Coenzyme Q10 in Pediatric Community-Acquired Pneumonia

NCT ID: NCT07317440

Last Updated: 2026-01-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

120 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-12-31

Study Completion Date

2026-12-31

Brief Summary

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The aim of this work is to assess the benefit of coenzyme Q10 supplementation, in addition to standard antibiotic and other supportive therapy, in the management of hospitalized children with community acquired pneumonia

Detailed Description

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Conditions

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Community Acquired Pneumonia

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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60 children with community acquired pneumonia will receive oral coenzymeQ10

Group Type EXPERIMENTAL

oral coenzymeQ10

Intervention Type DRUG

60 children with community acquired pneumonia will receive oral coenzymeQ10 in capsule form at a dose of 100-200 mg/kg/day, as adjunct therapy to the usual pneumonia treatment till the recovery of the disease.

60 children with community acquired pneumonia with the standard pneumonia treatment.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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oral coenzymeQ10

60 children with community acquired pneumonia will receive oral coenzymeQ10 in capsule form at a dose of 100-200 mg/kg/day, as adjunct therapy to the usual pneumonia treatment till the recovery of the disease.

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* All children aged 2 months -18 years with community acquired pneumonia diagnosed by signs and symptoms of CAP including; chest pain, dyspnea, tachypnea, or abnormal auscultatory findings plus focal findings on chest x ray indicating community acquired pneumonia

Exclusion Criteria

* Children with immunodeficiency, chronic lung disease, malignancy, congenital lung anomalies, underlying disorder impacting respiration i.e. genetic, metabolic, neuromuscular disorders, children with CHD affecting the pulmonary blood flow.
Minimum Eligible Age

2 Months

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Tanta University

OTHER

Sponsor Role lead

Responsible Party

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Rehab Zaki Elmeazawy

Lecturer of pediatrics

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Tanta University

Tanta, Gharbia Governorate, Egypt

Site Status

Countries

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Egypt

Central Contacts

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Ahmed Elniny Lecturer of Pediatrics, MD

Role: CONTACT

01002219783

Facility Contacts

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Rehab Zaki Elmeazawy

Role: primary

01004815280

Role: backup

Other Identifiers

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36264PR1169/3/25

Identifier Type: -

Identifier Source: org_study_id

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