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Efficacy Study of Clinical Nutrition to Treat Lung Neoplasms And Breast Carcinoma

C

Chinese PLA General Hospital (301 Hospital)

Status

Completed

Conditions

Lung Neoplasms
Breast Neoplasms

Treatments

Drug: Maitake mushroom extract compound
Drug: Ginseng compound
Drug: GLSE compound

Study type

Interventional

Funder types

Other

Identifiers

NCT02603016
PLAGHS201503601

Details and patient eligibility

About

This study evaluates the efficacy of clinical nutrition to treat lung neoplasms and breast carcinoma.We estimate there will be 480 patients accepted.120 patients will receive GLSE compound,120 patients will recrive Maitake mushroom extract compound,120 patients will recrive Rinseng compound,and 120 patients will be as blank countrol group.Efficacy Study of Clinical Nutrition to Treat Lung Neoplasms And Breast Carcinoma

Full description

GLSE compound、Maitake mushroom extract compound and Rinseng compound have different mechanism on enhancing immunity.This clinicaltrial compare them the immune effect in the progress of treating lung neoplasms and breast carcinoma.Within the 42 days,we will abide by the plan to evaluate the immunity enhancement by monitoring mmune effector molecules.

Enrollment

480 patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • lung cancer and breast cancer patients confirmed by surgery pathology;
  • ECOG physical stamina score of 0~3 points;
  • Expected lifetime > 3 months;
  • Need to receive radiation and chemotherapy;
  • Heart, liver and kidney function and blood picture is normal,WBC≥4×109/L, neutrophil count≥ 2 x 109 / L,platelet count≥100×109/L, hemoglobin≥100 g/L;
  • To follow-up, good adherence

Exclusion criteria

  • Allergic to text drug;
  • Pregnancy or lactation women;
  • Suffering from mental illness of not easy to control,
  • Have serious mental or cognitive dysfunction;
  • Can not comply with the experimental scheme or can't cooperate with the follow-up;
  • The patients who are unfavorable to the subject.

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

480 participants in 4 patient groups

GLSE compound group
Experimental group
Description:
GLSE compound 2g each time by mouth,twice a day for 42 days.
Treatment:
Drug: GLSE compound
Maitake mushroom extract compound group
Experimental group
Description:
Maitake mushroom extract compound 2 tables each time by mouth,twice a day for 42 days.
Treatment:
Drug: Maitake mushroom extract compound
Ginseng compound group
Experimental group
Description:
Ginseng compound 2 tables each time by mouth,twice a day for 42 days.
Treatment:
Drug: Ginseng compound
blank control group
No Intervention group
Description:
Take nothing.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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