Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT07524777

Ganoderma Spores Modulate the Gut-Brain Axis

Targeting the Gut-Brain Axis With Ganoderma Lucidum Spores Ameliorates Depression in Thyroid Cancer Patients: a Randomized, Double-blind, Placebo-controlled Trial

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
300 (estimated)
Sponsor
Ling Zhiqiang · Academic / Other
Sex
Female
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

This study aims to investigate whether Sporoderm-removed Ganoderma lucidum spore powder (RGLS) ameliorates depression in thyroid cancer patients through gut-brain axis modulation, and to elucidate the underlying microbial and metabolic mechanisms. This 3-month randomized, double-blind, placebo-controlled trial will enroll 300 postoperative papillary thyroid carcinoma patients with depressive symptoms (HAMD-24 ≥ 8). Participants will be randomly assigned(2 : 1) to receive RGLS (2 g/day) or matched placebo.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTSporoderm-removed Ganoderma lucidum spore powder (RGLS)From the first day after enrollment, subjects take RGLS orally at 4g/day for 3 months.
OTHERPlaceboFrom the first day after enrollment, subjects take placebo orally at 4g/day for 3 months.

Timeline

Start date
2026-04-15
Primary completion
2026-07-31
Completion
2026-08-31
First posted
2026-04-13
Last updated
2026-04-13

Source: ClinicalTrials.gov record NCT07524777. Inclusion in this directory is not an endorsement.