Postoperative flumazenil administration following preanesthetic anxiolysis with benzodiazepines in children

Postoperative flumazenil administration following preanesthetic anxiolysis with benzodiazepines in children - FLUMI

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00038978

Enrollment

100

Registered

2026-02-09

Start date

2026-03-01

Completion date

Unknown

Last updated

2026-04-27

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

Conditions

Anesthesia in children

Interventions

Group 1: Retrospective, monocentric cohort analysis of patient records/files/anesthesia protocols with regard to dosage, route of administration, duration of administration, time of benzodiazepine adm

Eligibility

Sex/Gender

All

Age

No minimum to 17 Years

Inclusion criteria

Inclusion criteria: Patients under the age of 18 who underwent surgery involving anesthesia at the Pediatric Orthopedic Clinic and who received benzodiazepines for anxiolysis prior to surgery.

Exclusion criteria

Exclusion criteria: incomplete data recording

Design outcomes

Primary

Measure	Time frame
Change in physician behavior regarding the administration of benzodiazepines for preoperative anxiolysis over the three defined periods 10/2024-12/2024, 02/2025-04/2025, 06/2025-08/2025	—

Secondary

Measure	Time frame
1) Incidence of benzodiazepine-induced hangovers 2) Exploratory characteristics of patients with benzodiazepine-induced hangovers 3) Exploratory characteristics of patients after antagonization with flumazenil 4) Dosage regimen of flumazenil depending on medical responsibility	—

Countries

Germany

Contacts

Public ContactClemens Miller

Orthopädische Kinderklinik Aschau im Chiemgau

c.miller@kiz-chiemgau.de+49 8052 171 0

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: May 1, 2026