Impact of Enoxaparin Therapy on Fetal Outcomes in Intrauterine Growth Restriction

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-40
SponsorMuhammad Aamir Latif

About this trial

The local literature lacks comprehensive information regarding the actual incidence of intrauterine growth restriction (IUGR) and oligohydramnios and currently available therapeutic options. Therefore, the current study was planned with the objective to evaluate the impact of enoxaparin therapy compared with standard management on neonatal outcomes in pregnancies complicated by intrauterine growth restriction (IUGR) with oligohydramnios.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Women aged 18-40 years

Singleton pregnancy

Gestational age ≥28 weeks (confirmed by first-trimester scan or reliable last menstrual period)

Diagnosed with both IUGR and oligohydramnios

Disqualifiers

Multiple gestation

Major fetal congenital anomalies

Maternal medical disorders affecting pregnancy outcome (e.g., uncontrolled diabetes, chronic hypertension, renal disease)

Known coagulation disorders or contraindications to enoxaparin

Trial design

Design model

Parallel

Treatments tested in this trial

  • Enoxaparin

    Drug

    Patients will receive standard management plus enoxaparin 40 mg subcutaneously once daily until delivery

  • Standard Management

    Other intervention

    Patients will continue with standard management alone.

Treatment groups

108 Participants
are divided into 2 treatment groups
Group A: Enoxaparin GroupExperimental treatment 2 interventions
Group B: Standard Management GroupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Live birth

The frequency of live birth will be noted. Delivery of a baby with signs of life at birth, irrespective of gestational age will be considered as live birth.

Time frame
12 weeks
2

Low Birth weight

Frequency of low birth weight will be noted. Neonatal birth weight \<2.5 kg will be documented as low birth weight.

Time frame
12 weeks

Secondary outcomes

1

Neonatal Intensive Care Unit Admission

The frequency of admission to the neonatal intensive care unit will be noted.

Time frame
7 days
2

Perinatal Mortality

Perinatal mortality will be labeled "yes" if there is a stillbirth or neonatal death within the first 7 days of life.

Time frame
7 days

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Muhammad Aamir Latif

Lead sponsor

RESnTEC, Institute of Research

Sponsor institution

This trial is not recruiting at the moment. You can still explore other options: