CTRI/2024/08/072499
Not yet recruiting
Phase 2
Evaluation of efficacy and safety of adjuvant Pentoxifylline therapy in adults with community acquired pneumonia: An Open label, Randomized-controlled trial. - NI
SARANDEV A T V0 sites0 target enrollmentTBD
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Health Condition 1: J189- Pneumonia, unspecified organism
- Sponsor
- SARANDEV A T V
- Status
- Not yet recruiting
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\)At least one acute clinical sign compatible with pneumonia (dyspnea, cough, purulent sputum, crackles)
- •2\)Infiltrate on chest X\-ray or CT scan suggestive of pneumonia
- •3\)Diagnosis of CAP at or during the 48 hours post\-hospital admission.
- •4\)Informed consent signed by the patient, his/her legally authorized representative.
Exclusion Criteria
- •1\)Patient on invasive mechanical ventilation.
- •2\)Patients with creatinine clearance less than 30 ml per minute
- •3\)Patient on vasopressors at the time of inclusion
- •4\)Any contraindications to the study drug
- •5\)Patient requiring corticosteroids (except for nebulized corticosteroids) for any reason.
- •6\)Patient treated with antibiotics for more than 7 days prior to admission.
- •7\)Suspicion of aspiration or heath care associated pneumonia.
- •8\)Active tuberculosis
- •9\)On immunosuppressive therapy or malignancy
- •10\)Pregnancy or lactating women
Outcomes
Primary Outcomes
Not specified
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