A clinical trial to study use of fetal scalp stimulation test in management of fetal distress during labour

Not Applicable

Completed

• Registration Number: CTRI/2009/091/000030
• Lead Sponsor: nill

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 200

Inclusion Criteria

1.Women with singleton pregnancy >37 weeks periods of gestation, cephalic presentation in active labour.
2.Non- Reassuring FHR patterns
&#9679; FHR<110 bpm
&#9679; FHR>160 bpm
&#9679; Decelerations or postcontraction drops

Exclusion Criteria

1.Gross congenital anomaly of the baby diagnosed in ante-natal or neonatal period.
2.Indication for immediate cesarean section at the time of recruitment.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1.Umbilical artery pH and base deficit at birth.<br>2.Neonatal morbidity in terms of <br>a.Apgar score &lt;5 &amp; 7 at min. 1 and 5<br>b.Nursery admissions<br>c.Hypoxic ischemic encephalopathy<br>3.Caesarean section rate for fetal distress. <br>Timepoint:

Secondary Outcome Measures

Name	Time	Method
1.Overall (all causes)operative delivery rates. <br>2.Operative delivery rates for fetal distress.<br>3.Neonatal mortality.<br>4.Maternal morbidity like fever. <br>Timepoint: