Fact CheckerSign in

NCT06429514Completed

Study on the Mechanism of Ganoderma Lucidum Spore Powder in the Treatment of Depression

Based on the Theory of Gut-brain Axis, the Intervention Effect and Related Mechanism of Ganoderma Lucidum Spore Powder on Depressive Symptoms in Patients With Thyroid Cancer Were Investigated

Source: ClinicalTrials.gov · Last updated 28 May 2024

Brief summary (registry, in English)

To clarify the clinical effect of Ganoderma lucidum spore powder intervention on postoperative depressive symptoms of papillary thyroid carcinoma ; to elucidate the antidepressant mechanism of Ganoderma lucidum spore powder.

Status (registry)
Completed
Study type
Interventional
Enrollment
298 (actual)
First submitted
15 May 2024
Start date
28 Mar 2023
Primary completion date
3 May 2024
Lead sponsor
Ling Zhiqiang
NCT number
NCT06429514

What you commit to

  • Study type: Interventional
  • Participants enrolled: 298
  • From 28 Mar 2023 to the primary completion date, 3 May 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Gastrointestinal surgery was performed before intervention
  • Including patients with other malignant tumors, who need chemotherapy, radiotherapy, biological therapy or traditional Chinese medicine treatment received antibiotics or microecological modulators within 3 months before the intervention

Other illness

  • suffering from other diseases of the intestinal system
  • Patients with severe depressive symptoms who must receive antidepressant treatment organic diseases such as heart and brain diseases, brain trauma history of mental illness, use of psychoactive drugs such as drugs

Other

  • Acute intestinal obstruction
  • Severe liver and kidney dysfunction
  • Pregnancy, lactation

Who the study is looking for

  • patients with depressive symptoms after surgery for papillary thyroid carcinoma in the outpatient department of Zhejiang Cancer Hospital
  • Han nationality
  • No previous depression and other mental diseases
  • 18-80 years old
  • Women
  • BMI 19 \~ 24

Age in the registry: 18 years to 80 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Zhejiang Cancer Hospital
Coordinator of this site? Confirm its status
HangzhouChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.