Chronic Hypertension and Acetyl Salicylic Acid in Pregnancy (CHASAP)

Chronic Hypertension and Acetyl Salicylic Acid in Pregnancy, a Multicenter Prospective Randomized Double-blind Placebo-controlled Trial.

A randomized clinical trial to assess the efficiency of acetylsalicylic acid (aspirin) 150 mg/day started before 20 weeks of gestation in the prevention on maternal and fœtal complications in pregnant women with chronic hypertension.

Study Overview

• Status: Recruiting
• Conditions: Aspirin; Pre-Eclampsia; Intrauterine Growth Restriction; Perinatal Death; Placental Abruption; Chronic Hypertension Complicating Pregnancy
• Intervention / Treatment: Drug: Aspirin 150 mg; Drug: Placebo

Detailed Description

Chronic hypertension affects 1 to 5% of women of childbearing age. According to the literature, about 45% of pregnant women with chronic hypertension will develop complications such as superimposed preeclampsia (PE), placental abruption, Intra Uterine Growth Restriction (IUGR), perinatal death, maternal death, or preterm delivery. To date, there is no curative treatment of vascular complications of chronic hypertension during pregnancy. The only effective treatment, once the complications are established, is usually stopping the pregnancy and delivering the placenta. The preventive treatment of these complications is therefore an important axis in the improvement of maternal and perinatal health.

Due to the very high risk of superimposed PE in chronic hypertensive patients and despite the lack of objective evidence of the effectiveness of low-dose aspirin in the prevention of superimposed PE in this population, the NICE (National Institute for Health and Care Excellence), associated with the Royal College of Gynecology-Obstetrics, recommends since 2010-2011 the use of low-dose aspirin in the prevention of this complication in chronic hypertensive pregnant women; then it was followed by the "U.S. Preventive Services Task Force (USPTF)" in 2014. Recently, the American College of Obstetrics and Gynecology (ACOG) adopted the suggestions of the USPTF and issued the same recommendations in 2018. The French college of obstetric (CNGOF: National College of French Gynecologists and Obstetricians), however, does not recommend the use of low-dose aspirin in pregnant chronic hypertensive women because of insufficient data.

Indeed, although the efficacy of low-dose aspirin is assumed in patients with previous PE, few studies have evaluated its efficacy in patients with chronic hypertension. Moreover, most of the controlled prospective studies using very low doses of aspirin (less than 100 mg) and starting after 20 weeks of gestation do not seem conclusive. For these reasons, the investigators propose to conduct a prospective randomized double-blind placebo-controlled trial to analyze the effectiveness of aspirin dosed at 150 mg and introduced before 20 weeks of gestation in women with chronic hypertension.

The primary endpoint is a maternal and perinatal composite morbidity and mortality including superimposed PE, intrauterine growth restriction, preterm delivery < 37 weeks of gestation, placental abruption, perinatal death, or maternal death.

The definition of superimposed PE in our study is the appearance of significant proteinuria in a chronic hypertensive pregnant woman.

In a secondary analyze, the statistician will use the new definition of superimposed PE that does not require the mandatory presence of proteinuria but the association of chronic hypertension and the appearance of neurological signs (eclampsia, persistent headache, visual disturbances, severe nausea or vomiting), pulmonary edema, persistent epigastric pain, thrombocytopenia <100000 platelets/µL, liver enzymes at 2 times normal, renal insufficiency ( serum creatinine ≥ 97 μmol/L or 1.1 mg/dL,) or a doubling of serum creatinine in the absence of chronic renal disease or significant proteinuria after 20 weeks of gestation or postpartum.

Significant proteinuria is defined as greater than 300 mg/24 hours or when the ratio proteinuria/ creatininuria is ≥ 30 mg/mmol (ratio to 0.3 if all are in mg/dL), in a non-proteinuric women with no urinary tract infection.

• Study Type: Interventional
• Enrollment (Estimated): 500
• Phase: Phase 3

Contacts and Locations

• Study Contact: Name: Camille JUNG; Phone Number: +33 01 45 17 50 00; Email: camille.jung@chicreteil.fr
• Study Contact Backup: Name: Edouard LE CARPENTIER; Phone Number: +33 01 45 17 50 00; Email: Edouard.Lecarpentier@chicreteil.fr

