Skip to content

Effectiveness of Zingiber officinale to reduce inflammation in community acquired pneumonia

Effectiveness of Zingiber officinale to reduce inflammation markers and the length of stay of patients with community acquired pneumonia patients: A clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20230414002
Enrollment
30
Registered
2023-04-14
Start date
2022-07-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

met the diagnostic criteria of CAP confirmed by pneumonia symptoms such as cough, change/purulence of sputum color, fever, or breathlessness had pneumonia sign by chest X-ray (infiltrate of pneumonia). community acquired pneumonia Zingiber officinale var rubrum inflammatory marker length of hospitalization

Interventions

In treatment group, the patients received oral Z. officinale capsule 300 mg daily for five days as well as CAP standard therapy. ,In the control group, the patient received CAP standard therapy
Experimental Drug,No Intervention Drug

Sponsors

Indonesia Non (state budget) APBN funds of research institutions and community service
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. met the diagnostic criteria of CAP 2. confirmed by pneumonia symptoms such as cough, change/purulence of sputum color, fever, or breathlessness 3. had pneumonia sign by chest X-ray (infiltrate of pneumonia).

Exclusion criteria

Exclusion criteria: 1. severe CAP 2. having cardiopulmonary failure 3. physical disfunction who could not complete the study 4. patients with mental or communication disorder were excluded

Design outcomes

Primary

MeasureTime frame
IL-6 5 days after intervention IL-6 Human ELISA kit (DE2132) quantitative assay,PCT 5 days after intervention PCT Human ELISA kit (E-EL-H1492) quantitative assay,NLR 5 days after intervention leukocyte diffcount examination by using a blood smear and be counted manually (Neubauer)

Secondary

MeasureTime frame
Length of stay 5 days after intervention Total days from admission until discharge date

Countries

Indonesia

Contacts

Public ContactBrigitta Devi Hapsari

Medical Faculty Sebelas Maret University

brigitta.anindita@staff.uns.ac.id85647328553

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026