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The predictive value of rectus femoris cross-sectional area for hypotension during airway intervention under general anesthesia: A prospective observational cohort study

The predictive value of rectus femoris cross-sectional area for hypotension during airway intervention under general anesthesia: A prospective observational cohort study

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600121622
Enrollment
Unknown
Registered
2026-04-01
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Perioperative hypotension

Interventions

Case group:None

Sponsors

Emergency General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age >=18 years; 2.The American Society of Anesthesiologists (ASA) physical condition is classified as grade II-IV; 3.Rigid bronchoscopic interventional therapy under general anesthesia was planned; 4.Able to understand research and sign voluntary informed consent;

Exclusion criteria

Exclusion criteria: 1.Preoperative hemodynamics were unstable (EG, shock, uncontrolled decompensated heart failure) . 2.Poor preoperative blood pressure control: systolic blood pressure >=180mmHg or diastolic blood pressure >=110mmHg; or systolic blood pressure 1 month); 7.Presence of severe neuromuscular disorders (EG, myasthenia gravis, amyotrophic lateral sclerosis, etc.) or prolonged bed rest (> 14 days) for other reasons; 8.Severe trauma, deformities, surgical incisions, skin infections, or extensive rashes on both thighs preclude ultrasound measurements; 9.Patients had severe hepatorenal dysfunction (such as Child-Pugh grade C, or estimated glomerular filtration rate EGFR < 15 mL/min/1.73 m2) or severe cardiac dysfunction (NYHA grade IV); 10.The investigators judged that there were any other circumstances that might interfere with the study's assessment or increase the subject's risk;

Design outcomes

Primary

MeasureTime frame
RF-CSA measurements;Intraoperative hypotension (IOH);

Countries

China

Contacts

Public ContactXu Jing

Emergency General Hospital

xujingsunny82@sina.com+86 10 87935413

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026