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Study of easy to use pregnancy monitoring device

Feasibility, accuracy & validation study of the fetal heart rate (using fetal ECG) and uterine contraction (using uterine EMG) monitoring device during intra-partum period and to study the feasibility of prediction of fetal distress via pattern analysis of aforementioned parameters

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2018/11/016464
Enrollment
2016
Registered
2018-11-28
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: O80- Encounter for full-term uncomplicated delivery

Interventions

Intervention1: NA: NA Control Intervention1: NA: NA

Sponsors

Janitri Innovations Private Limited
Lead Sponsor

Eligibility

Inclusion criteria

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

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
To determine the feasibility of prediction of fetal distress by pattern analysis of acquired fetal heart rate and uterine contraction dataTimepoint: April 2019—

Countries

India

Contacts

Public ContactArun Agarwal

Janitri Innovations Private Limited

arun@janitri.in9952279155

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026