, renal and liver disorders Having any type of malignancy

Design outcomes

Primary

Measure	Time frame
Progression or remission of the disease. Timepoint: Six months after ntervention. Method of measurement: Biopsy and pathology method.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactElham Saffarieh

Semnan University of Medical Sciences

eli_saffarieh@yahoo.com+98 23 3346 0055

Outcome results

None listed

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