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New treatment option for Placenta Accreta Spectrum
Official title Uterine Preservation in the Management of Placenta Accreta Spectrum Disorders
ClinicalTrials.gov ID: NCT06512181
What this study is testing
- What it's testing
- This study for the conservative management of placenta accreta spectrum disorders (PAS), which are a major cause of maternal morbidity and mortality. The most common management strategy for PAS in the United States is a preterm cesarean-hysterectomy.
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
- Provision of signed and dated informed consent form.
- Stated willingness to comply with all study procedures and availability for the duration of the study.
- A person with a uterus, age 18 or older
- Currently pregnant with an intrauterine gestation or postpartum
- Suspected of having PAS based on history, clinical findings, and/or imaging
You likely can't join if
- Have a low antenatal suspicion for PAS based on imaging.
See the full eligibility criteria
- Provision of signed and dated informed consent form.
- Stated willingness to comply with all study procedures and availability for the duration of the study.
- A person with a uterus, age 18 or older
- Currently pregnant with an intrauterine gestation or postpartum
- Suspected of having PAS based on history, clinical findings, and/or imaging
- Patients for whom the usual management would be peripartum hysterectomy.
- Patient desires uterine preservation or declines hysterectomy
- Agreement to adhere to Lifestyle Considerations (see section 5.3) throughout study duration.
- Have a low antenatal suspicion for PAS based on imaging.
The study team makes the final eligibility decision.
Where it's taking place
- Philadelphia, Pennsylvania, 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 Philadelphia, Pennsylvania, 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.