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Conservative Management for PAS Pilot

Primary Purpose

Placenta Accreta

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Conservative management for placenta accreta spectrum (PAS)
Cesarean hysterectomy for placenta accreta spectrum (PAS)
Sponsored by
University of Utah
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Placenta Accreta focused on measuring Pregnancy

Eligibility Criteria

18 Years - 99 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 18 and older
  • History of cesarean delivery AND placenta previa OR anterior low-lying placenta AND suspected of having PAS on prenatal imaging (ultrasound/MRI)
  • Patients who would typically be recommended for hysterectomy
  • Planned delivery between 34w0d and 36w0d gestation.

Exclusion Criteria:

  • Plan to delivery before neonatal viability (<24 weeks gestation)
  • Hospitalized for antenatal hemorrhage
  • Have a low antenatal suspicion for PAS based on imaging
  • Are pregnant with multiples (twins, triplets)
  • Have a uterine fetal demise

Sites / Locations

  • University of UtahRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Conservative Management for Placenta Accreta Spectrum (PAS)

Hysterectomy at time of delivery for Placenta Accreta Spectrum (PAS)

Arm Description

Subjects who are randomized to to conservative management will undergo a cesarean delivery followed by a period of close observation in the operating room for 30-45 minutes to be sure there is no excessive bleeding or risk to keep the placenta inside

Subjects who are randomized to cesarean hysterectomy will undergo a cesarean delivery followed immediately by hysterectomy to remove the placenta and uterus together

Outcomes

Primary Outcome Measures

Number of patients completing the surgical treatment to which they are allocated
Number of patients completing the surgical treatment to which they are allocated (hysterectomy or conservative management) on the day of delivery.

Secondary Outcome Measures

Number of eligible people approached for enrollment.
Number of eligible people approached for enrollment.
Number of eligible people randomized.
Number of eligible people randomized.
Number of enrolled completing hysterectomy on day of delivery.
Number of enrolled completing hysterectomy on day of delivery.
Number of enrolled completing conservative management on day of delivery.
Number of enrolled completing conservative management on day of delivery.
Number of enrolled who don't complete their allocated treatment (drop-out).
Number of enrolled who don't complete their allocated treatment (drop-out).
Number of enrolled who are lost to follow-up through study end (inverse of retention).
Number of enrolled who are lost to follow-up through study end (inverse of retention).
Number of enrolled completing full postpartum follow-up visit schedule.
Number of enrolled completing full postpartum follow-up visit schedule.

Full Information

First Posted
October 13, 2021
Last Updated
July 6, 2023
Sponsor
University of Utah
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1. Study Identification

Unique Protocol Identification Number
NCT05139498
Brief Title
Conservative Management for PAS Pilot
Official Title
Conservative Management as an Alternative to Hysterectomy for Placenta Accreta Spectrum: a Pilot Randomized Controlled Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 26, 2022 (Actual)
Primary Completion Date
March 2026 (Anticipated)
Study Completion Date
June 30, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Utah

