HFR Doppler CUS during inguinal hernia repair Changes in cerebral perfusion measured by high frequency Doppler cerebral ultrasonography during anesthesia for inguinal hernia repair

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON19965

Enrollment

Registered

2021-01-18

Start date

2021-02-01

Completion date

Unknown

Last updated

2024-02-28

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

Conditions

Inguinal Hernia repair

Interventions

Observational study

Eligibility

Inclusion criteria

Inclusion criteria: Children 0 to 1 year of age (born premature and a term) without major cardiovascular or pulmonary disease undergoing surgical correction of unilateral or bilateral inguinal hernia

Exclusion criteria

Exclusion criteria: • Absence or refusal of parental informed consent • Extreme preterm born (< 28 weeks) • Emergency surgery for incarcerated inguinal hernia • Major cardiovascular, pulmonary, renal, oncological disease • Genetic syndrome

Design outcomes

Primary

Measure	Time frame
To assess the effect of standard anesthetic procedures on cerebral blood flow measured with CBFV and HFR Doppler CUS during inguinal hernia repair.	—

Secondary

Measure	Time frame
To correlate CBFV and HFR Doppler CUS to routine monitoring techniques including heart rate, blood pressure, peripheral oxygen saturation, and regional cerebral oxygenation.	—

Contacts

Public ContactJurgen de Graaff

Erasmus MC

j.degraaff@erasmusmc.nl+31614184374

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)