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Effect of Maternal Age and BMI on Induction of Labor Using Oral Misoprostol in Late-term Pregnancies: a Retrospective Cross-sectional Study

U

University of Palermo

Status

Not yet enrolling

Conditions

Induction of Labor Affected Fetus / Newborn
Pregnancy Late

Treatments

Drug: Misoprostol

Study type

Observational

Funder types

Other

Identifiers

NCT06184139
MISO-LATE_PREG

Details and patient eligibility

About

To evaluate the effect of maternal age and body mass index (BMI) on oral misoprostol induction of labor for late-term pregnancies.

Enrollment

104 estimated patients

Sex

Female

Ages

18 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Late term pregnancies out of labor,
  • Bishop score < 7

Exclusion criteria

  • labor (defined as presence of at least three painful uterine contractions every ten minutes),
  • uterine tachysystole (>5 contractions within 10 minutes for two consecutive 10-minute periods),
  • hypertonic uterus,
  • abnormal CTG,
  • contraindications to vaginal delivery (fetal malpresentation such as breech presentation or transverse situation, fetal macrosomia, abnormally implanted placenta, active genital herpes infection, cervical cancer),
  • patients with parity > 4,
  • medical contraindication to misoprostol (asthma, glaucoma),
  • women with previous hysterotomies.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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