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Fetal Scalp Stimulation Versus Fetal Blood Sampling in Labour

Fetal Scalp Stimulation (FSS) Versus Fetal Blood Sampling (FBS) to Assess Fetal Wellbeing in Labour - a Multi-centre Randomised Controlled Trial.

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05306756
Acronym
FIRSST
Enrollment
40
Registered
2022-04-01
Start date
2022-05-10
Completion date
2023-08-31
Last updated
2024-02-20

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

Conditions

Intrapartum Fetal Distress

Keywords

randomised controlled trial, fetal blood sampling, fetal scalp stimulation, cardiotocography, caesarean section

Brief summary

Pregnant women have routine monitoring of the baby's heart rate when in labour. Women with complicated pregnancies require continuous monitoring using an electronic recorder called a CTG. The CTG produces a paper based recording which is interpreted by the midwife as showing normal, suspicious or abnormal features of the baby's heart rate. Babies quite commonly demonstrate abnormal features from time to time during the course of labour. In some cases the abnormal features are of sufficient concern to warrant delivery by emergency caesarean section. In most of these cases the baby is born in good condition and the question arises whether the caesarean section was unnecessary. In order to reduce the chance of an unnecessary caesarean section additional second-line tests can be offered. One such test is where a small drop of blood is taken from the baby's scalp. This test involves an internal examination with an instrument to visualise the baby's head and a small scratch to the baby's scalp. The blood is tested for acid which is an indicator of whether or not the baby is receiving enough oxygen. The test is called a fetal blood sample or FBS. An alternative test is where the doctor or midwife performs a vaginal examination with two fingers and gently rubs the baby's scalp in an attempt to cause an increase in the baby's heart rate. This is a healthy response suggesting that the baby is receiving enough oxygen. The test is called digital fetal scalp stimulation or dFSS. These two second-line tests have never been compared in a properly conducted head-to-head comparison. This study aims to compare dFSS and FBS in a large clinical trial completed within four of Ireland's largest maternity hospitals. This trial will generate important evidence of direct relevance to clinical care and patient outcomes.

Detailed description

Continuous electronic fetal heart rate recording with cardiotocography (CTG) is a standard approach to monitoring fetal wellbeing in labour and is recommended for high-risk pregnancies. The aim is to identify fetal compromise early and intervene in order to reduce serious adverse events such as cerebral palsy and perinatal death. CTG abnormalities are relatively common and can lead to the decision to deliver by emergency caesarean section. In most cases the fetus is subsequently found to have been compensating for the stress of labour and is not actually compromised. Fetal blood sampling (FBS) is a second-line invasive test that provides information on the acid-base status of the fetus, reflecting hypoxia. It is used to provide either reassurance that labour can continue, or more objective evidence that delivery needs to be expedited. Clinical guidelines in the United Kingdom and Ireland have treated FBS as a gold standard test. Recent studies have questioned the validity and reliability of FBS, and also the logistic challenges of achieving a result in a timely manner. Fetal scalp stimulation (dFSS) by digital rubbing is an alternative less invasive test of fetal wellbeing in labour and is recommended in preference to FBS in US guidelines. This research aims to compare digital FSS and FBS in women with term singleton pregnancies and an abnormal intrapartum CTG, where additional information on fetal wellbeing is required. A multi-centre randomised controlled trial will be conducted. The clinical outcomes of interest will include caesarean section, assisted vaginal birth, low Apgar scores, cord blood acidosis, and admission to the neonatal unit. This trial will generate important evidence of direct relevance to clinical care and patient outcomes.

Interventions

DIAGNOSTIC_TESTFetal Blood Sampling (FBS)

Vaginal examination, insert amnioscope through cervix, visualise fetal scalp, clean fetal scalp, apply ethyl chloride spray, wipe scalp with petroleum gel, small scalp scratch with sharp instrument, collect sample in heparinised capillary tube, analyse sample.

DIAGNOSTIC_TESTdigital Fetal Scalp Stimulation (dFSS)

Vaginal examination, insert one or two fingers through cervix onto fetal scalp, rub fetal scalp digitally for approximately 30-60 seconds, withdraw fingers and observe CTG for 5-10 minutes.

