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Evaluation of Efficacy and Safety Parameters of Different Antibiotics Regimens for Management of Empyema

F

Fayoum University

Status

Enrolling

Conditions

Empyema, Pleural

Treatments

Drug: Moxifloxacin + meronam
Drug: Levofloxacin + cefipime
Drug: Levofloxacin + clindamycin

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

To evaluate the impact of using different antibiotic regimens including single and combined agents as the empirical therapy and evaluate the clinical outcomes regarding safety, efficacy, and pharmacodynamics parameters.

Enrollment

90 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Confirmed Diagnosis of Empyema: Patients with a clinical and radiological diagnosis of

Exclusion criteria

1 - Hypersensitivity or Allergy to the selected antibiotic: Patients with a known history of hypersensitivity or allergic reactions to used antibiotics.

2- Pregnancy and Lactation

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

90 participants in 3 patient groups

Patient with empyema
Other group
Description:
Tavanic (levofloxacin )and dalacin (clindamycin)
Treatment:
Drug: Levofloxacin + cefipime
Empyema patient
Other group
Description:
Tavanic (levofloxacin) and cefipime
Treatment:
Drug: Levofloxacin + clindamycin
patient has lung empyema
Other group
Description:
Moxiflox (moxifloxacin) and meronem
Treatment:
Drug: Moxifloxacin + meronam

Trial contacts and locations

1

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Central trial contact

Abdelrahman Ahmed Mohamed, Teaching Assistant; Marwa Kamal Tolba, Assistant professor

Data sourced from clinicaltrials.gov

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