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A prospective observational study based on real-time transdermal glomerular filtration rate monitoring to evaluate the pharmacokinetic characteristics of vancomycin and the accuracy of dose prediction in septic patients.

A prospective observational study based on real-time transdermal glomerular filtration rate monitoring to evaluate the pharmacokinetic characteristics of vancomycin and the accuracy of dose prediction in septic patients.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600125721
Enrollment
Unknown
Registered
2026-05-29
Start date
2026-05-29
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Sepsis

Interventions

Sponsors

Ruijin Hospital, Shanghai Jiao Tong University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Age >=18 years old; 2.ICU patients diagnosed with sepsis or septic shock; 3.A clinical decision was made to treat with vancomycin, and the expected treatment duration is =3 days. 4.Informed consent form has been signed.

Exclusion criteria

Exclusion criteria: 1.Allergy to fluorescent tracers (pyrazine derivatives) or related components. 2.History of photosensitive diseases; 3.Pregnant or breastfeeding women; 4.The skin at the monitoring site has large areas of damage or infection. 5.The researchers determined that participation was not suitable.

Design outcomes

Primary

MeasureTime frame
Compare the accuracy of tGFR and traditional eGFR in predicting the steady-state trough concentration of vancomycin in patients with sepsis;

Secondary

MeasureTime frame
The performance of tGFR in identifying enhanced renal clearance (ARC);The correlation between tGFR and individual vancomycin clearance rate;

Countries

China

Contacts

Public ContactHongping Qu

Ruijin Hospital, Shanghai Jiao Tong University School of Medicine

hongpingqu0412@hotmail.com+86 21 6437 0045

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026