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Exploratory study on the treatment of orthopedic infection with coriomycin tablets

Exploratory study on the treatment of orthopedic infection with coriomycin tablets

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100047037
Enrollment
Unknown
Registered
2021-06-07
Start date
2021-08-01
Completion date
Unknown
Last updated
2022-01-18

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

Conditions

orthopedic infection

Interventions

Experimental group1:Tazocin and Colimycin
Control group1:Tazocin
Experimental group2:Tazocin and Colimycin and Mepem
Control group2:Tazocin and Mepem

Sponsors

Shanghai Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. The pathogen was cro; 2. Cro: sputum culture for carbapenem resistant Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa and Acinetobacter baumannii; 3. The age is more than 18 years old (including the boundary value), regardless of gender; 4. Informed consent has been signed by the subject or legal representative.

Exclusion criteria

Exclusion criteria: 1. Patients who are known to be allergic to the study drug or active ingredients; 2. Patients with bloodstream infection; 3. Liver dysfunction (ALT and / or AST) 5 times of the upper limit of normal value, and / or 1.5 times higher than the upper limit of normal value of total bilirubin, or child Pugh score C); 4. Patients with severe renal injury (creatinine clearance rate < 30ml / min); 5. Clinically serious gastrointestinal dysfunction may affect the intake, transportation or absorption of the study drugs, such as uncontrollable nausea or vomiting, history of extensive gastrointestinal resection, recurrent diarrhea without cure, Crohn's disease, ulcerative colitis; 6. Combined use of warfarin, anticonvulsant drugs, statins, cisapride, immunosuppressant drugs, digoxin and ergot drugs 7. Combined use of macrolides, aminoglycosides, tetracyclines, linezolid and other drugs to inhibit the protein synthesis of pathogenic microorganisms; 8. Those who have participated in other clinical trials within 4 weeks before screening; 9. Pregnant women, lactating women and subjects (including male subjects) have pregnancy plans (including sperm donation and egg donation plans) or are unable to take effective contraceptive measures in the next six months; 10. Other circumstances considered unsuitable by the researcher.

Design outcomes

Primary

MeasureTime frame
infection control;

Countries

China

Contacts

Public ContactYang Qingcheng

Shanghai Sixth People's Hospital

tjyqc@163.com+86 18930177328

Outcome results

None listed

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