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Efficacy of Aspirin and L-arginine in High Risk Preeclamptic

Efficacy of the Combination of Acetylsalicylic Acid and L-arginine to Prevent Preeclampsia in Pregnant High Risk

Status
Suspended
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02838030
Enrollment
82
Registered
2016-07-20
Start date
2018-07-01
Completion date
2021-08-31
Last updated
2020-11-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

High Risk Pregnancy

Keywords

Preeclampsia, L-arginine

Brief summary

Worldwide, the incidence of preeclampsia ranges from 2 to 10% of pregnancies. The World Health Organization (WHO) estimates that the incidence of preeclampsia is seven times higher in developing countries than in developed (2.8% and 0.4%). In Mexico it is estimated that preeclampsia - eclampsia is a major cause of maternal and perinatal morbidity and mortality. Because it is an idiopathic heterogeneous syndrome associated with endothelial damage, so far there is no effective treatment to decrease the morbidity and mortality of this entity, so it is necessary to strengthen prevention; the use of aspirin alone is inconclusive, in addition to the information the investigators have reduced the effect of these strategies on arterial stiffness; Moreover, it has been observed that L-arginine lowers blood pressure in this population. It is for this that is of interest to know the efficacy and safety of the combination of L-arginine low dose, which is known as an important eNOS in NO production substrate, and aspirin for its qualities of antiinflammatory and anticoagulant in the prevention of preeclampsia and also determine their effect on arterial stiffness as a noninvasive method, as is the applanation tonometry.

Detailed description

It will conduct a clinical trial, double-blind, randomized and placebo control group female patients with 12 weeks of gestation have one or more risk factors for developing preeclampsia. 2 groups will be formed with 82 patients each, chance will determine the intervention (acetylsalicylic + L-arginine acetylsalicylic acid or acid + placebo). At the beginning and end of the intervention clinical and laboratory determinations, the end will be determined in both groups the incidence of preeclampsia, severity and number needed to treat is made. The data obtained were analyzed using SPSS statistical software version 22. It was considered statistically significant at p \<0.05.

Interventions

DRUGL-arginine

3 gr per day

DRUGPlacebo (for L-arginine)

3 gr per day

DRUGacetylsalicylic acid

3 gr per day

Sponsors

PhD Ernesto Javier Ramírez Lizardo
CollaboratorUNKNOWN
PhD Sylvia Elena Totsuka Sutto
CollaboratorUNKNOWN
PhD Fernando Grover Páez
CollaboratorUNKNOWN
MD Diego Hernández Molina
CollaboratorUNKNOWN
University of Guadalajara
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 44 Years
Healthy volunteers
No

Inclusion criteria

* Pregnant before 12 weeks of gestation * High risk of preeclampsia * Signature of informed consent in writing

Exclusion criteria

* Noncompliance \> 20% of drug intake * Lack of tolerability L-arginine or acetylsalicylic acid * Compliance with at least one non-inclusion criteria during the course of the study * Serious adverse event * Withdrawal of consent

Design outcomes

Primary

MeasureTime frame
Incidence of preeclampsiafrom 20 weeks gestation until 37 weeks
severity of preeclampsiafrom 20 weeks gestation until 37 weeks

Secondary

MeasureTime frame
Stroke maternalat week 37
Acute respiratory distress syndrome maternalat week 37
Coagulopathy maternalat week 37
Renal failure maternalat week 37
Retinal damage maternalat week 37
maternal mortalityat week 37
Birth weightbirth
Pulmonary edema maternalat week 37
Fetal mortalitybirth
systolic blood pressure maternalfrom 12 weeks gestation until 37 weeks
diastolic blood pressure maternalfrom 12 weeks gestation until 37 weeks
Mean blood pressure maternalfrom 12 weeks gestation until 37 weeks
Pulse wave velocity maternalfrom 12 weeks gestation until 37 weeks
Adverse effects maternalfrom 12 weeks gestation until 37 weeks
Intrauterine growth restrictionbirth
Acute myocardial infarction maternalat week 37

Countries

Mexico

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026