Prospective evaluation of minimal invasive clinical parameters for perioperative fluid management in patients undergoing fetoscopic spina bifida repair

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00040612

Enrollment

Registered

2026-06-15

Start date

2026-06-18

Completion date

Unknown

Last updated

2026-08-03

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

Conditions

foetal open spinal dysraphism Q05

Interventions

Group 1: Pregnant women undergoing elective fetoscopic surgery in general anaethesia for foetal spina bifida Perioperativly (before, during and directly after surgery) as well as the following two day

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: patients undergoing prenatal foetal surgery for spina bifida

Exclusion criteria

Exclusion criteria: not needed

Design outcomes

Primary

Measure	Time frame
Incidence of maternal, especially pulmonary, complications within the day of surgery and the following two days collecting clinical routine data	—

Secondary

Measure	Time frame
Results of minimally invasive measurements (blood gas analysis, lung ultrasound and advanced haemodynamic monitoring without transpulmonary thermodilution)	—

Countries

Germany

Contacts

Public ContactStephanie Nolte

Universitätsklinikum Marburg, Philipps Universität Marburg

oppelts@med.uni-marburg.de+49 6421 58 69412

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Aug 10, 2026