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Intraoperative and postoperative effects of sarcopenia on patients undergoing general surgery

Intraoperative and postoperative effects of sarcopenia on patients undergoing general surgery

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400091621
Enrollment
Unknown
Registered
2024-10-31
Start date
2024-11-01
Completion date
Unknown
Last updated
2024-11-04

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

Conditions

Sarcopenia

Interventions

Sarcopenia group:None

Sponsors

General Hospital Of Eastern Theater Command
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Subjects are voluntary and sign the informed consent form for this trial 2. The patient is aged 18-65 years 3. Patients undergoing surgical treatment for general surgery 4. ASA grade 2-3

Exclusion criteria

Exclusion criteria: 1. Allergic to the anesthetic used 2.Hepatic and renal insufficiency or neurological disease 3.Uncontrolled high blood pressure 4.Patients diagnosed with non-general surgical diseases 5.Patients with other preoperative causes of muscle weakness (injury, fracture, stroke, etc.)

Design outcomes

Primary

MeasureTime frame
Intraoperative anesthetic drug dosage;The number of intraoperative adverse events;Baseline mean arterial pressure;Baseline heart rate;Composite complication index at 30 days after surgery;

Secondary

MeasureTime frame
Minimum mean arterial pressure;

Countries

China

Contacts

Public ContactQing Ji

General Hospital Of Eastern Theater Command

qing_ji@nju.edu.cn+86 139 1391 5619

Outcome results

None listed

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