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NCT00540748: oxystudien

Is Oxytocin Given During Surgical Procedure for Abortion Before 12 Weeks of Pregnancy Useful ?

Completed NA Last updated 15 April 2010
What this trial tests

NA trial testing oxytocin in Induced Abortion in 400 participants. Completed in 1 December 2009.

Timeline
1 October 2007
Primary endpoint
1 June 2009
1 December 2009

Quick facts

Lead sponsorAsker & Baerum Hospital
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment400
Start date1 October 2007
Primary completion1 June 2009
Estimated completion1 December 2009
Sites1 location across Norway

Drugs / interventions tested

Conditions studied

Sponsor

Asker & Baerum Hospital

Who can join

Adults 18 to 45, female only, with Induced Abortion. Healthy volunteers can join.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

This is a randomized, single-blind study using oxytocin 5U i.v. during surgical abortion in one arm of the study, and no medication in the other arm of the study. Comparison is done between the two groups measuring the following outcomes: pain, nausea and blood loss. The investigators' hypothesis is that there will be no significant differences between the two groups.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other trials of oxytocin

Trials testing the same drug.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00540748.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing