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NCT04267783

Prediction of Uterine Atony After Vaginal Delivery by Elastography

Completed Last updated 2 September 2020
What this trial tests

trial testing Shear wave elastography in Postpartum Hemorrhage in 30 participants. Completed in 30 May 2020.

Timeline
1 May 2019
Primary endpoint
30 April 2020
30 May 2020

Quick facts

Lead sponsorCentre Hospitalier Universitaire Vaudois
StatusCompleted
Study typeOBSERVATIONAL
Enrollment30
Start date1 May 2019
Primary completion30 April 2020
Estimated completion30 May 2020
Sites1 location across Switzerland

Drugs / interventions tested

Conditions studied

Sponsor

Centre Hospitalier Universitaire Vaudois

Who can join

Adults 18 to 35, female only, with Postpartum Hemorrhage. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Prospective study evaluating the feasibility of shear-wave elastography of the uterus during the third stage of labour and following placental delivery. The investigators hypothesize that the stiffness of the myometrium can be measured by using shear-wave technology. This study involves 30 patients with a healthy pregnancy and spontaneous vaginal delivery. One co-investigator will carry out measurements at the uterine fundus, at three different time points: after fetal delivery, after placental delivery and 30 minutes after placental delivery.

Publications & conference data

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

Verify or expand the search:

Other trials of Shear wave elastography

Trials testing the same drug.

Other recruiting trials for Postpartum Hemorrhage

Currently open trials in the same condition.

Other Centre Hospitalier Universitaire Vaudois trials

Trials by the same sponsor.

Verify against primary sources

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/NCT04267783.

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