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Evaluation of Platelet Function in Pregnancy With Multiple Electrode Aggregometry

Multiple Electrode Aggregometry and Platelet Function in Pregnancy

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01881698
Acronym
MULPP
Enrollment
200
Registered
2013-06-20
Start date
2013-10-31
Completion date
2015-05-31
Last updated
2013-10-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Platelet Function, Pregnancy

Keywords

pregnancy, platelet function, monitoring, multiple electrode aggregometry

Brief summary

Establishment of a range of normal values in pregnancy with the Multiple Electrode Aggregometry (Multiplate@) device, a device that allows measurement of not only platelet count but platelet function. This has not been studied in ths special patient group. Results from this trial will be used as a basis for further investigation of abnormal platelet function in pregnancy.

Interventions

OTHERPlatelet function during pregnancy Multiple Electrode Aggregometry (Multiplate@) device

Observation of platelet function in pregnancy

Sponsors

Medical University of Vienna
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* pregnancy

Exclusion criteria

* Rejection of informed consent

Design outcomes

Primary

MeasureTime frameDescription
Change of platelet function4x, as specified belowMeasurement of change of platelet function by the Multiplate® device. First measurement (baseline measurement) at enrollment into the trial. Second measurement during government-mandated gynaecological evaluation, around the 20th week of pregnancy. Third measurement immediately prior to delivery. Last measurement one week after delivery. 2nd, 3rd and 4th measurement for assessment of change from baseline.

Secondary

MeasureTime frameDescription
Platelet-associated complications4x, as specified below (baseline, 20th week)Record of bleeding events, preeclampsia, HELLP (hemolysis, elevated liver enzymes, and low platelet count) syndrome. Time points: at every assessment of primary outcome measure, as described above.

Countries

Austria

Contacts

Primary ContactReinhard Hahn, MD
reinhard.hahn@meduniwien.ac.at0043 1 40400
Backup ContactAlbert M de Bettignies
n0826451@students.meduniwien.ac.at0043 1 40400

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026