Impact of Medjool Date Consumption on Labor and Delivery Outcomes
Recruiting
N/A
Interventional Study
Spontaneous Labor
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Interventional
- Purpose
- Other
- Participants needed
- 250 (estimated)
- Sponsor
- The Cleveland Clinic · Other
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About This Trial
The proposed Medjool date randomized trial will help inform clinical practice regarding the utility of Medjool date consumption for labor onset by comparing the incidence of spontaneous labor with the need for labor induction in patients who have been randomized to consume Medjool dates from 34 weeks gestation through the day after delivery day. The study will secondarily investigate the relations…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Singleton pregnancy less than 36weeks 0 days gestational age
* Age ≥18 years old
* Has decision-making capacity and able to provide informed consent for research participation
* Able to speak, read and understand English
* Planned delivery at a Cleveland Clinic Institution
Ex…
Contacts