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Evaluation of modified end-expiratory occlusion test in the elderly receiving perioperative lung protective ventilation

Evaluation of modified end-expiratory occlusion test in the elderly receiving perioperative lung protective ventilation

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100049587
Enrollment
Unknown
Registered
2021-08-05
Start date
2020-06-26
Completion date
Unknown
Last updated
2022-04-19

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

Conditions

Fluid responsiveness

Interventions

Gold Standard:Changes in SV induced by VE(250mL saline 0.9% given over 10minutes)test.
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Sponsors

Shanghai Fifth People's Hospital, Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 91 Years

Inclusion criteria

Inclusion criteria: 1. aged > 65 years; 2. ASA-PS 1 to 3; 3. requiring invasive arterial monitoring; 4. in the supine position.

Exclusion criteria

Exclusion criteria: 1. severe lung disease before anesthesia; 2. contraindications for volume expansion; 3. arrhythmia; 4. cardiac insufficiency; 5. body mass index >30 or <15 kg/m2; 6. use of vasopressors or inotropes before and during anesthesia.

Design outcomes

Primary

MeasureTime frame
stroke volume index;—

Countries

China

Contacts

Public ContactJun Tang, Han Chen

Shanghai Fifth People's Hospital, Fudan University

mdtangj@sina.com+86 18930819727

Outcome results

None listed

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