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Reason Evaluation of Initial Treatment Failure in Patients With CAP

Reason Evaluation of Initial Treatment Failure in Patients With Community Acquired Pneumonia

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03280004
Acronym
RECAP
Enrollment
314
Registered
2017-09-12
Start date
2017-11-20
Completion date
2019-11-30
Last updated
2019-04-29

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

Conditions

Community-acquired Pneumonia

Brief summary

This research is to evaluate the effect of different antibiotics (Moxifloxacin Hydrochloride and Sodium Chloride Injection vs. β-lactam antibiotics for injection +/- Azithromycin for Injection) on the early deterioration or progression (\<72 h of treatment) of community acquired pneumonia and to study the effect of the early deterioration or progression on the prognosis of community acquired pneumonia.

Interventions

DRUGMoxifloxacin Hydrochloride and Sodium Chloride Injection

Moxifloxacin group will be given Moxifloxacin Hydrochloride and Sodium Chloride Injection and β-lactams group will be given β-lactam antibiotics for injection +/- Azithromycin for Injection.

Sponsors

Peking Union Medical College Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Age\>=18y. 2. Diagnosed with CAP. 3. Need hospitalization. 4. Receive Moxifloxacin Hydrochloride and Sodium Chloride Injection or β-lactam antibiotics for injection +/- Azithromycin for Injection as initial treatment. 5. Signed informed consent form.

Exclusion criteria

Patients who meet any of the following criteria will not be included in the study: 1. Pneumonia is aquired more than 48h after admission or the patient was admitted to hospital within 30 days prior to admission. 2. Start antibiotic treatment before admission. 3. Gestational period or suckling period. 4. Admitted to ICU. 5. Immunocompromised patients. 6. Pneumonia is the terminal event of a serious disease. 7. Tuberculosis, lung cancer, non-infectious interstitial lung disease, pulmonary edema, atelectasis, pulmonary embolism, pulmanory eosinophilia, pulmonary vasculitis. 8. Allergic to the antibiotics of the study.

Design outcomes

Primary

MeasureTime frame
early deterioration or progression rate3 days

Countries

China

Contacts

Primary ContactJun Xu, MD
xujunfree@126.com010-69159142

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026