Modified Sini Powder (MSNP) improves depressive symptoms in postoperative NSCLC patients with mild-to-moderate depression
This protocol describes a multicenter, randomized, double-blind, placebo-controlled trial evaluating MSNP for postoperative depression in NSCLC patients. The primary outcome is a ≥25% reduction in the 17-item Hamilton Depression Rating Scale score after 6 weeks of treatment. The trial aims to provide robust clinical evidence and explore multi-omics mechanisms.
Evidence Score
Study Evidence
Study 1. Modified sini powder for the management of postoperative depression in non-small cell lung cancer patients: a multicenter, randomized, double-blind, placebo-controlled trial protocol.
observationalJin Y, Wang J, Li H, Fan M, Zhang S, Lin B, Mi Y, Gong C, Gu P, Xu K, Zhao B, Lang J, Chen M · Frontiers in pharmacology (2026)
Result:
Mechanism Graph
Limitations
- ⚠This is a protocol paper; no results are yet available to confirm efficacy or safety.
- ⚠The trial relies on subjective depression rating scales, which may introduce bias despite blinding.
- ⚠Generalizability may be limited to Chinese populations and specific healthcare settings.
Frequently Asked Questions
What is Modified Sini Powder (MSNP)?▼
MSNP is a modified traditional Chinese medicine formula derived from classical Sini Powder, used to alleviate depressive symptoms.
How long is the treatment period in this trial?▼
The intervention lasts for 6 weeks.
What is the primary outcome measure?▼
The primary outcome is the total effective rate, defined as a ≥25% reduction in the 17-item Hamilton Depression Rating Scale score from baseline at the end of treatment.
How many participants are being recruited?▼
468 postoperative NSCLC patients with mild-to-moderate depression will be recruited across nine tertiary medical centers.
Products
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References
- 1.Jin Y, Wang J, Li H, Fan M, Zhang S, Lin B, Mi Y, Gong C, Gu P, Xu K, Zhao B, Lang J, Chen M. "Modified sini powder for the management of postoperative depression in non-small cell lung cancer patients: a multicenter, randomized, double-blind, placebo-controlled trial protocol.." Frontiers in pharmacology, 2026. PMID: 42403716 DOI: 10.3389/fphar.2026.1805554