Anticholinergics for Cervical Edema in Labor
ConditionLabor Dystocia
Trial statusRecruiting
Trial phasePhase 2, Phase 3
Trial typeInterventional
Biological sexFemale
Age18+
SponsorThe University of Texas Health Science Center, Houston
About this trial
The purpose of this study is to is to determine the clinical effectiveness of a single dose of intravenous (IV) medication for the prevention of labor arrest and cesarean delivery in primiparous women undergoing trial of labor.
Eligibility criteria
Qualifiers
Primiparous
Viable single intrauterine pregnancy
Ruptured membranes
Category I tracing at time of inclusion
Disqualifiers
Category II or III tracing
Allergy to the study medication (IV Diphenhydramine)
Trial design
Treatments tested in this trial
- Treatment with Diphenhydramine
- Usual Care
Treatment groups
200 Participants
are divided into 2 treatment groupsSponsors and collaborators
Source ClinicalTrials.gov