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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT01973088
Other study ID # Southwest Hospital,TMMU
Secondary ID
Status Active, not recruiting
Phase N/A
First received October 20, 2013
Last updated December 8, 2013
Start date November 2013

Study information

Verified date September 2013
Source Southwest Hospital, China
Contact n/a
Is FDA regulated No
Health authority China: Ethics Committee
Study type Observational

Clinical Trial Summary

This study intends to use in patients with renal tissue and blood samples, screening and identification of renal tissue hURAT1 regulating the expression of micro-RNA, for further study of uric acid stone formation mechanism and the occurrence of clinical preventive uric acid stones provide new clues and new intervention targets.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 80
Est. completion date
Est. primary completion date June 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

A?B group were enrolled standards: ? aged 18-65 years old; ? comply with percutaneous nephrolithotomy lithotripsy indications for surgery; ? ECT tips ipsilateral normal or mildly impaired renal function.

Group C patients were enrolled standards: ? aged 18-65 years old; ? normal renal function, not associated with urinary calculi in patients; ? cancer patients met radical nephrectomy indications for surgery; ? emergency trauma patients suffering from kidney resection surgical indications.

Exclusion Criteria:

- aged <18 years or> 65 years; ? neurological disease or cognitive dysfunction; ? can not be corrected or uncorrected coagulopathy; ? associated with diabetes, hypertension and other metabolic diseases; ? accompanied by tuberculosis, hepatitis, HIV and other infectious diseases; ? poor tolerance to anesthesia and surgery, such as: severe cardiopulmonary disease, coagulation disorders, etc.; ? ultrasound, renal imaging examination revealed renal cortex was significantly thinner (renal cortical thickness <1.5cm), structural variation; ? with severe systemic or urinary tract infection; ? ECT tips ipsilateral renal function is severely impaired or solitary kidney.

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Qian-wei Li

Outcome

Type Measure Description Time frame Safety issue
Primary micro-RNA microRNA microarray:the micro-RNA of kidney tissue 6 months No
Secondary Urine Urine Analyzer:Urine color, transparency, pH, erythrocytes, leukocytes, epithelial cells, casts, protein, specific gravity, and qualitative urine 24 hours No
Secondary 24h urine quantitative analysis Urine Analyzer:Urine, sodium, potassium, calcium, magnesium, ammonium, phosphate, sulfate, uric acid, oxalate, citrate, creatinine 96 hours No
Secondary Blood biochemistry Blood biochemical analyzer:Sodium, potassium, chloride, calcium, phosphorus, magnesium, bicarbonate, uric acid, creatinine 24 hours No
Secondary Stone analysis Infrared Spectroscopy:Calcium oxalate monohydrate , carbonated apatite, calcium oxalate dihydrate ,anhydrous uric acid, urine ammonium,magnesium ammonium phosphate 3 weeks No
Secondary hURAT1 transporter protein WESTERN BLOT?RT-qPCR:hURAT1 transporter protein of kidney tissue 6 months No
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