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To compare a new fetal heart rate monitoring machine with routinely used machine during delivery of baby.

Not Applicable
Conditions
Health Condition 1: O68- Labor and delivery complicated byabnormality of fetal acid-base balance
Registration Number
CTRI/2024/04/065158
Lead Sponsor
Rahul Bhakat
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1. Women with singleton pregnancy.

2. Gestation more than or equal to 32 weeks.

3. Admission in labour ward with labour pains.

Exclusion Criteria

1. Presence of antenatally detected major fetal anomaly.

2. Intrauterine death.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1. Agreement between the two devices in detecting Fetal heart rate. <br/ ><br>2. Correlation coefficient between the two devices in detecting Fetal heart rate. <br/ ><br> <br/ ><br>Timepoint: Measurement of fetal heart rate for continuous 6 minutes during first and / or second stage of labour only once at enrollment. <br/ ><br> <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
5. APGAR at 1 and 5 minutes <br/ ><br>6. Degree of resuscitation requiredTimepoint: Neonates after delivery till resuscitation is required;Decision taken regarding delivery of fetusTimepoint: Measurement of fetal heart rate continuously for 6 minutes during first/ second stage of labour during delivery once at the time of enrollment.;Detection of abnormal fetal heart rate/ Fetal distressTimepoint: Fetal heart rate will be continuously measured for 6 minutes during first/ second stage of labour during delivery once.;Number of device adjustments requiredTimepoint: During continuos measurement of fetal heart rate for 6 minutes during first/ second stage of labour.;Patient/ provider device satisfactionTimepoint: During continuous measurement of fetal heart rate for 6 minutes during first/ second stage of labour once.
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