Mature Vinegar Prophylaxis Against Recurrent Calcium Oxalate Nephrolithiasis
Primary Purpose
Nephrolithiasis
Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
mature vinegar
placebo (water)
Sponsored by
About this trial
This is an interventional prevention trial for Nephrolithiasis focused on measuring calcium oxalate, nephrolithiasis, Mature vinegar, prophylaxis
Eligibility Criteria
Inclusion Criteria:
- Male and female > 18 years;
- History of recurrent nephrolithiasis, with one or more calcium oxalate or mixed (calcium oxalate and phosphate, calcium oxalate and uric acid) stone formation over the last 5 years; the stone had been removed completely confirmed by CT scan;
- No current treatment for the prevention of recurrent stones except for the advice to increase water intake;
- Residence in the area of Guangzhou, China;
- Written informed consent
Exclusion Criteria:
- Obstructive uropathy, chronic urosepsis, renal failure (serum creatinine > 177 umol/L), renal tubular acidosis, primary hyperparathyroidism, primary hyperoxaluria, bowel resection, inflammatory bowel disease, pure uric acid and cystine stones, medullary sponge kidney;
- Active peptic ulcer disease, gastric esophagus reflux; Past history of peptic ulcer disease;
- Participants who had a known the vinegar effect for stone formation;
- Concomitant clinical conditions that might affect completion of the study or jeopardize data interpretation.
Sites / Locations
- The First Affiliated Hospital of Guangzhou Medical UniversityRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Experimental
Arm Label
Control group
Intervention group
Arm Description
Administer 5 ml placebo (purified water) three times a day.
Administer 5 ml mature vinegar (Brand: Ninghuafu) three times a day.
Outcomes
Primary Outcome Measures
Recurrence rate of renal stone
The first recurrence of a symptomatic renal stone or the presence of asymptomatic renal stone or the presence of a radiographically identified stone.
Secondary Outcome Measures
24-h urine compositions
Change in 24-h urine compositions (calcium excretion, oxalate excretion, etc.)
serum calcium
Change in serum calcium
serum creatinine
Change in serum creatinine
serum uric acid
Change in serum uric acid
Full Information
NCT ID
NCT03092908
First Posted
March 22, 2017
Last Updated
June 29, 2018
Sponsor
The First Affiliated Hospital of Guangzhou Medical University
1. Study Identification
Unique Protocol Identification Number
NCT03092908
Brief Title
Mature Vinegar Prophylaxis Against Recurrent Calcium Oxalate Nephrolithiasis
Official Title
Mature Vinegar Prophylaxis Against Recurrent Calcium Oxalate Nephrolithiasis - a Prospective Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
June 2018
Overall Recruitment Status
Unknown status
Study Start Date
March 22, 2017 (Actual)
Primary Completion Date
December 31, 2021 (Anticipated)
Study Completion Date
December 31, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
The First Affiliated Hospital of Guangzhou Medical University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Kidney stones are one of the most common disorders of the urinary tract and cause a great deal of morbidity and economic loss. Because of the high recurrence rate, researchers are interested in finding medicinal therapies to prevent kidney stone recurrence. Vinegar is consumed worldwide as a food condiment and preservative. The mature vinegar, also called black vinegar, is an inky-black vinegar aged for a malty, woody, and smoky flavor. It is popular in the north of China as a dipping sauce, particularly for dumplings.
Some studies promote vinegar for its medicinal properties, as a tonic which may lower blood pressure and cholesterol level. Our national epidemiological data in China showed that consumed more mature vinegar was associated with decreased risk of kidney stones formations. Furthermore, our previous in vivo study found that mature vinegar could inhibit renal calcium oxalate crystals formation in rat model. These findings inspire us to clarify the nephrolithiasis prevention effect of mature vinegar in a clinical trial. In this study, investigators would like to examine the efficacy of mature vinegar prophylaxis for preventing recurrent calcium oxalate nephrolithiasis.
Detailed Description
Background: Kidney stones are one of the most common disorders of the urinary tract and cause a great deal of morbidity and economic loss. Because of the high recurrence rate, researchers are interested in finding medicinal therapies to prevent kidney stone recurrence. Vinegar is consumed worldwide as a food condiment and preservative. The mature vinegar, also called black vinegar, is an inky-black vinegar aged for a malty, woody, and smoky flavor. It is popular in the north of China as a dipping sauce, particularly for dumplings.
Some studies promote vinegar for its medicinal properties, as a tonic which may lower blood pressure and cholesterol level. Our national epidemiological data in China showed that consumed more mature vinegar was associated with decreased risk of kidney stones formations. Furthermore, our previous in vivo study found that mature vinegar could inhibit renal calcium oxalate crystals formation in rat model (unpublished). These findings inspire us to clarify the nephrolithiasis prevention effect of mature vinegar in a clinical trial. In this study, investigators would like to examine the efficacy of mature vinegar prophylaxis for preventing recurrent calcium oxalate nephrolithiasis.
Methods: A prospective randomized, controlled, single-center clinical trial will be performed at the First Affiliated Hospital of Guangzhou Medical University from March 2017 to March 2022.
