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International Fetal Anesthesia Database

International Fetal Anesthesia Database

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02591745
Acronym
iFAD
Enrollment
2000
Registered
2015-10-30
Start date
2015-01-31
Completion date
2030-01-31
Last updated
2025-02-19

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

Conditions

Determination of Neurological Outcomes

Keywords

Fetal, Anesthesia

Brief summary

This registry aims to gather anesthetic medications administered to fetuses directly as well as those administered via the mother during fetal intervention procedures. The goal is to assesss short and medium term outcomes as well as long term outcomes of these babies whao have received medication in utero. The long term outcomes will include but are not limited to neurodevelopmental outcomes.

Detailed description

Advances in technology have allowed for an increase in procedures performed on the fetus in utero; these procedures involve the administration of different anesthetics (sedative- hypnotic agents and or volatile agents) to the mother and sometimes directly to the fetus in order for succesful completion of the procedure. Very few instiututions in the world perform these procedures in any significant number. The establishment of this database will serve to consolidate information regarding anesthetic drugs administered for these procedures, thereby helping to establish best practice guidelines, determine medium and short term outcomes or complications and also facilitate long term neurodevelopmental assessment of children that have undergone these procedures in utero with 5 and 10 year neurodevelopmental assessment.

Interventions

PROCEDUREFetal intervention

Type of fetal conditions requiring intervention and medications administered to fetuses undergoing varying types of fetal intervention will be documeted in this database.

Sponsors

Baylor College of Medicine
Lead SponsorOTHER
Children's Hospital Medical Center, Cincinnati
CollaboratorOTHER
Universitaire Ziekenhuizen KU Leuven
CollaboratorOTHER
The University of Texas Health Science Center, Houston
CollaboratorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

Pregnant women, fetuses and children

Exclusion criteria

Non-pregnant women

Design outcomes

Primary

MeasureTime frameDescription
Fetal complicationsPeri-operativeresuscitation efforts during surgery or peri-operative demise

Secondary

MeasureTime frame
Maternal hypotension or other maternal complicationsPeri-operative period

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026