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NCT03266432: DIC

Thromboelastometry Guided DIC Prevention After Cesarean Section in Pregnant Women With Placenta Previa

Status unknown NA Last updated 10 July 2019
What this trial tests

NA trial testing blood samples in DIC Syndrome in 60 participants. Status unknown.

Timeline
28 August 2017
Primary endpoint
30 June 2020
30 June 2020

Quick facts

Lead sponsorAssiut University
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposeprevention
Enrollment60
Start date28 August 2017
Primary completion30 June 2020
Estimated completion30 June 2020
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Assiut University

Who can join

Adults 18 to 45, female only, with DIC Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Evaluation of the use of thromboelastometry for early identification of the underlying coagulopathy and to guide individualized transfusion therapy to prevent DIC development during ICU stay after cesarean section in women with placenta previa who require a massive blood transfusion.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of blood samples

Trials testing the same drug.

Other Assiut University 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/NCT03266432.

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