NCT00432588

Brief Summary

Hypothesis (H0): Labor duration and obstetric complications are not significantly different in the three groups (misoprostol-dinoprostone-oxytocin).

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 6, 2007

Completed
2 days until next milestone

First Posted

Study publicly available on registry

February 8, 2007

Completed
Last Updated

June 1, 2007

Status Verified

February 1, 2007

First QC Date

February 6, 2007

Last Update Submit

May 31, 2007

Conditions

Keywords

IUFDPOSTTERMROM

Interventions

Eligibility Criteria

Sexfemale
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Term pregnancy
  • Singleton
  • Vertex
  • Bishop score below 6

You may not qualify if:

  • History of drug reaction
  • Medical disease
  • IUGR
  • Oligohydramnios
  • Vaginal bleeding
  • Fetal anomaly
  • Uterine scar

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Shariaty Maternity Hospital

Tehran, Iran

Location

Related Links

MeSH Terms

Conditions

Pre-EclampsiaFetal DeathFetal Membranes, Premature Rupture

Interventions

MisoprostolDinoprostone

Condition Hierarchy (Ancestors)

Hypertension, Pregnancy-InducedPregnancy ComplicationsFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesDeathPathologic ProcessesPathological Conditions, Signs and SymptomsObstetric Labor Complications

Intervention Hierarchy (Ancestors)

Prostaglandins E, SyntheticProstaglandins, SyntheticProstaglandinsEicosanoidsFatty Acids, UnsaturatedFatty AcidsLipidsAutacoidsInflammation MediatorsBiological FactorsProstaglandins E

Study Officials

  • Mitra Ahmad Soltani

    Hormozgan University of Medical Sciences

    PRINCIPAL INVESTIGATOR
  • Minoo Rajaee Lari, Perinatologist - Obs and Gyn

    Department of Obs and Gyn - HUMS

    STUDY CHAIR

Study Design

Study Type
interventional
Phase
phase 1
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER

Study Record Dates

First Submitted

February 6, 2007

First Posted

February 8, 2007

Last Updated

June 1, 2007

Record last verified: 2007-02

Locations