Uterine Preservation in the Management of Placenta Accreta Spectrum Disorders

Not Applicable

Not yet recruiting

• Conditions: Placenta Accreta Spectrum

• Registration Number: NCT06512181
• Lead Sponsor: University of Pennsylvania

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2024-7-16
• Last Update Posted: 2 September 2024

Recruitment & Eligibility

• Status: Not yet recruiting
• Sex: Female
• Target Recruitment: Not specified

Inclusion Criteria

Inclusion Criteria:<br><br> 1. Provision of signed and dated informed consent form.<br><br> 2. Stated willingness to comply with all study procedures and availability for the<br> duration of the study.<br><br> 3. A person with a uterus, age 18 or older<br><br> 4. Currently 16-36 weeks pregnant with an intrauterine gestation<br><br> 5. History of cesarean delivery AND placenta previa OR anterior low-lying placenta AND<br> suspected of having PAS on prenatal imaging (ultrasound/MRI)<br><br> 6. Patients for whom the usual management would be cesarean-hysterectomy.<br><br> 7. Patient desires uterine preservation<br><br> 8. Agreement to adhere to Lifestyle Considerations (see section 5.3) throughout study<br> duration.<br><br>Exclusion Criteria:<br><br>• Have a low antenatal suspicion for PAS based on imaging.

Exclusion Criteria

Not provided

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Hysterectomy rate

Secondary Outcome Measures

Name	Time	Method
Endometritis rate;Coagulopathy rate;Frequency of vaginal bleeding;Frequency of pelvic pain