Uterine contraction monitoring device during labor period

Feasibility, accuracy and validation study of the uterine contraction monitoring device using uterine electromyography (EMG) during intra-partum period

Status

Recruiting

Phases

Phase 1

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2017/02/007818

Enrollment

100

Registered

2017-02-08

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: null- Pregnant women during intra-partum period Health Condition 2: O099- Supervision of high risk pregnancy, unspecified

Interventions

Intervention1: NIL: NIL Intervention2: NIL: NIL Control Intervention1: NIL: NIL

Eligibility

Inclusion criteria

Inclusion criteria: The pregnant women who are in labor, admitted to labor ward and willing to participate in the study

Exclusion criteria

Exclusion criteria: The pregnant women who are in labor, admitted to labor ward and not willing to participate in the study

Design outcomes

Primary

Measure	Time frame
Feasibility of the surface electrodes for acquisition of the real time uterine contraction signal using EMG (electromyography) during intra-partum periodTimepoint: December 2017	—

Secondary

Measure	Time frame
Accuracy of the acquired uterine contraction signal with the Toco signalTimepoint: NIL	—

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