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Clinical Observation of the Efficacy of Maiwei Yangfei Decoction in Treating Fibrotic Interstitial Lung Disease of Qi-Yin Deficiency Type

The study on the mechanism of Maiwei Yangfei Decoction in anti-pulmonary fibrosis based on mitochondrial autophagy/glycolysisClinical observation of the efficacy of Maiwei Yangfei decoction in treating fibrotic interstitial lung disease of Qi-Yin deficiency type

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ITMCTR
Registry ID
ITMCTR2024000474
Enrollment
Unknown
Registered
2024-09-25
Start date
2024-12-01
Completion date
Unknown
Last updated
2024-10-14

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

Conditions

Pulmonary fibrosis

Interventions

Maiwei Yangfei Decoction Group:Add Maiwei Yangfei Decoction on top of standardized Western medical treatment.
Control Group:Receives standardized symptomatic treatment according to Western medicine which includes pharmacological treatment with pirfenidone nintedanib and N-acetylcysteine as well as non-pharmac

Sponsors

Jiangsu Province Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Meets the diagnostic criteria for fibrotic interstitial lung disease according to Western medicine. 2. Meets the diagnostic criteria for Qi and Yin deficiency syndrome according to Traditional Chinese Medicine. 3. Aged between 40 and 85 years regardless of gender. 4. Provides informed consent and volunteers to participate in the study.

Exclusion criteria

Exclusion criteria: 1. Patients in the acute phase or those with severe pulmonary infections or other critical conditions. 2. Patients with severe primary heart liver lung kidney blood disorders or other serious diseases affecting survival such as renal failure or heart failure. 3. Pregnant or breastfeeding women. 4. Individuals who cannot provide fully informed consent due to intellectual or behavioral impairments. 5. Suspected or confirmed history of alcohol or drug abuse. 6. Other conditions as judged by the researcher that may reduce the likelihood of enrollment or complicate enrollment such as frequently changing work environments that could lead to loss to follow-up. 7. Individuals with allergies such as a history of allergies to two or more drugs or foods; or known allergies to any component of the study drug. 8. Patients currently participating in other clinical drug trials.

Design outcomes

Primary

MeasureTime frame
Traditional Chinese Medicine Symptom Scoring;

Secondary

MeasureTime frame
6-Minute Walk Distance;SpO2%;Lung Function;Number of Acute Exacerbations;Visual Semi-Quantitative Assessment of Chest HRCT;Serum Lactate Levels;Serum IL-6 and TGF-ß Levels;St. George's Respiratory QuestionnaireSGRQ;

Countries

China

Contacts

Public ContactXianmei Zhou

Jiangsu Province Hospital of Chinese Medicine

zhouxianmeijs@aliyun.com13951035477

Outcome results

None listed

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