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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05631782
Other study ID # Caowenfu590
Secondary ID
Status Completed
Phase Early Phase 1
First received
Last updated
Start date November 10, 2020
Est. completion date December 26, 2021

Study information

Verified date November 2022
Source The First People's Hospital of Zunyi
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To explore the clinical effect of Shenkang Decoction in chronic renal failure (CRF) patients with hemodialysis (HD).


Recruitment information / eligibility

Status Completed
Enrollment 160
Est. completion date December 26, 2021
Est. primary completion date December 25, 2021
Accepts healthy volunteers No
Gender All
Age group 52 Years to 65 Years
Eligibility Inclusion Criteria: - The diagnosis of western medicine meets the diagnostic criteria of chronic kidney failure in Internal Medicine - the diagnosis of TCM meets the diagnostic criteria of the disease in the Guiding Principles for Clinical Research of New Chinese Medicine. - The patient is over 18 years old, - can think independently and have civil conduct, - strictly follow the doctor's advice, - maintain stable condition and regular HD treatment. Exclusion Criteria: - Patients with HD time of no more than three months, severe uncontrolled infection, other malignant diseases, heart, liver, brain, and digestive system dysfunction, mental diseases such as dementia or depression; - contraindications to HD or contraindications to the study (Shock or systolic blood pressure below 80mm/Hg, severe bleeding or a tendency to bleed, serious infection such as sepsis, or a blood-borne infection, advanced tumor, extremely debilitating or not cooperating with doctor) - drug allergy, chronic use of glucocorticoids, and immunosuppressants. - women during pregnancy or lactation.

Study Design


Intervention

Drug:
Shenkang decoction
Given Shenkang decoction on the basis of the above treatment. Shenkang decoction prescription: 15 g of semen cuscutae, herba epimedii and pericarpium arecae. 20 g of Eucommia ulmoides Oliv., radix astragali, codonopsis pilosula, salvia miltiorrhiza, tuckahoe, atractylodes macrocephala, Chinese yam, honeysuckle, polyporus umbellatus and dandelion. 15 g of safflower. 12 g of processed Fuzi. 10 g of Radix phytolaccae and sage. Golden cherry son 20 g and puzzle kernel 15 g were added to patients with frequent proteinuria and nocturia took. Yellow cypress 15 g was added to patients with damp-heat in lower-Jiao. The decoction pieces were purchased from the Traditional Chinese Medicine and Pharmacy Department of the First People's Hospital of Zunyi City. They were decocted by computer automatic decocting machine (model) and divided into 150 mL / bag, taken orally, once in the morning, noon and evening, 3 times / day, 1 bag / time, one pair a day. Treatment lasted for 10 - 14 days.

Locations

Country Name City State
China The First People's Hospital of Zunyi Zunyi

Sponsors (1)

Lead Sponsor Collaborator
The First People's Hospital of Zunyi

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Renal function index The AU5800 fully automatic biochemical analyzer produced by Beckman Coulter Co., Ltd. was selected for renal function index determination. peripheral venous blood (3-5 mL) was extracted before and after treatment, and Cre and urea nitrogen were measured after centrifugation 8 min
Primary TCM syndrome points According to the relevant contents of the Clinical Guiding Principles of New Chinese Medicine13, clinical symptoms of shortness of breath, fatigue, anorexia, chills, abdominal fullness and distension, unsolid stool, and weak waist were evaluated. 14 days
Primary Nutritional status index In patients, 3 mL of fasting venous blood was collected and given anticoagulant treatment. The total serum protein, serum albumin, hemoglobin, and total red blood cells were measured by Mindray automatic biochemical analyzer (model BS-280, Shenzhen Mindray Bio-Medical Electronics Co., LTD.). 14days
Primary Dialysis adequacy judgment index The urea dynamic model was used to evaluate the overall urea clearance judgment of a single dialysis effect, and Kt / V was calculated according to the Daugirdas formula. Kt / V= -ln (BUN before dialysis / BUN after dialysis-0.008 t) + (4-3.5 BUN before dialysis /BUN after dialysis) ultrafiltration volume / dialysis body weight. Long-term dialysis components are protein catabolism rate (calculated by Gotch formula) and time-average urea concentration (calculated by Lowrie formula). Protein catabolism rate = 9.35G×0.29Vt. 14 days
Primary Treatment efficiency The efficacy of the two groups was compared with the TCM syndrome points and the biochemical examination indexes. 14 days
Primary General physical examination Including heart rate, blood pressure, breathing, pulse, and urine volume. Urine routine, blood routine, stool routine, liver and kidney function testing, and electrocardiogram monitoring. 14 days
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