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High attrition rate up to 37.7% at one year's follow-up
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| Name | Class |
|---|---|
| The First Affiliated Hospital of Nanchang University | OTHER |
| Second Affiliated Hospital of Nanchang University | OTHER |
| Jiangxi Provincial Cancer Hospital | OTHER |
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This trial aims to determine whether Hou Gu Mi Xi is an effective treatment for improving symptoms and indicators in patients with spleen qi deficiency and radical gastrectomy for gastric cancer.
The incidence of gastric cancer ranks high in many countries around the world. Although along with the development of economy and medical condition the incidence of gastric cancer appears a trend of decrease in developed countries, it is still one of most common cancers in Asia. There are more new gastric cancer cases in China compared with other countries every year. According to an epidemiological survey by World Health Organization, 5-year prevalence of gastric cancer was 53.7/10,000 in China - it is only lower than Japan. For the early gastric cancer, radical gastrectomy, is the most important treatment, which could significantly prolong disease-free survival and overall survival. However, the severe damage of surgery and following radiation and chemotherapy in intestinal tract usually leads patients to be a constitution of spleen qi deficiency, a concept of traditional Chinese medicine (TCM) that mainly involves digestive symptoms, such as poor appetite, abnormal stool (loose, diarrhea) and abdominal distention. Therefore, how to resolve and protect the function of intestinal tract, and change the constitution of spleen qi deficiency postoperatively is important for improving quality of life and reducing the recurrence rate of cancer.
Shen Ling Bai Zhu San, a classic Chinese medicinal formulae originally described in Tai Ping Hui Min He Ji Ju Fang in the Song Dynasty (1102 AD), is composed of ginseng, tuckahoe, atractylodes, baked licorice, coixenolide, Chinese yam, lotus seed, shrinkage fructus amomi, platycodon grandiflorum, white hyacinth bean, and dried orange peel. It has effects of replenishing qi and invigorating spleen (spleen is a TCM conception that differs from western medicine), as well as penetrating wet and antidiarrheal. It is mainly used for treating the syndrome of spleen qi deficiency, including dyspepsia, chest and stomach distress, borborygmus and diarrhea, limb weakness, thin body, sallow complexion, pale tongue with white and greasy coating, and weak and slow pulse, etc. In the theory of TCM, spleen is the source for producing qi and blood and thus is the root of life. Shen Ling Bai Zhu San could invigorate spleen by supplying spleen and remove wet, and finally nourish the stomach and intestine. Previous pharmacologic studies also revealed that Shen Ling Bai Zhu San could adjust function of anaerobic and aerobic bacteria in gastrointestinal tract; specifically, it could improve the proliferation of probiotics (such as bifidobacterium) and inhibit the main resistance strains (such as enterococcus) and thus has an effect to improve gastrointestinal symptoms.
According to the experience of TCM, the constitution of patients who are undergoing radiation and chemotherapy is usually yin deficiency, but changes to spleen qi deficiency due to digestive disorders after those treatment. Therefore, Shen Ling Bai Zhu San is expected to improve symptoms in patients who underwent gastrectomy and following radiation and chemotherapy.