Study Locations

• France
  • Bordeaux, France
    • Recruiting
    • CHU Bordeaux
    • Contact: Loïc SENTILHES
  • Caen, France, 14000
    • Withdrawn
    • CHU caen
  • Clamart, France
    • Recruiting
    • CHU Antoine Béclère, AP-HP
    • Contact: Alexandra BENACHI
  • Colombes, France
    • Recruiting
    • Hôpital Louis Mourier, AP-HP
    • Contact: Jeanne SIBIUDE
  • Créteil, France, 94000
    • Recruiting
    • Centre Hospitalier Intercommunal de Créteil
    • Contact: Edouard LECARPENTIER, Ph; Phone Number: +33 01 57 02 50 00; Email: edouard.lecarpentier@chicreteil.fr
  • Dijon, France
    • Recruiting
    • CHU Dijon
    • Contact: Emmanuel SIMON
  • Le Kremlin-Bicêtre, France
    • Recruiting
    • CHU Bicêtre, AP-HP
    • Contact: Claire SZMULEWICZ
  • Lille, France
    • Not yet recruiting
    • CHRU Lille
    • Contact: Louise GHESQUIERE
  • Lyon, France
    • Recruiting
    • CHU LYON
    • Contact: Jérôme MASSARDIER
  • Marseille, France
    • Withdrawn
    • Hôpital St Joseph
  • Nancy, France
    • Withdrawn
    • CHRU Nancy
  • Nantes, France
    • Recruiting
    • CHU Nantes
    • Contact: Norbert WINER
  • Paris, France
    • Recruiting
    • CHU Cochin- Port Royal, AP-HP
    • Contact: Vassilis TSATSARIS
  • Paris, France
    • Recruiting
    • CHU Robert Débré, AP-HP
    • Contact: Diane KORB
  • Paris, France
    • Recruiting
    • Hôpital Trousseau, AP-HP
    • Contact: Pierre DELORME
  • Paris, France
    • Recruiting
    • CHU Tenon
    • Contact: Anne-Gaël CORDIER
  • Poissy, France
    • Recruiting
    • CH Poissy
    • Contact: Paul BERVEILLER
  • Saint-Étienne, France
    • Recruiting
    • CHU St Etienne
    • Contact: Tiphaine BARJAT
  • Toulouse, France
    • Not yet recruiting
    • CHU Toulouse
    • Contact: Paul GUERBY
  • Tours, France
    • Withdrawn
    • Chu Tours

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• Pregnant patient between 10 and 19 weeks of gestation + 6 days
• Chronic hypertension, whether treated or not, know before pregnancy or diagnosed before randomization
• Singleton pregnancy
• Signed the written informed consent
• Affiliation to social security

Exclusion Criteria:

• ---Medical history requiring anticoagulation (antiphospholipid syndrome, deep vein thromboembolic disease, pulmonary embolism, atherothrombosis, patient with mechanical heart valves),
• Patient receiving aspirin for another indication outside pregnancy,
• Patient with significant proteinuria (> 300mg/24 hours or a proteinuria/creatininuria ratio ≥ 30mg/mmol),
• Active bleeding,
• History of severe PE with delivery < 34 weeks of gestation,
• Hypersensitivity to salicylates such as aspirin and other nonsteroidal anti-inflammatory drugs (NSAIDs),
• Platelet count lower than 100,000 cells/microliter (dosage less than 6 months old),
• Hemostasis disorders, including hemophilia (with thrombocytopenia)
• Any constitutional or acquired hemorrhagic disease, (including digestive hemorrhages, history of hemorrhagic stroke and thrombocytopenia
• Human immunodeficiency virus, or hepatitis B virus, or hepatitis C virus positive serum,
• Patient included in another interventional study which could interfere with the results of the study,
• Age <18 years old,
• Women under the protection of justice,
• Patients with psychiatric follow-up, poor understanding of French or cognitive problems,
• Duodenal ulcer,
• Severe renal impairment,
• Severe hepatic insufficiency,
• Severe cardiac impairment,
• Gout,
• Patients with known glucose-6-phosphate dehydrogenase deficiency,

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Triple

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Aspirin 150 mg; Aspirin 150 mg / day (acetylsalicylic acid) once daily in the evening	Drug: Aspirin 150 mg; Treatment assigned by randomization will be prescribed immediately and continued throughout pregnancy up to 35 weeks + 6 days for both groups. The active or placebo will be dispensed by the centre's pharmacy. Treatment will be taken in the evening. A daily log is given to patients and must be completed every day.; Other Names: Active arm
Placebo Comparator: Placebo; Placebo taken in the evening	Drug: Placebo; Treatment assigned by randomization will be prescribed immediately and continued throughout pregnancy up to 35 weeks + 6 days for both groups. The active or placebo will be dispensed by the centre's pharmacy. Treatment will be taken in the evening. A daily log is given to patients and must be completed every day.; Other Names: comparator arm

