Skip to content

The effect of Aspirin in pregnancy outcome in patients with abnormal down syndrome blood tests and normal karyotype

Evaluation of the effect of Aspirin in pregnancy outcomes in patients with abnormal down syndrome biochemical tests and with normal karyotype

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014120620218N1
Enrollment
85
Registered
2015-01-03
Start date
2014-04-21
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

pregnancy. Fetus and newborn affected by maternal factors and by complications of pregnancy, labour and delivery

Interventions

Intervention 1: In intervention group: Administration of 80 mg Aspirin tablet daily until 34th week of gestation. Intervention 2: control group: no aspirin administration.
Treatment - Drugs
In intervention group: Administration of 80 mg Aspirin tablet daily until 34th week of gestation.
control group: no aspirin administration.

Sponsors

Vice chancellor for research, Kerman University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: pregnant women with abnormal biochemical tests in second trimester which have normal karyotype; consent of the patients. Exclusion criteria: history of sensitivity to aspirin; asthma; Peptic ulcer; renal failure; gout; multifetal pregnancy; gestational diabetes; hemorrhage in first half of pregnancy; maternal disorders; congenital anomalies.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Preterm labor. Timepoint: at birthday. Method of measurement: calculated from the number of completed weeks since the first day of the mother's last menstrual period to the date of birth.;Fetal death. Timepoint: during pregnancy. Method of measurement: examination of fetus.;Intra uterine Growth Restriction. Timepoint: after delivery. Method of measurement: based on age and weight.;Preeclampsia. Timepoint: every two weeks. Method of measurement: patient visit and blood pressure checking.;Placental abruption. Timepoint: at birthday. Method of measurement: examination of fetus.

Secondary

MeasureTime frame
Oligohydramnios. Timepoint: during pregnancy. Method of measurement: examination of fetus.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactManijeh Assaran

Kerman University of Medical Sciences

m.assaran1356@gmail.com00

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026