Chronic pruritus
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: a. All cases were clinically or pathologically diagnosed as non-small cell lung cancer, the clinicopathological staging criteria were patients with stage II or lower, and genetic testing met the EGFR-TKI medication criteria; b. patients diagnosed with chronic pruritus; c.KPS (Karnofsk) score > 60 points, and the expected survival was more than 6 months; d. aged 18-70 years, primary school or above culture; e. stable condition, no severe heart, liver, brain, kidney and other organ damage or bone marrow hematopoietic dysfunction and bleeding risk; f. patients with clear consciousness, no dyslexia, can complete the questionnaire; g. patients agreed to participate in this clinical study, and signed the informed consent form.
Exclusion criteria
Exclusion criteria: a. clinical and imaging judgment of disease progression, patients who need to adjust the medication regimen; b. patients who need chemotherapy, targeted, immunotherapy during the study; c. patients who use other antipruritic drugs during the study;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Modified DUO Pruritus Score; | — |
Secondary
| Measure | Time frame |
|---|---|
| VAS score;DLQI score;Expression levels of serum TRPV1, PKC, SP, and PGE-2; | — |
Countries
China
Contacts
The First Affiliated Hospital of Anhui University of Chinese Medicine