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The Treatment of Magnesium Sulfate and Nifedipine in Preterm Labor Threat (MgSO4)

K

Konya Meram State Hospital

Status

Enrolling

Conditions

Pregnancy Preterm
Preterm Labor Without Delivery

Treatments

Drug: Nifedipine
Drug: Magnesium sulfate

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Comparison of the effects of Nifedipine and MgSO4 therapies on maternal and fetal blood flow.

Full description

In this study, the investigators aim to compare the effect of Nifedipine and MgSO4 therapies on Doppler parameters of the uterine, umbilical, middle cerebral arteries, and ductus venous in the first 48 hours of therapy in pregnancies with preterm labor threat and also compare perinatal outcomes after delivery between the groups.

Enrollment

30 estimated patients

Sex

Female

Ages

18 to 38 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • pregnancies with preterm labor threat between 28-34 weeks gestational ages

Exclusion criteria

  • Cervical dilatation at > 4 cm and/or cervical effacement >80%,
  • Multiple pregnancies,
  • Pregnancy complications including preeclampsia, ablatio placenta, intrauterine growth restriction, placenta previa, gestational diabetes

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

30 participants in 3 patient groups

Magnesium sulfate treatment
Active Comparator group
Description:
A total of 30 pregnancies with preterm labor threats will be treated with Magnesium sulfate.
Treatment:
Drug: Magnesium sulfate
Nifedipine treatment
Active Comparator group
Description:
A total of 30 pregnancies with preterm labor threats will be treated with Nifedipine.
Treatment:
Drug: Nifedipine
Healthy pregnant women
No Intervention group
Description:
A total of 30 pregnancies without preterm labor threat will be included.

Trial contacts and locations

1

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Central trial contact

Merve Turk

Data sourced from clinicaltrials.gov

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