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A Trial of Oral Misoprostol for Labor Augmentation

NCT00906347·1 site·ClinicalTrials.gov

What this study is about

Take this into the appointment.

Saves the questions and what to expect into your notes, next to the visit they belong to.

Keep this study

Lead

University of Texas Southwestern Medical Center

Age

16–any

Sex

FEMALE

Healthy volunteers

Accepted

You may be eligible if

Clinical decision to augment labor
Gestational age \> than or equal to 36 weeks
Singleton gestation
Cephalic presentation
Reassuring fetal heart rate tracing
Cervical dilation between 4 and 8 cm
Ruptured membranes with clear amniotic fluid
Intrauterine pressure catheter in place
Less than 200 MVUs in a 10 minute period
5 or fewer contractions in a 10 minute period
English or Spanish speaking patient

You may not be if

Non-reassuring fetal heart rate tracing at time of enrollment
Meconium stained amniotic fluid
Previous uterine incision
Maternal fever (defined as greater than 37.9 C)
Known fetal anomalies
Placenta previa or unexplained vaginal bleeding
Estimated fetal weight of 4,500 grams or more
Abnormal maternal bony pelvis
Grandmultiparity

The record

StatusCompleted

PhasePhase 4

Taking part350

StartedDec 2008

UpdatedNov 15, 2012

Conditions

Labor Augmentation

Where1

The University of Texas Southwestern Medical Center
Dallas, Texas, United States

Clareo Health | A Trial of Oral Misoprostol for Labor Augmentation