Skip to content

Measuring Uterine Electrical Activity Throughout Pregnancy and Labor Measuring Uterine Electrical Activity Throughout Pregnancy and Labor

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01165879
Enrollment
100
Registered
2010-07-20
Start date
2010-05-31
Completion date
Unknown
Last updated
2011-06-10

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

Conditions

Pregnancy

Keywords

Pregnancy, Term, Preterm, Uterine Contractions

Brief summary

The EUM100pro (Electrical Uterine Monitor)is a uterine contraction monitor which measures uterine contractions based on the electrical activity of the uterine muscle.The study will compare the EUM100pro measurements to the already existing uterine contractions monitors (tocodynamometer and Intra Uterine Pressure Catheter) in pregnant women with complaints of uterine contractions.

Detailed description

The main objective of the study is to demonstrate that the EUM100pro is as good as the current methods for monitoring pregnancy in labor (tocodynamometer, IUPC) in measuring uterine contractions. This will be performed by measuring the expectancy of time differences between the tocodynamometer/IUPC and the EUM in the beginning, end, peak and duration of each contraction. A good correlation will be 0.9 and significance of 95%. 100 women will be recruited to the study. The measurement with the EUM100pro will not interfere with the usual clinical care, meaning- the EUM100pro will be used in addition to the standard care and monitoring.

Interventions

None listed

Sponsors

OB-Tools Ltd.
Lead SponsorINDUSTRY

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Women at term with complaint of uterine contractions at Meir Medical Center * Women at preterm with complaint of uterine contractions at Meir Medical Center. * Women at gestational age \>24 weeks * Subjects who understood, agreed and signed the informed consent form

Exclusion criteria

* Subjects who refused to sign the informed consent form * Abnormal fetal heart rate recording at admittance * Subjects with indications for immediate delivery * Subjects younger than 18 years of age * Subjects at gestational age \<24 weeks

Design outcomes

Primary

MeasureTime frameDescription
The study primary outcome is to demonstrate that the EUM100pro uterine contractions measurements is as good as the current methods for monitoring pregnancy in labor (tocodynamometer, IUPC).two yearsThe primary outcome will be measured by correlation of timing of :peak display in beginning, during and end of peak in the EUM100pro versus the timing of the peak display in beginning, during and the end tocodynamometer and or IUPC peak.
To evaluate patient safetyone yearMeasurements of device related adverse events throughout the study.

Secondary

MeasureTime frameDescription
Correlation of uterine contractions intensity between EUM100pro and Intra Uterine Pressure Catheter measurements.one yearThe secondary outcome will investigate a correlation between the intensity/peak of contraction of mechanical contraction as measured by Intra Uterine pressure catheter and the intensity/peak of contraction of electrical activity as measured by the EUM exists.
To evaluate usability of the EUM100proone year
to evaluate whether a fetal ECG can be exctraced from the electrical signal of the uterus.one yearThe electrical signal recorded from the abdomen thechnically contain the uterine muscle electrical activity but also the electrical signal from the fetal ecg.

Countries

Israel

Contacts

Primary ContactTal Shental Biron, MD
Tal.Biron-Shental@clalit.org.il972-577482716

Outcome results

None listed

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