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Monitoring of High Risk Pregnancy patients based on Ultrasound Doppler

Completed
Conditions
Pregnancy
Registration Number
CTRI/2010/091/000175
Lead Sponsor
Philips
Brief Summary

Pregnancy Monitoring Study is intended to collect clinical data for training and testing algorithms. We will be using only currently available non-invasive devices for this study (Ultrasound-Doppler) at 5 centres in India.

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
200
Inclusion Criteria

Should be older than or atleast 18 years oldSingleton or Multiple Pregnancy Pregnancy should be normal, or with one or more of the following past history or complications (like maternal diabetes,renal disease,heart disease,Thyroid and other hormonal disorders, coagulation disorder,hypertension,IUGR,gestational diabetes).

Exclusion Criteria

Pregnancy less than 12 weeks of gestationPresence of a complication of pregnancy other than the ones cited in the inclusion criteriaPresence of fetal Malformation.

Study & Design

Study Type
Not specified
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To collect clinical data for training and testing algorithms
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (7)

Bangalore Fetal Medicine, C.J. D' Souza Road

🇮🇳

Bangalore, KARNATAKA, India

Bharat Scans Pvt Ltd

🇮🇳

Chennai, TAMIL NADU, India

C- l5 MRI lmaging & Diagnostic Research Centre

🇮🇳

Delhi, DELHI, India

Dr. Jolly?s Diagnostic Centre

🇮🇳

Delhi, DELHI, India

Health and Research Centre

🇮🇳

College, India

Mediscan

🇮🇳

Chennai, TAMIL NADU, India

Pristine Hospital

🇮🇳

Bangalore, KARNATAKA, India

Bangalore Fetal Medicine, C.J. D' Souza Road
🇮🇳Bangalore, KARNATAKA, India
Dr. Prathima Radhakrishnan
Principal investigator

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