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Not Yet RecruitingNCT07185308

Postbiotics Ameliorate Cachexia in Patients With Non-small-cell Lung Cancer

Postbiotics Ameliorate Cancer Cachexia in Patients With Non-small-cell Lung Cancer: a Multicentre, Double-blind, Randomised Controlled Trial

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
150 (estimated)
Sponsor
Daping Hospital and the Research Institute of Surgery of the Third Military Medical University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study aims to evaluate the efficacy of the oral postbiotic preparation JK-5G in improving body weight among patients with non-small-cell lung cancer (NSCLC)-related cachexia. By means of a randomized controlled trial, we will compare the between-group difference in body-weight changes between the JK-5G and placebo arms to clarify its nutritional therapeutic benefit.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTPostbiotics, 2.5 g per dose, three times per dayPostbiotics oral powder, 2.5 g per dose, administered three times daily for a total duration of 90 days (four 21-day chemotherapy cycles).
DIETARY_SUPPLEMENTPlacebo, 2.5 g per dose, three times per dayPlacebo made of cyclodextrine, oral powder, 2.5 g per dose, administered three times daily for a total duration of 90 days (four 21-day chemotherapy cycles).

Timeline

Start date
2025-11-01
Primary completion
2026-12-31
Completion
2026-12-31
First posted
2025-09-22
Last updated
2025-09-25

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07185308. Inclusion in this directory is not an endorsement.