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Efficacy of Isosorbide dinitrate in cervical ripening

A comparision of out patient oral and vaginal Isosorbide dinitrate in cervical ripening befor induction of labor in post term pregnancy with low bishop score

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201108157334N1
Enrollment
150
Registered
2012-10-08
Start date
2012-03-19
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Isosorbide dinitrate effect on cervical ripening. Disorders related to long gestation and high birth weight

Interventions

Intervention 1: Samples of investigation are divided into three groups based on randomly numbers table., in one group isosorbide dinitrate 40 mg should be placed vaginaly in posterior fornix.The Bis
Treatment - Drugs
Samples of investigation are divided into three groups based on randomly numbers table., in one group isosorbide dinitrate 40 mg should be placed vaginaly in posterior fornix.The Bishop score is det
Samples of investigation are divided into three groups based on randomly numbers table., in one group isosorbide dinitrate20 mg should be given oraly.The Bishop score is determined at the beginning of
Samples of investigation are divided into three groups based on randomly numbers tablethat one group is control.they dont take any drug.The Bishop score is determined at the beginning of the study.THE

Sponsors

Vice chancellor for research of Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
10 Years to 50 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1)Nulliparity 2)Gestational age>42 weeks 3)Bishop score<5 4)Singleton pregnancy 5)Cephalic presentation 6) filled Consent form. Exclusion criteria: 1)Premature rupture of membrane 2)Vaginal bleeding 3)Contraindication for ISDN 4)History of any uterian scar 5)Intolerance to ISDN 6)Any systemic disease 7)Laber pain 8)Oligohydramnios 9)IUGR 10)Non-reassuring FHR

Exclusion criteria

Exclusion criteria:

Design outcomes

Secondary

MeasureTime frame
Time from full dilatation to delivery. Timepoint: Stage 2 of labor. Method of measurement: Minut.;Time from active phase to full dilation. Timepoint: Stage 1 of labor. Method of measurement: Minut.;From induction to active phase. Timepoint: active phase. Method of measurement: minut.

Primary

MeasureTime frame
Cervical ripening. Timepoint: 24 hours. Method of measurement: Vaginal exam.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Ladan Haghighi

Tehran University of Medical Sciences

l-haghighi@sina.tums.ac.ir+98 21 66111

Outcome results

None listed

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