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Xiaozhenjiedu formula for EGFR-TKIs-related skin rash in lung cancer patients: a prospective, randomized controlled, phase II trial

Xiaozhenjiedu formula for EGFR-TKIs-related skin rash in lung cancer patients: a prospective, randomized controlled, phase II trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800020249
Enrollment
Unknown
Registered
2018-12-21
Start date
2019-01-01
Completion date
Unknown
Last updated
2019-01-14

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

Conditions

EGFR-TKIs-related skin rash

Interventions

integrative medicine group:Xiaozhenjiedu formula+Erythromycin Ointment
CHM group:Xiaozhenjiedu formula

Sponsors

Oncology Department, Guangdong Provincial Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Diagnosed with non-same cell lung cancer by pathology and has been receiving EGFR-TKIs treatment; 2. Had the skin rash related EGFR-TKIs; 3. Aged 18 years or older; 4. Estimated survival time more than 3 months; 5. Normal function of bone marrow, liver, kidney, heart and lung; 6. Can understand the study well and sign the written informed consent.

Exclusion criteria

Exclusion criteria: 1. The skin of the affected area is damaged; 2. Combine with other tumors; 3. Combine with active tuberculosis and other serious infectious diseases; 4. Have received chemotherapy, radiotherapy, other targeted therapy or immunopreparations within the last two months; 5. Received orally Chinese herbal medicine or Chinese patent medicine with a function of clearing heat and resolving toxins, such as jinyinhua ???, kushen ??, in the course of trial; 6. Have serious brain or mental illness, or have no legal capacity to prosecute, medical or ethical reasons affect the continuation of the study; 7. Have the history of organ transplantation (including autologous bone marrow transplantation and peripheral stem cell transplantation); 8. Pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
Papulopustular rash;

Secondary

MeasureTime frame
FACT-L, KPS;Adverse events;Response Rate;

Countries

China

Contacts

Public ContactYihong Liu

Guangdong Provincial Hospital of Chinese Medicine

viktim@163.com+86 18928840816

Outcome results

None listed

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