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Prevention of Preeclampsia With Aspirin in Recipients of Donated Oocytes.

Prevention of Preeclampsia With Aspirin Administered From the Beginning of Pregnancy in Recipients of Donated Oocytes.

Status
Terminated
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02174328
Acronym
PROVAS
Enrollment
81
Registered
2014-06-25
Start date
2014-05-21
Completion date
2018-04-20
Last updated
2019-04-26

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

Conditions

Pre-Eclampsia

Keywords

See incidence of Pre-Eclampsia in acetylsalicylic acid group, See incidence of Pre-Eclampsia in placebo group

Brief summary

The main objective of this trial is to study the occurrence of preeclampsia in recipients of donated oocytes receiving aspirin at an early stage during pregnancy and to compare the results with those obtained in patients receiving placebo.

Detailed description

Various markers have been proposed for the early diagnosis of preeclampsia: determination of mean arterial pressure; presence of multiple risk factors of preeclampsia; biochemical, ultrasound, and angiogenic markers; uterine artery Doppler, etc. These are used to determinate which patients have an increased risk of developing preeclampsia during gestation, and therefore carry out closer monitoring of pregnancy in this population. In addition, these markers can also identify patients at increased risk of developing other problems such as IUGR or preterm labor. For nearly 30 years, there have been multiple studies trying to demonstrate that aspirin prevents the onset of preeclampsia with inconclusive results. However, recent studies in which aspirin was administered at an early stage (before 16 weeks of gestation) in patients at high risk of complications, have demonstrated a decrease in the incidence of this entity. Thus, administration of aspirin to patients at high risk (patients classified with a high risk of complications during pregnancy, based on markers mentioned above) seems to be useful in preventing onset of preeclampsia, IUGR and other complications, whenever it is administered at an early stage, as shown by several studies carried out so far. The incidence of preeclampsia, IUGR and other complications of pregnancy is increased in patients undergoing treatment for ovulation induction, being much higher in recipients of donated oocytes. It appears that this increase may be explained by immunological processes. The focus lies on the interaction between HLA-C fetal antigen with the maternal natural killer cells. We postulate, therefore, that the administration of aspirin in recipients of donated oocytes at an early stage of pregnancy, may also reduce the incidence of preeclampsia in this group of patients. Moreover, it has been observed that patients with preeclampsia exhibit lower levels of VEGF, PlGF and PAPP-A (factors involved in placental angiogenesis) and that this is accompanied by an increase in the sFlt1 (a potent PIGF and VEGF antagonist).

Interventions

DRUGAcetylsalicylic acid

Acetylsalicylic acid once a day until 36 week

DRUGPlacebo

Placebo once a day until 36 week

Sponsors

Instituto de Investigacion Sanitaria La Fe
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* Patients over 18 years. * Recipients of donated oocytes. * Pregnant women. * Single or twin gestations. * Patients who accept the conditions of the study by signing the appropriate informed consent.

Exclusion criteria

* Known allergy to acetylsalicylic acid . * Personal history of peptic ulcer. * Triplets. * Use of prostaglandin inhibitors within 10 days prior to baseline. * Personal history of chronic kidney, thyroid, liver or heart disease. * Psychiatric or cognitive pathology that prevents understanding of the conditions of informed consent.

Design outcomes

Primary

MeasureTime frameDescription
Occurrence of preeclampsia.Up to 42 weeksThe main objective is to study the occurrence of preeclampsia in recipients of donated oocytes receiving aspirin at an early stage during pregnancy, and to compare the results with those obtained in patients receiving placebo.

Secondary

MeasureTime frameDescription
Other complicationsUp to 42 weeksDetermine the development of gestational hypertension, severe preeclampsia, IUGR, and preterm delivery in this group of patients.

Other

MeasureTime frameDescription
Inflammatory mediators involved in angiogenesis.Up to 42 weeksAnother objective is to determine if aspirin, through blockade of cyclooxygenase-2, could act in addition to reducing the synthesis of thromboxane 2, altering or diminishing the formation of various inflammatory mediators involved in angiogenesis.

Countries

Spain

Outcome results

None listed

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