Effects of treatment of patients with craniosynostosis on pre-and postoeprative complications

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00028283

Enrollment

100

Registered

2022-03-03

Start date

2015-01-01

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

Q75.0 T81.1

Interventions

Group 1: intraoperative volume therapy isotonic but hyperchloremic (until 2017) Group 2: intraoperative volume therapy isotonic, isochloremic and isoionic (since 2017)

Eligibility

Sex/Gender

All

Age

4 Months to 24 Months

Inclusion criteria

Inclusion criteria: all non syndromal infants with sagittal synosthosis undergoing linear craniectomy

Exclusion criteria

Exclusion criteria: patients that received no operative correction of their craniosynostosis or stopped treatment

Design outcomes

Primary

Measure	Time frame
postoperative serum chloride level	—

Secondary

Measure	Time frame
pH, serum potassium, serum sodium and serum calcium	—

Countries

Germany

Contacts

Public ContactCornelius Busch

Klinik für Anästhesiologie

cornelius.busch@med.uni-heidelberg.de06221 5636351

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026