FRI a Method of Reading Cardiotocography (CTG) in Labor

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
AgeNot listed
SponsorFondazione Policlinico Universitario Agostino Gemelli IRCCS

About this trial

The objective of the study is to investigate the FRI's ability to identify cases requiring urgent intervention which will present an adverse perinatal outcome (respiratory acidosis, metabolic acidosis, Apgar index, etc.) compared to the classical interpretation of CTG.

Patients whose CTG in labor will be considered non-reassuring will be enrolled and randomized into two groups. The "Fetal Reserve Index" algorithm will be applied to the first group of patients.

The second group of patients will, however, be managed according to the usual protocols internal management.

Eligibility criteria

Qualifiers

Women in the active phase of labor who presented when they entered the room I delivered a negative admission test (i.e. a normoreactive CTG according to ACOG) and that subsequently present during labor a diagnosis of category II CTG

Single term pregnancy

Signature of informed consent

Disqualifiers

Failure to sign the informed consent

Previous caesarean section (TOLAC)

Twin pregnancy

Gestational age <37 weeks

Trial design

Treatments tested in this trial

  • Interpretation of the CTG using FRI score
  • Classic interpretation of the CTG

Treatment groups

290 Participants
are divided into 2 treatment groups