Postpartum Low-Dose Aspirin After Preeclampsia for Optimization of Cardiovascular Risk (PAPVASC)
Trial Snapshot
- Phase
- Early Phase 1
- Status
- Terminated
- Sponsor
- Enrollment
- 14
- Locations
- 1
- Primary Endpoint
- Endothelium-Dependent Dilation
Study Overview
Brief Summary
Women who develop preeclampsia (PE) in pregnancy are at a greater risk for adverse cardiovascular health outcomes. PE is associated with vascular remodeling and functional changes in the postpartum, reflective of its systemic effects during gestation. Aberrant microvascular endothelial function has been demonstrated in pharmacological studies of formerly preeclamptic women. However, clinicians do not have any recourse for modulating vascular functional adaptations nor mitigating the future risk for maternal disease in the early postpartum. Low-dose aspirin (LD-ASA) is commonly prescribed to prevent PE and confers a consistently positive effect on mitigating PE risk when given in early gestation to women at risk. While the precise effect of LD-ASA on PE development is not fully understood, existing evidence suggests it may confer an array of anti-thrombotic, vasodilatory, pro-endothelial effects that mitigate the risk of disease.
This study will be a randomized, placebo-controlled trial of LD-ASA administration over 6 months in the early postpartum in women with prior severe PE. Women will be identified, enrolled, and randomized to either treatment or placebo groups. Treatment groups will receive 81 mg daily oral aspirin, while control groups will receive an equivalent placebo pill. Vascular functional assessment at study outset will take place, combining laser speckle contrast imaging and iontophoresis of dilute vasoactive drug solutions. Blood and urine will be obtained for analysis of cardiometabolic and endothelial factors. Participants will take their assigned study drug for 6 months, after which a retest appointment will take place to assess vascular functional changes.
Detailed Description
This study will be a prospective, randomized, controlled, double-blinded, single-centre trial with two parallel groups. The primary outcome will be endothelium-dependent vasodilation as measured by iontophoresis and laser speckle contrast imaging (LSCI).
Participants will be recruited following a preeclamptic delivery at Kingston Health Sciences Center. Following confirmation of eligibility, they will be randomized to treatment or control groups. Randomization will be performed as block randomization with a 1:1 allocation ratio. In total, 44 participants will be recruited and randomized, with 22 being assigned to each treatment arm.
Prior to discharge from the hospital, investigators will assess both vascular functional and biochemical variables in each participant. Using LSCI, a non-invasive imaging modality, investigators will continuously measure microvascular blood flow in the volar forearm in response to dilute drug solutions administered using iontophoresis. Iontophoresis refers to the non-invasive administration of drugs under the influence of an applied current. Iontophoresis of acetylcholine, an endothelium-dependent vasodilator, and sodium nitroprusside, an endothelium-independent vasodilator, will occur, the response to which will be recorded using LSCI.
At the study outset, investigators will record additional biophysical parameters such as blood pressure, weight, and BMI. Blood will be drawn and serum analysis of lipid profile, fasting glucose, high sensitivity C-reactive protein, s-Flt-1, platelet-derived growth factor, and uric acid will occur. Urine will be collected for analysis of albumin: creatinine ratio. Findings will then be integrated to calculate a lifetime cardiovascular risk score, which is used to categorize individuals as low risk or high risk.
Study participants who are assigned to the oral aspirin arm of the study will receive 81 mg oral aspirin. Over-encapsulated 81mg aspirin tablets will be used. Study participants in this arm will take 81mg aspirin daily for 6 months. A standard placebo pill, the same size, shape, and color of the oral aspirin will also be used. The placebo will be administered to the participants randomized to the placebo group in the same manner the oral aspirin would be administered - they will take the pill daily for 6 months.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Basic Science
- Masking
- Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Eligibility Criteria
- Sex
- Female
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •Confirmed severe preeclampsia diagnosed prior to delivery
- •Preeclampsia defined as: Blood pressure > 140/90 AND proteinuria > 300mg/24 hours OR 2+ on repeat dip stick
- •Severe Preeclampsia defined as the presence of one or more of the following:
- •i. systolic blood pressure ≥ 160mmHg or diastolic blood pressure ≥ 110 mmHg on 2 occasions at least 4 hours apart
- •ii. new-onset cerebral or visual disturbance
- •iii. severe persistent right upper quadrant pain or serum transaminase concentrations ≥ 2 times the upper limit of normal
- •iv. thrombocytopenia (platelets < 100 x 109/L)
- •v. renal insufficiency (serum creatinine > 97.2 umol/L)
- •vi. pulmonary edema
- •A singleton gestation
- •Gestation between 24+0/7 to 40+6/7 weeks.
Exclusion Criteria
- •Exclusion Criteria:
- •Multiple pregnancy
- •Chronic hypertension or other condition requiring the use of BP-lowering medication
- •Cardiovascular disorders: Unstable angina pectoris, heart failure, life-threatening arrhythmia, atrial fibrillation, kidney failure
- •Known allergy or sensitivity to aspirin used in the study
- •Any medical comorbidity that is a contraindication to LD-ASA: Hemophilia or other bleeding disorder, history of GI bleeding, renal failure, severe liver disease, thrombocytopenia, gout, G6PD deficiency
- •Recent history of drug/alcohol abuse (< 1 year prior to delivery), or receiving treatment for such
- •Nasal polyps
- •Hypercholesterolemia requiring pharmaceutical treatment
- •Raynaud's phenomenon
- •Collagen-vascular disease: lupus, scleroderma, rheumatoid arthritis
- •History of pre-existing diabetes
- •Ongoing use of any of the following medications: methotrexate, anti-coagulants, thrombolytics, oral hypoglycemics, uricsuric agents, valproic acid, glucocorticosteroids, digoxin
Arms & Interventions
PO LD-ASA
Study participants who are assigned to the oral aspirin arm of the study will receive 81mg oral aspirin. Over-encapsulated 81mg aspirin tablets will be used. Study participants in this arm will take 81mg aspirin daily for 6 months.
Intervention: Low-dose aspirin (Drug)
PO Placebo
A standard placebo pill, the same size, shape and color of the oral aspirin will be used. The placebo pills will be over-encapsulated in the same manner as the aspirin tablets. The placebo will be administered to the participants randomized to placebo group in the same manner the oral aspirin would be administered - they will take the pill daily for 6 months.
Intervention: Placebo oral tablet (Drug)
Outcomes
Primary Outcomes
Endothelium-Dependent Dilation
Time Frame: Immediate Postpartum to 6 Months Postpartum
Changes in endothelium-dependent dilation from the immediate postpartum period to 6 months postpartum. Measured by laser speckle contrast imaging in conjunction with iontophoresis.
Secondary Outcomes
- Uric Acid Levels(6 months postpartum)
- Total Cholesterol(6 months postpartum)
- High Density Lipoprotein(6 months postpartum)
- Urine Albumin Creatinine Ratio(6 months postpartum)
- Low Density Lipoprotein(6 months postpartum)
- Triglycerides(6 months postpartum)
- Concentration of Placental Growth Factor(6 months postpartum)
- Blood Pressure(6 months postpartum)
- Body Mass Index(6 months postpartum)
- Concentration of Serum sFlt-1(6 months postpartum)
- Endothelium-Independent dilation(Immediate Postpartum to 6 Months Postpartum)
- High Sensitivity C-Reactive Protein(6 months postpartum)
Investigators
Dr. Graeme Smith
Principal Investigator
Queen's University