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Comparison of the effect of combined mechanical-pharmacological method with pharmaceutical method on preparation of cervix and induction of labor in pregnant women

Comparison of the effect of combined mechanical-pharmacological method with pharmaceutical method on preparation of cervix and induction of labor in pregnant women with gestational age of =37 weeks and cervix length =20 mm

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240816062778N1
Enrollment
106
Registered
2024-09-01
Start date
2024-09-22
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

Childbirth. Pre-existing essential hypertension complicating pregnancy, childbirth and the puerperium

Interventions

Intervention 1: In the misoprostol group, the drug is placed vaginally with a dose of 25 micrograms in the posterior fornix after the initial examination. If there is no change in dilatation, misopros

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Pregnant women aged 18-45 gestational age of =37 weeks cervix length =20 mm

Exclusion criteria

Exclusion criteria: Pregnant women >45 years Pregnant women <18 years

Design outcomes

Primary

MeasureTime frame
The duration of the active phase of labor. Timepoint: Upon admission and then 6 hours later and then every 2 hours. Method of measurement: In both study groups, examinations are performed by two obstetrics and gynecology assistants. Patients will undergo a vaginal examination upon admission and then 6 hours later and every 2 hours thereafter.;The time interval from the start of induction to entering the active labor phase. Timepoint: Upon admission and then 6 hours later and then every 2 hours. Method of measurement: In both study groups, examinations are performed by two obstetrics and gynecology assistants. Patients will undergo a vaginal examination upon admission and then 6 hours later and every 2 hours thereafter.;Duration of hospitalization until delivery. Timepoint: Upon admission and then 6 hours later and then every 2 hours. Method of measurement: In both study groups, examinations are performed by two obstetrics and gynecology assistants. Patients will undergo a vaginal examination upon admission and then 6 hours later and every 2 hours thereafter.;Duration of bleeding. Timepoint: Upon admission and then 6 hours later and then every 2 hours. Method of measurement: In both study groups, examinations are performed by two obstetrics and gynecology assistants. Patients will undergo a vaginal examination upon admission and then 6 hours later and every 2 hours thereafter.;Severity of bleeding. Timepoint: Upon admission and then 6 hours later and then every 2 hours. Method of measurement: In both study groups, examinations are performed by two obstetrics and gynecology assistants. Patients will undergo a vaginal examination upon admission and then 6 hours later and every 2 hours thereafter.;The duration of the initiation of the induction method until delivery. Timepoint: Upon admission and then 6 hours later and then every 2 hours. Method of measurement: In both study groups, examinations are performed by two obstetrics and gynecology assistants. Patients will un

Countries

Iran (Islamic Republic of)

Contacts

Public ContactElaheh Sadati

Shahid Beheshti University of Medical Sciences

seyedehelahesadati@gmail.com+98 21 2243 9872

Outcome results

None listed

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