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Comparative study of efficacy and complications of two cervical preparations in term and preterm pregnancies

Comparative study of efficacy and complications of two cervical preparations in term and preterm pregnancies

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20130812014333N137
Enrollment
50
Registered
2020-02-05
Start date
2020-01-15
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

Pregnancy. Encounter for supervision of normal pregnancy

Interventions

Intervention 1: In the first intervention group, oxytocin will be injected simultaneously with the balloon inserted at the appropriate position. Injections will be started at 2 mu/min oxytocin and con

Sponsors

Kermanshah University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: Mother age between 18-35 years Lack of medical diseases such as diabetes, heart disease, pulmonary, renal disease, hypertension and history of hospitalization due to mental illness Body mass index less than 26

Exclusion criteria

Exclusion criteria: Indication for termination of pregnancy Use oxytocin before and during the first contraction monitor Cesarean section for some reason except stopping delivery or pelvic stenosis

Design outcomes

Primary

MeasureTime frame
Postpartum hemorrhage. Timepoint: After the end of the study. Method of measurement: Based on patient records.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Fatahi

Kermanshah University of Medical Sciences

rezaei120alireza@yahoo.com+98 83 3427 6306

Outcome results

None listed

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