Adherence to Universal Aspirin Compared to Screening Indicated Aspirin for Prevention of Preeclampsia
Primary Purpose
Medication Adherence, Preeclampsia
Status
Unknown status
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Low-dose aspirin
Sponsored by
About this trial
This is an interventional prevention trial for Medication Adherence focused on measuring aspirin, preeclampsia, adherence, pregnancy
Eligibility Criteria
Inclusion Criteria:
- Pregnancy between 10 to 20 weeks gestation by best available dating
- 18 years of age or older
- Fluency in English or Spanish
Exclusion Criteria:
• Contraindication to aspirin use
Sites / Locations
- Women and Infants HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Randomized to USPSTF Criteria
Randomized to Universal aspirin receipt
Arm Description
Women randomized to knowing their risk of preeclampsia and therefore, candidates for low dose aspirin.
Women randomized to receiving low dose aspirin without knowing their risk status.
Outcomes
Primary Outcome Measures
Adherence to aspirin use
A Research Coordinator will contact each patient within 7 days of recruitment to assure the patient has picked up and has their prescription with subsequent contacts occurring at 30-day intervals until delivery.
Secondary Outcome Measures
Rates of postpartum hemorrhage
We will collect information at time of delivery of rates of postpartum hemorrhage defined as estimated blood loss of 1000 cc or greater.
Rates of preeclampsia
We will measure rates of hypertensive disease of pregnancy
Fetal growth restriction
We will measure rates of fetal growth restriction defined as estimated fetal weight or abdominal circumference <10%ile.
Placental abruption
Rates of placental abruption will be collected
Full Information
NCT ID
NCT04797949
First Posted
February 8, 2021
Last Updated
July 16, 2021
Sponsor
Women and Infants Hospital of Rhode Island
1. Study Identification
Unique Protocol Identification Number
NCT04797949
Brief Title
Adherence to Universal Aspirin Compared to Screening Indicated Aspirin for Prevention of Preeclampsia
Official Title
Adherence to Universal Aspirin Compared to Screening Indicated Aspirin for Prevention of Preeclampsia
Study Type
Interventional
2. Study Status
Record Verification Date
July 2021
Overall Recruitment Status
Unknown status
Study Start Date
March 3, 2021 (Actual)
Primary Completion Date
June 1, 2022 (Anticipated)
Study Completion Date
June 1, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Women and Infants Hospital of Rhode Island
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
There are data showing that a majority of pregnant women may not be accurately identified as high risk through screening and therefore, not receiving prophylactic low dose aspirin as recommended. This leads to missing many patients who would benefit from aspirin administration. Aspirin is an effective, affordable and safe intervention and its universal use in pregnancy has been proposed as the answer to help mitigate risk of significant morbidity from preeclampsia. However, adherence to aspirin in women at low risk compared to those deemed at high risk of preeclampsia has never been studied. One of the arguments against universal aspirin administration is the concern that universal receipt would change the compliance in those at high risk although there are no data to support this concern. To address the lack of data on differences in adherence, our goal in this proposal is to assess whether there is a difference in adherence to low dose aspirin (81 mg) in women at high risk of preeclampsia as indicated by USPSTF risk algorithm when compared to those women randomized to universal use.
Detailed Description
Research objective- To compare adherence to low dose, 81mg of aspirin in women considered high risk by USPSTF criteria vs universal receipt.
Hypothesis: Women considered high risk by USPSTF criteria will have better adherence to low dose aspirin than women randomized to universal receipt.
Study Design: Randomized trial
Population: English or Spanish speaking women between 10-20 weeks of gestation receiving their care at Women & Infants Hospital, with a plan to deliver at Women & Infants Hospital
Once enrolled, patients will then be randomized to USPSTF criteria to determine if they qualify for aspirin or to universal aspirin receipt. Once randomized, patients will undergo video pill counts at multiple intervals in their prenatal care (monthly).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Medication Adherence, Preeclampsia
Keywords
aspirin, preeclampsia, adherence, pregnancy
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Patients are randomized to receiving aspirin knowing their risk status vs those who are randomized to universal receipt.
Masking
Outcomes Assessor
Masking Description
The study personnel who will perform pill counts will be masked to the study arm.
Allocation
Randomized
Enrollment
156 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Randomized to USPSTF Criteria
Arm Type
Active Comparator
Arm Description
Women randomized to knowing their risk of preeclampsia and therefore, candidates for low dose aspirin.
Arm Title
Randomized to Universal aspirin receipt
Arm Type
Active Comparator
Arm Description
Women randomized to receiving low dose aspirin without knowing their risk status.
