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Clarithromycin in Post Covid 19 parenchymal organizing pneumonia

Clarithromycin in post Covid parenchymal organizing pneumonia - an open labelled randomized control trial - PCOVID

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/11/029305
Enrollment
120
Registered
2020-11-24
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: J840- Alveolar and parieto-alveolar conditions Health Condition 2: J128- Other viral pneumonia

Interventions

Intervention1: Oral Clarithromycin 500 mg PO one tablet BiD for three months: Oral Clarithromycin 500 mg PO one tablet BiD for three months Intervention2: Oral Clarithromycin 250 mg PO one tablet BiD

Sponsors

SELF DrIrfan Ismail Ayub
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. All patients diagnosed with COVID 19 based on positive result on SARS-CoV2 RT-PCR or CBNAAT from nasopharyngeal or oropharyngeal swab or secretions. 2. More than two weeks, but less than six weeks have lapsed after the above diagnostic positive result. 3. A repeat nasopharyngeal or oropharyngeal swab test (either SARS-CoV2 RT-PCR or CBNAAT) performed at two weeks or later, after earlier positive result, is now negative. 4. CT scan of thorax performed after two weeks and less than six weeks after the first positive result, shows features of organizing pneumonia. Organizing pneumonia on CT scan of thorax is diagnosed when, one or more of the following features are identified on the CT scan images of thorax: 1.Unilateral or bilateral basal subpleural lobar, segmental or perilobular consolidation 2.Halo sign 3.Reverse halo sign or atoll sign 4.Target sign or bulls-eye sign or double halo sign

Exclusion criteria

Exclusion criteria: 1.Patient is unwilling to provide consent 2.Patients with preexisting parenchymal or interstitial lung disease

Design outcomes

Primary

MeasureTime frame
Percentage of patients with complete resolution of lung findings at third month of follow up.Timepoint: Three months of follow up

Secondary

MeasureTime frame
Secondary objective includes percentage of patients with more than 50% reduction in the CT severity score at three months, side effect and tolerance profile of patients in the Clarithromycin arm.Timepoint: Third month of follow up. However, every two weeks, a telephone consultation will be performed to assess side effects and symptom profile and drug compliance

Countries

India

Contacts

Public ContactIrfan Ismail Ayub

Sri Ramachandra Institute of Higher Education and Research

irfanismailayub@gmail.com9884282400

Outcome results

None listed

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