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Clinical Trial Summary

The main aim of the study is to compare the clinical performance of two adjunctive methods to CTG in intrapartum fetal monitoring: FBS with measurement of scalp lactate and ST analysis of the fetal ECG.


Clinical Trial Description

We use Lactate as a standard adjunctive method in our hospital but we have STAN software available ( is demasked) in our CTG monitors. We will include all women in labour with an intern scalp monitoring and analyse the CTG, the lactate samples and the STAN signals in the same patient and - Study the relationship between the decision-to-delivery interval and neonatal morbidity in deliveries monitored by scalp lactate measurement - Compare the diagnostic capability of both methods to identify fetuses at risk of hypoxia - Compare the false negative alerts from both methods - Explore the temporal and quantitative relation between fetal lactate metabolism and ST interval changes of the fetal ECG ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04779294
Study type Observational
Source Oslo University Hospital
Contact
Status Completed
Phase
Start date September 1, 2018
Completion date October 31, 2023

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