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Clinical Trials/PACTR202308710880623
PACTR202308710880623Not yet recruitingUnknown

Assessment of the effect of intravenous dexamethasone use on pre-induction cervical parameters and induction of labour outcomes:a randomized controlled study.

Oyenmwen Amadasun0 sites108 target enrollmentStarted: July 7, 2023Last updated:
Conditions

Trial Snapshot

Phase
Unknown
Status
Not yet recruiting
Sponsor
Enrollment
108

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
19 Year(s) to 44 Year(s) (—)
Sex
Female

Inclusion Criteria

  • Nulliparity
  • Gestational age of pregnancy of 39 to 42 weeks
  • Unfavourable Bishop score of less than 6
  • Singleton pregnancy
  • Cephalic presenting fetus
  • Normal amniotic fluid
  • Reassuring cardiotocograph
  • No congenital foetal anomaly

Exclusion Criteria

  • Maternal medical conditions example, hypertension, preeclampsia, hyperglyaemic states
  • Fetal macrosomia
  • Multiple gestation
  • Breech presentation of foetus
  • History of rupture of membranes
  • Previous uterine surgery, previous caesarean section
  • Women who do not give consent
  • Women with favourable Bishop score of more than 6

Investigators

Sponsor
Oyenmwen Amadasun

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