Actively Recruiting

All Genders
ID06711562

Model-informed Individualized Treatment of Anti-infective Drugs in Patients With Osteoarticular Infections

Led by Shandong University · Updated on 2024-12-02

300

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating how to optimize personalized treatment of anti-infective drugs for people with osteoarticular infections by studying drug levels in the blood and tissues. This observational study aims to better understand how these drugs behave in the body using population pharmacokinetics, which can help guide dosing decisions. Participants will receive anti-infective drugs following traditional clinical dosing without additional interventions. The study mainly observes and collects data on drug clearance and distribution over about 30 days. During the study, participants will have their drug exposure measured through blood or tissue samples. Researchers will also monitor markers like erythrocyte sedimentation rate and record any adverse events. The study lasts approximately 30 days to collect all relevant data for analysis.

CONDITIONS

Brief Title

Model-informed Individualized Treatment of Anti-infective Drugs

Who Can Participate

All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients with suspected or confirmed osteoarticular infections who are receiving anti-infective drug therapy
Not Eligible

You will not qualify if you...

  • Pregnant or breastfeeding women
  • Any other factors that researchers consider unsuitable for participation

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Approximately 30 days

Participants receive anti-infective drugs according to traditional clinical dosing regimens without additional interventions.

Visits scheduled as part of routine care

Long-term Monitoring

Duration - Up to 30 days

Participants are monitored for drug clearance, volume of distribution, and safety outcomes during and after treatment.

Visits scheduled as part of routine care

Trial Site Locations

Total: 1 location

1

Shandong Public Health Clinical Center

Jinan, China

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Research Team

W

Wei Zhao, Ph.D

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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