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Vaginally Administered Versus Per Oral Misoprostol in Induction of Labour | Clinical Trials | Clareo Health

COMPLETEDPhase 4NCT02539199

Vaginally Administered Versus Per Oral Misoprostol in Induction of Labour

The purpose of this study is to investigate the effectiveness and safety of vaginally administered misoprostol (Misodel) versus per orally administered misoprostol (Cytotec) in induction of labour in ...

Lead sponsor: Tampere University Hospital•5 locations•View source on ClinicalTrials.gov

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: April 18, 2018Terms

Trial snapshot

StatusCOMPLETED

PhasePHASE4

Enrollment270

Start dateSep 2015

Last updatedApr 18, 2018

Condition

Labour Induction

Locations shown

Helsinki University hospital

Helsinki

Kuopio University Hospital

Kuopio

Oulu University Hospital

Oulu

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: April 18, 2018Data synced to Clareo: June 28, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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