Sponsors

University College Cork
CollaboratorOTHER
University of Limerick
CollaboratorOTHER
Royal College of Surgeons, Ireland
CollaboratorOTHER
National University of Ireland, Galway, Ireland
CollaboratorOTHER
Health Research Board, Ireland
CollaboratorOTHER
Health Research Board - Trials Methodology Research Network
CollaboratorOTHER
University of Dublin, Trinity College
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
DOUBLE (Investigator, Outcomes Assessor)

Masking description

The primary and perinatal secondary outcomes will be recorded from the computerised delivery record without knowledge of the allocation. The principal investigator will play no role in the care of the patient or assessment of outcomes.

Intervention model description

Patients in labor with CTG abnormalities that warrant second-line testing of fetal wellbeing - randomized to digital fetal scalp stimulation (dFSS) versus fetal blood sampling (FBS)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Nulliparous women * Singleton pregnancy * Cephalic presentation * Gestational age 37+0 weeks or greater * Abnormal CTG that requires second-line testing (FBS or dFSS)

Exclusion criteria

* Contraindication to FBS * Limited understanding of English * At the discretion of the responsible obstetrician in cases where there is urgency

Design outcomes

Primary

MeasureTime frameDescription
Caesarean section (CS)at birthAll caesarean sections will be in labour in the context of an abnormal CTG

Secondary

MeasureTime frameDescription
Therapeutic hypothermiaindicated within 6 hours of birthtreatment for encephalopathy
Caesarean section , primary indication fetal concernsat birthabnormal CTG, or meconium, or low pH on FBS
Caesarean section, primary indication poor progressat birthPoor progress in first or second stage of labour
Caesarean section, failed attempt at assisted vaginal birthat birthFailed vacuum or forceps in second stage of labour
Assisted vaginal birth (AVB) (all cases)at birthVacuum or forceps or sequential (vacuum and forceps)
Assisted vaginal birth, primary indication fetal concernsat birthabnormal CTG, or meconium, or low pH on FBS
Assisted vaginal birth, primary indication poor progressat birthPoor progress in second stage of labour
Spontaneous Vaginal Birth (SVB)at birthunassisted birth
Decision Delivery Interval (DDI) for emergency CS >30 minutesduring labour up until time of birthDecision delivery interval prolonged
Decision Delivery Interval (DDI) for AVB >15 minutesduring labour up until time of birthDecision delivery interval prolonged
Perinatal deathup to 7 days of ageintrapartum or early neonatal death
Late perinatal death8-28 days of lifeafter 7 days up to 28 days of age
Neonatal encephalopathy (as defined by authors)from birth up until 28 daysprotocol definition
pH umbilical artery <7.00 or Base Excess artery <-12.0immediately after birtharterial cord blood acidosis
Admission to neonatal unit (NNU)from birth up until 28 daysadmission all causes
Abnormal neurological examination prior to dischargeat time of hospital discharge, assessed up to 28 days after birthclinical assessment recording abnormal findings - tone, reflexes, gag
FBS related injury/complication to baby (as reported on neonatal examination)at birth or with first 7 days of lifetraumatic injury or abnormal bleeding
Major obstetric haemorrhage >1000mLup to 24 hours after birthpostpartum haemorrhage
Obstetric Anal Sphincter Injury (OASI - all degrees)at birthinjury either spontaneous or with episiotomy
Referral to perinatal mental health servicesfrom birth up to six weeks after birthpsychological symptoms warranting referral
Maternal acceptability of procedure (defined by questionnaire)from birth up to 7 days after birthacceptability
Number of second-line tests (dFSS or FBS)during labour up until birtheach event (rather than samples taken)
Number of inconclusive/uninterpretable dFSS proceduresduring labour up until birthno clear acceleration or variability borderline
Number of failed FBS proceduresduring labour up until birthno sample or reliable result achieved
Apgar score at 5 minutes <7age 5 minuteslow Apgar score at 5 minutes

Countries

Ireland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026