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NCT Number: NCT06539975

Effectiveness of Evening Primrose Oil for Induction of Labor

Effectivness of primrose oil in induction of labour .

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Key information

Conditions

Age range

18 year–35 year

Sex eligibility

Female

Study type

Interventional

Phase

Early Phase 1

About this study

Using primrose oil in addition to misoprostol for induction of labor in one group of pregnant women and compare the result with those of another group in which we are using misoprstol only.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • pregenent of 38 weeks and longer
  • singleton pregenency
  • vertex presentation
  • indication of labor induction
  • bishop score <6 and cervical dilation<2 cm

Exclusion criteria

  • women who delivered by classical cs or had a history of myomectomy , hysterscopic uterine surgery , or cervical surgery like conisation
  • women with multiple gestation
  • women with evidence of low implanted placenta by ultrasound
  • women with contraindication to misoprostol or vaginal delivery

Treatment and study plan

Evening Primrose Oil 1000 MG

Drug

Evening primrose oil 1000mg vaginally plus misoprostal for induction of labor

Primary outcomes

  1. The interval between induction of labor and delivery

    Time frame: induction of labor may take more than 24 hours

    comparing between the interval between induction of labor and delivery in two groups one is using evening primrose oil + misoprostol and the other using misoprostol only.

Study contacts

Contact information is provided by the study sponsor or research team.

Abdelrhaman abdelkader, DR

CONTACT

[email protected]

01094628728

sayed mohamed, resident

CONTACT

[email protected]

01093622038

Sponsors and collaborators

Lead sponsor

Assiut University

Other

Registry information

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Aug 6, 2024
Registry last updated
Aug 6, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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