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Study of easy to use pregnancy monitoring device

Not Applicable
Conditions
Health Condition 1: O80- Encounter for full-term uncomplicated delivery
Registration Number
CTRI/2018/11/016464
Lead Sponsor
Janitri Innovations Private Limited
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

All women in active labor (3-10 centimeters cervical dilatation) and gestational age >34 weeks

Exclusion Criteria

A woman in active labor and does not provide an informed consent

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To determine the feasibility, accuracy & validation of the fetal heart rate (using fetal ECG) and uterine contraction (using uterine EMG) monitoring device.Timepoint: November 2018
Secondary Outcome Measures
NameTimeMethod
To determine the feasibility of prediction of fetal distress by pattern analysis of acquired fetal heart rate and uterine contraction dataTimepoint: April 2019
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