Propranolol Versus Placebo for Induction of Labor in Nulliparous Patients

Completed · Phase 2 · Has a placebo group

Conditions studied: Induction of Labor Affected Fetus / Newborn

In brief

A randomized, prospective trial will be offered to women admitted to the labor floors at Mount Sinai Medical Center for labor induction.

Key facts

Study ID

NCT03348683

Run by

Icahn School of Medicine at Mount Sinai

People needed

240

Starts

2017-12-11

Expected to finish

2018-12-11

Last updated by the study team

2020-01-07

Who can join

Age: 18 and older, up to 50. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Nulliparous women undergoing induction of labor
• >37 weeks' gestational age
• Non-anomalous, singleton cephalic presenting fetus.

You may not qualify if…

• Multiple gestations, known fetal anomalies
• Maternal cardiac or hypertensive disease
• Chronic beta blocker use
• Bronchial asthma
• Maternal or fetal indication for immediate delivery.

Where it is running

• Icahn School of Medicine at Mount Sinai — New York, New York, United States

Full record on ClinicalTrials.gov

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