Intervention Type
Drug
Intervention Name(s)
Low-dose aspirin
Intervention Description
Women will be prescribed 81 mg of aspirin to take daily during pregnancy.
Primary Outcome Measure Information:
Title
Adherence to aspirin use
Description
A Research Coordinator will contact each patient within 7 days of recruitment to assure the patient has picked up and has their prescription with subsequent contacts occurring at 30-day intervals until delivery.
Time Frame
up to 42 weeks.
Secondary Outcome Measure Information:
Title
Rates of postpartum hemorrhage
Description
We will collect information at time of delivery of rates of postpartum hemorrhage defined as estimated blood loss of 1000 cc or greater.
Time Frame
These will be assessed within 24 hours after delivery.
Title
Rates of preeclampsia
Description
We will measure rates of hypertensive disease of pregnancy
Time Frame
Rates of hypertensive disease of pregnancy will be measured from 20 weeks of gestation until 6 weeks postpartum
Title
Fetal growth restriction
Description
We will measure rates of fetal growth restriction defined as estimated fetal weight or abdominal circumference <10%ile.
Time Frame
This will be measured from 24 weeks until 39 weeks.
Title
Placental abruption
Description
Rates of placental abruption will be collected
Time Frame
This will be measured from 20 weeks until 42 weeks.
10. Eligibility
Sex
Female
Gender Based
Yes
Gender Eligibility Description
Only pregnant individuals will be included regardless of gender identity.
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Pregnancy between 10 to 20 weeks gestation by best available dating
18 years of age or older
Fluency in English or Spanish
Exclusion Criteria:
• Contraindication to aspirin use
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sebastian Z Ramos, MD
Phone
401-452-0027
Email
seramos@wihri.org
First Name & Middle Initial & Last Name or Official Title & Degree
Dwight Rouse, MD
Phone
401-452-0027
Email
drouse@wihri.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sebastian Z Ramos, MD
Organizational Affiliation
Women and Infants Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Women and Infants Hospital
City
Providence
State/Province
Rhode Island
ZIP/Postal Code
02905
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sebastian Z Ramos, MD
Phone
401-452-0027
Email
seramos@wihri.org
12. IPD Sharing Statement
Citations:
PubMed Identifier
30870274
Citation
Ayala NK, Rouse DJ. A Nudge Toward Universal Aspirin for Preeclampsia Prevention. Obstet Gynecol. 2019 Apr;133(4):725-728. doi: 10.1097/AOG.0000000000003167.
Results Reference
result
PubMed Identifier
30056389
Citation
Mone F, Mulcahy C, McParland P, Breathnach F, Downey P, McCormack D, Culliton M, Stanton A, Cody F, Morrison JJ, Daly S, Higgins J, Cotter A, Hunter A, Tully EC, Dicker P, Alfirevic Z, Malone FD, McAuliffe FM. Trial of feasibility and acceptability of routine low-dose aspirin versus Early Screening Test indicated aspirin for pre-eclampsia prevention (TEST study): a multicentre randomised controlled trial. BMJ Open. 2018 Jul 28;8(7):e022056. doi: 10.1136/bmjopen-2018-022056.
Results Reference
result
PubMed Identifier
32114852
Citation
Shanmugalingam R, Wang X, Motum P, Fulcher I, Lee G, Kumar R, Hennessy A, Makris A. Clinical Influence of Nonadherence With Prophylactic Aspirin in Preventing Preeclampsia in High-Risk Pregnancies: A Multicenter, Prospective, Observational Cohort Study. Hypertension. 2020 Apr;75(4):1125-1132. doi: 10.1161/HYPERTENSIONAHA.119.14107. Epub 2020 Mar 2.
Results Reference
result
PubMed Identifier
26551178
Citation
Werner EF, Hauspurg AK, Rouse DJ. A Cost-Benefit Analysis of Low-Dose Aspirin Prophylaxis for the Prevention of Preeclampsia in the United States. Obstet Gynecol. 2015 Dec;126(6):1242-1250. doi: 10.1097/AOG.0000000000001115.
Results Reference
result
PubMed Identifier
24711050
Citation
Henderson JT, Whitlock EP, O'Connor E, Senger CA, Thompson JH, Rowland MG. Low-dose aspirin for prevention of morbidity and mortality from preeclampsia: a systematic evidence review for the U.S. Preventive Services Task Force. Ann Intern Med. 2014 May 20;160(10):695-703. doi: 10.7326/M13-2844.
Results Reference
result
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Adherence to Universal Aspirin Compared to Screening Indicated Aspirin for Prevention of Preeclampsia
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