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Volatile compared with total intravenous anaesthesia in patients undergoing perventricular device closure of perimembranous ventricular septal defect:a randomized study

Volatile compared with total intravenous anaesthesia in patients undergoing perventricular device closure of perimembranous ventricular septal defect:a randomized study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-17012804
Enrollment
Unknown
Registered
2017-09-26
Start date
2017-09-28
Completion date
Unknown
Last updated
2017-10-02

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

Conditions

ventricular septal defect

Interventions

Group 1:total intravenous anaesthesia
Group 2:inhalation anaesthesia

Sponsors

Guangdong Provincial Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 18 Years

Inclusion criteria

Inclusion criteria: patients between the ages of 0-18 years, ASA I-III who were planed to undergo perventricular device closure of perimembranous ventricular septal defect.

Exclusion criteria

Exclusion criteria: Children with quality less than 2.5 kg; Emergency surgery; Severe heart and lung disease; Severe liver and renal insufficiency;

Design outcomes

Primary

MeasureTime frame
Plasma troponin concentration;—

Secondary

MeasureTime frame
blood gas analysis;lactic acid;blood glucose;—

Countries

China

Contacts

Public ContactGao Fengzhao

Guangdong Provincial Hospital of Chinese Medicine

zhaogaofeng_97@163.com+86 15920387021

Outcome results

None listed

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