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Composite morbidity-mortality criterion including preeclampsia, intra-uterine growth retardation <10th percentile, placental abruption, Preterm birth < 37 weeks of gestation, Perinatal death, Maternal death	A composite morbidity-mortality criterion that includes the occurrence during pregnancy or postpartum of at least one of the following events: preeclampsia, IUGR <10th percentile, placental abruption, Preterm birth < 37 weeks of gestation, Perinatal death (death from 22 weeks of gestation until 28 days after birth), Maternal death	9 months

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
IUGR (< 10th percentile of birth weight)	Rate of IUGR (< 10th percentile of birth weight)	9 months
Placental abruption	Rate of placental abruption	9 months
Preterm birth < 37 weeks of gestation	Rate of severe preterm delivery (< 37 weeks of gestation)	9 months
Maternal death	Rate of severe maternal death	9 months
Severe pre-eclampsia	Rate of severe pre-eclampsia. Concerning the rate of superimposed PE, it will be analyze according the two definition specified in the rational	9 months
Intrauterine growth restriction (IUGR)	Rate of severe IUGR (< 5th percentile of birth weight)	9 months
Preterm delivery	Rate of severe preterm delivery (< 34 weeks of gestation)	8 months
Fetal loss	Rate of fetal loss (fetal loss between 10 and 21 weeks of gestation)	5 months
Fetal death	Rate of fetal death (fetal death from 22 weeks of gestation until delivery)	5 months
Neonatal death	Rate of neonatal death (death from birth until 28 days)	9 months
Neonatal morbidity	Neonatal morbidity (stay in a neonatal intensive care unit, assisted ventilation > 24 hours, hyaline membrane disease, intraventricular hemorrhages stage III or IV)	9 months
Toxicity of aspirin	Potential toxicity of the treatment: major maternal bleeding event (active externalized, intracranial, intra-ocular, retroperitoneal, articular), or minor,	8 months
Adherence	Adherence of treatment (diary) and its relationship with the efficacy of the preventive effect on primary outcome,	8 months
Biological response to the treatment	Response to the treatment by a urine thromboxane assay	4 months
Angiogenic profile	Circulating and urinary angiogenic profile associated with maternal and fetal clinical data: sFLT1 ( Soluble fms-like tyrosine kinase-1)(serum and urine), PlGF ( Placental Growth Factor)(serum and urine)	9 months
Child development	Child psychomotor development and health problems at 2 years of age	2 years
Child development	Child psychomotor development and health problems at 4 years of age	4 years
Subgroups analysis	Rate of the composite morbidity-mortality criterion in 2 subgroups: treatment started before or after 15 SA	9 months

Collaborators and Investigators

• Sponsor: Centre Hospitalier Intercommunal Creteil

Study record dates

Study Major Dates

• Study Start (Actual): February 15, 2021
• Primary Completion (Estimated): February 1, 2026
• Study Completion (Estimated): February 1, 2030

Study Registration Dates

• First Submitted: April 19, 2020
• First Submitted That Met QC Criteria: April 21, 2020
• First Posted (Actual): April 22, 2020

Study Record Updates

• Last Update Posted (Actual): September 26, 2023
• Last Update Submitted That Met QC Criteria: September 25, 2023
• Last Verified: September 1, 2023

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Pathologic Processes; Cardiovascular Diseases; Vascular Diseases; Fetal Diseases; Obstetric Labor Complications; Placenta Diseases; Death; Hypertension, Pregnancy-Induced; Growth Disorders; Female Urogenital Diseases and Pregnancy Complications; Urogenital Diseases; Hypertension; Eclampsia; Pre-Eclampsia; Fetal Growth Retardation; Pregnancy Complications; Perinatal Death; Abruptio Placentae; Physiological Effects of Drugs; Molecular Mechanisms of Pharmacological Action; Peripheral Nervous System Agents; Enzyme Inhibitors; Analgesics; Sensory System Agents; Anti-Inflammatory Agents, Non-Steroidal; Analgesics, Non-Narcotic; Anti-Inflammatory Agents; Antirheumatic Agents; Fibrinolytic Agents; Fibrin Modulating Agents; Platelet Aggregation Inhibitors; Cyclooxygenase Inhibitors; Antipyretics; Aspirin
• Other Study ID Numbers: CHASAP; 2018-004160-58 (EudraCT Number)

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No