Hou Gu Mi Xi is a dietary therapy form of Shen Ling Bai Zhu San, which removes atractylodes and platycodon grandiflorum (two herbs that could not be used as food) from Shen Ling Bai Zhu San, and adds perilla leaf for adapting a dietary therapy for a long-term use. Hou Gu Mi Xi uses the main formula of Shen Ling Bai Zhu San, so that it could theoretically maintain the treatment effects. Although the reliable health effects of Shen Ling Bai Zhu San has been proved in previous studies, Hou Gu Mi Xi is optimized in formula and its preparations changed from electuary to rice paste, so that its functional mechanism and efficacy may be different. Therefore, the investigators plan to perform a hospital-based randomized controlled trial, enroll patients from three hospitals in Nanchang City of Jiangxi Province in China, for assessing efficacy and safety of Hou Gu Mi Xi on digestive symptoms in patients with spleen qi deficiency and radical gastrectomy for gastric cancer.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Hou Gu Mi Xi | Experimental | Patients in this arm receive Hou Gu Mi Xi, with an oral dose of 10 g/day during entire follow up period (2 years). |
|
| placebo | Placebo Comparator | Patients in this arm receive placebo, with an oral dose of 10 g/day during entire follow up period (2 years). |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Hou Gu Mi Xi | Dietary Supplement | Hou Gu Mi Xi is a dietary therapy form of Shen Ling Bai Zhu San, which removes atractylodes and platycodon grandiflorum, adds perilla leaf for adapting a dietary therapy. |
| Measure | Description | Time Frame |
|---|---|---|
| Changes from baseline in total scores of Spleen Qi Deficiency Symptoms Grading and Quantifying Scale (Units on a scale) | Higher score indicates severer symptoms of Spleen Qi Deficiency. Units of measure (Units on a scale) | At baseline and 2, 4, 8, 26, 52, 78 and 104 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Qualitative assessment of changes in total scores of SQD scale from baseline | 1) completely remission: reduction in scores is ≥ 95% compared with baseline; 2) markedly effective: reduction in scores is 70% to 94% compared with baseline; 3) effective: reduction in scores is 30% to 69% compared with baseline; 4) not effective: reduction in scores is < 30% compared with baseline | At baseline and 2, 4, 8, 26, 52, 78 and 104 weeks |
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Inclusion Criteria:
Patient should be diagnosed as gastric cancer by pathology and have received radical gastrectomy. They should finish the following radiotherapy and chemotherapy and the treatment for surgical complications (such as leak, stricture, and marginal ulcer).
Patient should be constitution of spleen qi deficiency, that is, meet two primary symptoms of spleen deficiency + two primary symptoms of qi deficiency, or meet two primary symptoms of spleen deficiency + one primary symptoms of qi deficiency + one auxiliary symptoms, or meet one primary symptoms of spleen deficiency + one primary symptoms of qi deficiency + two secondary symptoms + one auxiliary symptoms as follow:
Age ranges from 18 to 70 years; both male and female
Patient should be in fair performance status, indicated by a score of Eastern Cooperative Oncology Group (ECOG) Performance Status ≤ 1
Sign the informed consent
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Weifeng Zhu, Ph.D. | Jiangxi University of Traditional Chinese Medicine | Study Chair |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Jiangxi University of Traditional Chinese Medicine | Nanchang | Jiangxi | 330004 | China |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 27433390 | Background | Oh SY, Lee HJ, Yang HK. Pylorus-Preserving Gastrectomy for Gastric Cancer. J Gastric Cancer. 2016 Jun;16(2):63-71. doi: 10.5230/jgc.2016.16.2.63. Epub 2016 Jun 24. | |
| 16440411 | Background | Yang L. Incidence and mortality of gastric cancer in China. World J Gastroenterol. 2006 Jan 7;12(1):17-20. doi: 10.3748/wjg.v12.i1.17. |
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The investigators do not plan to share individual participant data.
