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Maternal Oral Hydration and External Cephalic Version

U

University of Milano Bicocca

Status

Completed

Conditions

External Cephalic Version
Maternal Oral Hydration

Treatments

Other: hydration

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The investigators are carrying out a study of 164 pregnant women, with breech presentation at term who will undergo to external cephalic version. The investigators' goal is to know if oral maternal hydration can increase the successful of external cephalic version

Enrollment

164 patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • single gestation
  • breech presentation
  • from 37 to 41,5 weeks
  • without pregnancy complications
  • fetus adequate for gestational age
  • without fetal malformations
  • intact membranes
  • amniotic fluid index between 7 and 24 cm
  • placenta properly inserted

Exclusion criteria

  • age less than 18 years
  • maternal disease at risk of fluid overload (cardiac disease, renal impairment, moderate or severe preeclampsia or hypertension and diabetes)
  • contraindications for vaginal birth
  • vaginal blood loss
  • uterine contractions

Trial design

164 participants in 2 patient groups

hydration
Experimental group
Description:
after recruitment the women in hydration group will be invited to drink 2 litres of water,in 2 hours
Treatment:
Other: hydration
control
No Intervention group

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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