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Conservative in situ management is a promising alternative treatment to hysterectomy for patients with placenta accreta spectrum and may be safer and preferable for some patients. This study will assess feasibility of a future randomized clinical trial comparing these treatments and provide novel data to inform shared decision-making and cost-effective care for patients with this deadly pregnancy disorder.
Detailed Description
Placenta accreta spectrum (PAS) is an extremely morbid and increasingly common pregnancy condition that often results in massive obstetric hemorrhage. The standard treatment in the United States is hysterectomy, but this treatment is complex, morbid, and costly. A promising alternative for PAS treatment is conservative in situ management (CM), a strategy in which the placenta is left in the uterus. Unfortunately, there are insufficient data available to compare outcomes of these two treatments because past studies are limited by non-randomized study designs, minimal inclusion of patient values in making treatment decisions, and nominal consideration of economic barriers to care. A large clinical trial comparing PAS treatments is needed. But there are key logistic barriers to an adequately powered trial, including questions of whether patients will enroll and adhere to randomization allocation. This pilot trial will evaluate the feasibility of randomizing patients to CM versus hysterectomy for PAS. While pilot studies cannot make final assessments of safety and efficacy between interventions, safety and efficacy will be monitored, including those related to hemorrhage, transfusion, infection and re-operation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Placenta Accreta
Keywords
Pregnancy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
32 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Conservative Management for Placenta Accreta Spectrum (PAS)
Arm Type
Experimental
Arm Description
Subjects who are randomized to to conservative management will undergo a cesarean delivery followed by a period of close observation in the operating room for 30-45 minutes to be sure there is no excessive bleeding or risk to keep the placenta inside
Arm Title
Hysterectomy at time of delivery for Placenta Accreta Spectrum (PAS)
Arm Type
Active Comparator
Arm Description
Subjects who are randomized to cesarean hysterectomy will undergo a cesarean delivery followed immediately by hysterectomy to remove the placenta and uterus together
Intervention Type
Procedure
Intervention Name(s)
Conservative management for placenta accreta spectrum (PAS)
Intervention Description
Subjects who are randomized to to conservative management will undergo a cesarean delivery followed by a period of close observation in the operating room for 30-45 minutes to be sure there is no excessive bleeding or risk to keep the placenta inside
Intervention Type
Procedure
Intervention Name(s)
Cesarean hysterectomy for placenta accreta spectrum (PAS)
Intervention Description
Subjects who are randomized to cesarean hysterectomy will undergo a cesarean delivery followed immediately by hysterectomy to remove the placenta and uterus together
Primary Outcome Measure Information:
Title
Number of patients completing the surgical treatment to which they are allocated
Description
Number of patients completing the surgical treatment to which they are allocated (hysterectomy or conservative management) on the day of delivery.
Time Frame
Day of delivery
Secondary Outcome Measure Information:
Title
Number of eligible people approached for enrollment.
Description
Number of eligible people approached for enrollment.
Time Frame
20 weeks gestation through day of delivery
Title
Number of eligible people randomized.
Description
Number of eligible people randomized.
Time Frame
From time of consent up to one week (1-7 days) before planned delivery
Title
Number of enrolled completing hysterectomy on day of delivery.
Description
Number of enrolled completing hysterectomy on day of delivery.
Time Frame
Day of delivery
Title
Number of enrolled completing conservative management on day of delivery.
Description
Number of enrolled completing conservative management on day of delivery.
Time Frame
Day of delivery
Title
Number of enrolled who don't complete their allocated treatment (drop-out).
Description
Number of enrolled who don't complete their allocated treatment (drop-out).
Time Frame
Up to 6 weeks postpartum
Title
Number of enrolled who are lost to follow-up through study end (inverse of retention).
Description
Number of enrolled who are lost to follow-up through study end (inverse of retention).
Time Frame
Up to 6 weeks postpartum
Title
Number of enrolled completing full postpartum follow-up visit schedule.
Description
Number of enrolled completing full postpartum follow-up visit schedule.
Time Frame
Up to 6 weeks postpartum

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
Pregnant females
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18 and older History of cesarean delivery AND placenta previa OR anterior low-lying placenta AND suspected of having PAS on prenatal imaging (ultrasound/MRI) Patients who would typically be recommended for hysterectomy Planned delivery between 34w0d and 36w0d gestation. Exclusion Criteria: Plan to delivery before neonatal viability (<24 weeks gestation) Hospitalized for antenatal hemorrhage Have a low antenatal suspicion for PAS based on imaging Are pregnant with multiples (twins, triplets) Have a uterine fetal demise
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ashley Joseph
Phone
801-903-3278
Email
ashley.joseph@hsc.utah.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Marie Gibson
Phone
801-213-2845
Email
marie.gibson@hsc.utah.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Brett Einerson, MD
Organizational Affiliation
University of Utah
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Utah
City
Salt Lake City
State/Province
Utah
ZIP/Postal Code
84132
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Elizabeth Turner
Phone
801-213-2845
Email
elizabeth.e.turner@hsc.utah.edu
First Name & Middle Initial & Last Name & Degree
Brett Einerson, MD

12. IPD Sharing Statement

Plan to Share IPD
No

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