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New treatment option for Pregnancy
Official title Optimizing Timing of Cesarean Delivery Consent on Labor and Delivery
ClinicalTrials.gov ID: NCT07117708
What this study is testing
- What it's testing
- Nationally, 32.1% of pregnant patients deliver via cesarean delivery, including both patients who undergo a planned cesarean delivery and patients who intend to undergo vaginal delivery and are recommended to deliver via cesarean delivery. The investigators aim to understand how to optimize the patient experience for patients who present to the hospital intending to deliver vaginally but are recommended to deliver via cesarean delivery (an unplanned cesarean delivery).
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older, women only
You may be able to join if
- 18 years of age or older
- Receiving prenatal care at Duke Perinatal Durham or Duke Women's Health Associates
- Between 34 weeks 0 days and 41 weeks 0 days of gestation
- Scheduled for induction of labor OR are eligible/intend to be scheduled for an induction of labor
You likely can't join if
- Trial of labor after cesarean delivery
- Multiple gestation
- Major fetal anomalies
- Presenting for induction of labor as a transfer from the antepartum inpatient service
- Non-English speaking
- Those who do not intend to labor
See the full eligibility criteria
- 18 years of age or older
- Receiving prenatal care at Duke Perinatal Durham or Duke Women's Health Associates
- Between 34 weeks 0 days and 41 weeks 0 days of gestation
- Scheduled for induction of labor OR are eligible/intend to be scheduled for an induction of labor
- Trial of labor after cesarean delivery
- Multiple gestation
- Major fetal anomalies
- Presenting for induction of labor as a transfer from the antepartum inpatient service
- Non-English speaking
- Those who do not intend to labor
- Patients who are ineligible for vaginal delivery for other reasons, including fetal malpresentation or abnormal placentation
The study team makes the final eligibility decision.
Where it's taking place
- Durham, North Carolina, United States
Compensation & support
Compensation mentioned.
ClinicalTrials.gov doesn't provide a reliable structured field for payment or travel support - confirm details with the study team.
Questions & answers
Do participants get paid in this trial?
This study's listing includes signals that participants may be compensated or receive a stipend. Amounts vary and are set by the study team - confirm the details with them.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling female, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Durham, North Carolina, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.