New Sensors for Monitoring Fetal Health in Late Pregnancy
Validation of Sensors for Long-term Non-Invasive Fetal Monitoring
Recruiting
N/A
Interventional Study
Fetal Distress With Antenatal Problem
Fetal Growth Retardation
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 16 – 50
- Sex
- Female
- Study type
- Interventional
- Purpose
- Other
- Participants needed
- 69 (estimated)
- Sponsor
- University of Manchester · Other
Who this trial is looking for
This trial is looking for women in late pregnancy to test new sensors that measure the heartbeats and movements of the baby. Participants will help us see how well these sensors work compared to current methods.
Are You a Good Fit for This Trial?
You may be able to join if
- I have a singleton pregnancy after 28 weeks.
- I have an estimated fetal weight between the 10th and 90th percentiles.
- I am 16 years or older.
You may not be able to join if
- I have fetal anomalies.
- I am pregnant with more than one baby.
- I have evidence of fetal growth restriction.
- I cannot speak or understand fluent English.
- I am under 16 years old.
Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
Check Your Eligibility
About This Trial
A multidisciplinary team of a doctor and engineers have developed a new sensor that will be able to detect mothers' and babies' heartbeat and babies movements in late pregnancy. This sensor can be placed in contact with the mothers' skin over the pregnant uterus without having to be stuck down. We anticipate that this sensor would allow us to monitor babies for longer periods of time which might h…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Participants will be included if they have a non-anomalous singleton pregnancy after 28 weeks' gestation with an estimated fetal weight \>10th centile \< 90th centile. Participants will be 16 years or over in order that they can give independent consent.
Exclusion Criteria:
…
Contacts