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Compares treatment options for Placenta Previa
Official title Planned Delivery at 37 Versus 36 Weeks in Pregnancies With Placenta Previaand Accreta
ClinicalTrials.gov ID: NCT07025954
What this study is testing
- What it's testing
- Current clinical practice guidelines recommend planned cesarean delivery(CD) at 34-37 weeks of gestation in pregnant women with placenta previa and accreta. Preterm birth may lead to neonatal immaturity, while laterCD may increase the risk of severe hemorrhage and surgery complications.
- 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 to 45, women only
You may be able to join if
- 28-34 weeks of gestation.
- Both ultrasound and MRI indicate placenta previa with placenta accreta spectrum (PAS).
- Planned to undergo cesarean delivery at the participating study hospitals.
- Agree to participate and sign the informed consent form.
You likely can't join if
- Multiple gestation.
- Other obstetric complications (e.g., preeclampsia, vasa previa), and severe maternal medical conditions (e.g., uncontrolled diabetes, progressive...
- Major uterine structural anomalies (e.g., uterine didelphys, Uterine tumors ≥5 cm).
- Estimated fetal weight \<3rd percentile for gestational age, major congenital anomalies, intrauterine fetal demise.
The study team makes the final eligibility decision.
Where it's taking place
- Guangzhou, Guangdong, China
- Zhengzhou, Henan, China
- Chengdu, Sichuan, China
- Beijing, China
- Chongqing, China
- Guangzhou, China
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 to 45 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Guangzhou, Guangdong, China; Zhengzhou, Henan, China; Chengdu, Sichuan, China; Beijing, China; Chongqing, China; Guangzhou, China. 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.