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The effect of evening primrose in the treatment of missed abortion process.

A comparative study on the effect of vaginal misoprostol usage with the combination of evening primrose and vaginal misoprostol in the treatment of missed abortion.

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20160308026971N8
Enrollment
140
Registered
2020-02-15
Start date
2019-11-12
Completion date
Unknown
Last updated
2020-02-24

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

Conditions

Missed abortion. Missed abortion

Interventions

Intervention 1: Intervention group: In addition to routine treatment of missed abortion with vaginal misoprostol, Two 1000 mg primerose capsules made by Barij essential company,10 pm before hospitali

Sponsors

Rafsanjan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: All of women with a diagnosis of missed abortion Inclination to participate in the study Selection of Niknafs hospital for abortion induction

Exclusion criteria

Exclusion criteria: Vaginal bleeding diseases associated with disorders Hemorrhagic agents, anticoagulant drugs, Patients with history of psychiatric disorders in the phenothiazine category, and epilepsy patients

Design outcomes

Primary

MeasureTime frame
Dosage of misoprostol. Timepoint: After the abortion is complete. Method of measurement: Information recorded in the file.;Disposal time of pregnancy products. Timepoint: After the abortion is complete. Method of measurement: Information recorded in the file.;The severity of the bleeding. Timepoint: After the abortion is complete. Method of measurement: Information recorded in the file.

Secondary

MeasureTime frame
Pain rate. Timepoint: During of the hospitalization. Method of measurement: Visual analogue scale.;Number of days of hospitalization. Timepoint: After the patient is discharged. Method of measurement: The information recorded in the file.;Curettage. Timepoint: During of the hospitalization. Method of measurement: The information recorded in the file.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMarzeyeh Loripoor

Rafsanjan University of Medical Sciences

marzeyehloripoor@yahoo.com+98 34 3428 0035

Outcome results

None listed

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