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| ID | Term |
|---|---|
| D013274 | Stomach Neoplasms |
| D005767 | Gastrointestinal Diseases |
| ID | Term |
|---|---|
| D005770 | Gastrointestinal Neoplasms |
| D004067 | Digestive System Neoplasms |
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
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| placebo | Other | The placebo has same appearance, taste and smell as Hou Gu Mi Xi. |
|
| Changes in scores of each item of SQD scale from baseline | 1) Stomach distension*, 2) Abdominal distension*, 3) Fatigue and weakness*, 4) Tired mind and taciturnity*, 5) Inappetence*, 6) Stomach pain, 7) Stomach tightness, 8) Abdominal pain, 9) Acid reflux, 10) Belching, 11) Nausea and vomiting, 12) Abnormal stools, 13) Abnormal bowel sounds, 14) Powerless defecation, 15) Sallow complexion, 16) Tastelessness and hypodipsia, and 17) Face and limbs edema. | At baseline and 2, 4, 8, 26, 52, 78 and 104 weeks |
| Changes from baseline in total scores of Short Form 36 (SF-36) (Units on a scale) | To assess quality of life | At baseline and 2, 4, 8, 26, 52, 78 and 104 weeks |
| Changes from baseline in scores of subitems in Short Form 36 (SF-36) (Units on a scale) | Physical Component Summary (PCS) and Mental Component Summary (MCS) | At baseline and 2, 4, 8, 26, 52, 78 and 104 weeks |
| Changes from baseline in scores of Eastern Cooperative Oncology Group (ECOG) Performance Status (Units on a scale) | To assess performance status | At baseline and 2, 4, 8, 26, 52, 78 and 104 weeks |
| Progression free survival (month) | assessed by evidence of pathological examination, computed tomography and/or magnetic resonance imaging | From the first dose of intervention up to 104 weeks |
| Changes from baseline in systolic blood pressure (mmHg) | To determine whether the interventions improve systolic blood pressure | At baseline and 2, 4, 8, 26, 52, 78 and 104 weeks |
| Changes from baseline in diastolic blood pressure (mmHg) | To determine whether the interventions improve diastolic blood pressure | At baseline and 2, 4, 8, 26, 52, 78 and 104 weeks |
| Changes from baseline in body weight (kg) | To determine whether the interventions improve body weight | At baseline and 2, 4, 8, 26, 52, 78 and 104 weeks |
| Changes from baseline in body mass index (kg/m2) | To determine whether the interventions improve body mass index | At baseline and 2, 4, 8, 26, 52, 78 and 104 weeks |
| Incidence of any adverse events | abnormal results (indicated by more or less than 2 × normal reference interval) in the routine blood, urine, and stool tests, liver function tests (alanine transaminase [ALT], aspartate aminotransferase [AST], total bilirubin [TBIL], direct bilirubin [DBIL], indirect bilirubin [IBIL]), kidney function tests (serum creatinine [SCr] and urea nitrogen [BUN]), coagulation function (prothrombin time [PT], activated partial thromboplastin time [APTT], thrombin time [TT], fibrinogen [FIB]), and electrocardiogram as well as any other new-onset symptoms or diseases related or unrelated to the intervention | From the first dose of intervention up to 104 weeks |
| Incidence of severe adverse events | AEs that lead to new or prolonged hospitalization, disability, admission to intensive care unit, life danger, and death | From the first dose of intervention up to 104 weeks |
| Incidence of drug-related adverse events | This outcome is assessed by blinded clinicians in each research center | From the first dose of intervention up to 104 weeks |
| Incidence of withdrawn due to adverse events | From the first dose of intervention up to 104 weeks |
| 20845514 | Background | Wu TH, Chen IC, Chen LC. Antacid effects of Chinese herbal prescriptions assessed by a modified artificial stomach model. World J Gastroenterol. 2010 Sep 21;16(35):4455-9. doi: 10.3748/wjg.v16.i35.4455. |
| 15788127 | Background | Yin GY, Chen Y, Shen XJ, He XF, Zhang WN. Study on the pathophysiologic basis of classification of 'spleen' deficiency in chronic gastritis. Chin Med J (Engl). 2005 Mar 20;118(6):468-73. |
| 15361303 | Background | Yin GY, Zhang WN, Shen XJ, He XF, Chen Y. Study on the pathological basis of classification of spleen deficiency in chronic gastritis. Chin Med J (Engl). 2004 Aug;117(8):1246-52. |
| 31182140 | Derived | Zhou X, Yan DM, Zhu WF, Liu WJ, Nie HY, Xu S, Jiang YP, Zhang KH, Fu Y, Wan YY, Yu XY, Li H, Sun X, Chen XF. Efficacy and safety of Hou Gu Mi Xi in patients with spleen qi deficiency syndrome who underwent radical gastrectomy for gastric cancer: protocol for a multicenter, randomized, double-blind, placebo-controlled trial. Trials. 2019 Jun 10;20(1):343. doi: 10.1186/s13063-019-3429-x. |
| D004066 |
| Digestive System Diseases |
| D013272 | Stomach Diseases |