Intervention: 80 subjects are randomly assigned in a 1:1 ratio to receive mature vinegar or placebo. The sequence of randomization is computer generated and are performed by the hospital's pharmacy service, whoever administer 5 ml mature vinegar (Brand: Ninghuafu) three times a day and placebo as liquid of the same type in identical bottles. The subjects, the attending urologist, and the investigators are not aware of study arm assignments until the final assessment of outcome.
From the beginning of invention, participants will be scheduled to receive a brief (< 10 min) individual telephone contact once per month and weekly text messages. The telephone contacts are conducted by intervention staff and followed a standard script. Text message are provided once per week and are used to remind participants in invention group of drinking mature vinegar.
Sample size estimation: According to non-continuous sample size calculation formula, , where P1 is 3-year stone recurrence rate in normal group , P2 is 3-year recurrence rate in mature vinegar group, P is (P1 + P2)/2. According to our preliminary clinical data, the 3-year stone recurrence rate in normal group between 30% and 50%. Assume P1 =40%. The vinegar invention would reduce the risk of recurrence by about three fourth. The 3-year stone recurrence rate after mature vinegar is 10% (P2). Using 95% confidence interval, an α error of 5%, and a power of 80%, the minimum sample size was estimated to be 32 subjects for each of the study groups. To account for subjects lost to follow-up and study withdrawals, this number is increased to 40.
Data collection and follow-up: Each subject's medical history is taken, a physical examination is performed, and the subject's weight, height, body mass index, blood pressure, education, income, employment status, smoking status, and alcohol consumption are measured and recorded. Assessment staff are masked to prior data at each assessment to minimize potential bias.
24-h urine and serum specimens are obtained at baseline (with values documented as the average of the two sets of measurements performed before randomization), 3 months after rafter randomization, half a year after randomization, and at yearly intervals during the 3 years of the study.
Outcome Measures: The primary outcome measure is the time to the first recurrence of a symptomatic renal stone or the presence of asymptomatic renal stone or the presence of a radiographically identified stone. In the event of a recurrence, the treatment is considered to have failed, and the patient will be withdrawn from the trial. If there are no recurrences, patients will be followed until the third annual visit (month 36). Patients who required treatment with thiazides or allopurinol for conditions such as hypertension or gout will be withdrawn from the trial.
Recurrences are considered to be either silent or symptomatic. Silent recurrences are diagnosed on the basis of renal ultrasound performed at 3 months, 6 months, 1 year, 2 year, 3 year after randomization. If renal stones are detected, CT will also be performed. The imaging studies will be performed by a central radiologic service, and the radiologist have no knowledge of the trial or the group assignment. A recurrence is classified as silent if a previously unreported stone was detected in the absence of symptom. A symptomatic recurrence is defined as typical renal colic, an episode hematuria, or the expulsion or removal of a previously undiscovered stone. If a symptomatic recurrence is documented on the basis of renal colic or hematuria, the recurrence will to be confirmed radiographically.
Secondary outcome measures include change in 24-h urine compositions (calcium excretion, oxalate excretion, etc.), serum calcium, phosphate, creatinine, and uric acid.
Statistical Analysis: The analysis is based on the intention-to-treat principle. Investigators use Kaplan-Meier analyses to determine the cumulative incidence of recurrent stones, and investigators use Cox proportional-hazards regression to determine the crude and adjust relative risks of recurrence.
For the analysis of the urinary indexes, investigators compare the two groups with respect to the absolute change from the base-line value at each time point. These comparisons are carried out with use of the Mann-Whitney test. Base-line continuous variables are compared with use of the Mann-Whitney test and Student's t-test whenever appropriate; categorical variables are compared with use of Fisher's exact test. A P value of less than 0.05 is considered to indicate statistical significance. All reported P values are two-side.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nephrolithiasis
Keywords
calcium oxalate, nephrolithiasis, Mature vinegar, prophylaxis
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
80 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Control group
Arm Type
Placebo Comparator
Arm Description
Administer 5 ml placebo (purified water) three times a day.
Arm Title
Intervention group
Arm Type
Experimental
Arm Description
Administer 5 ml mature vinegar (Brand: Ninghuafu) three times a day.
Intervention Type
Dietary Supplement
Intervention Name(s)
mature vinegar
Intervention Description
Administer 5 ml mature vinegar (Brand: Ninghuafu) three times a day.
Intervention Type
Dietary Supplement
Intervention Name(s)
placebo (water)
Intervention Description
Administer 5 ml placebo (water) three times a day.
Primary Outcome Measure Information:
Title
Recurrence rate of renal stone
Description
The first recurrence of a symptomatic renal stone or the presence of asymptomatic renal stone or the presence of a radiographically identified stone.
Time Frame
3 years
Secondary Outcome Measure Information:
Title
24-h urine compositions
Description
Change in 24-h urine compositions (calcium excretion, oxalate excretion, etc.)
Time Frame
3 years
Title
serum calcium
Description
Change in serum calcium
Time Frame
3 years
Title
serum creatinine
Description
Change in serum creatinine
Time Frame
3 years
Title
serum uric acid
Description
Change in serum uric acid
Time Frame
3 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Male and female > 18 years;
History of recurrent nephrolithiasis, with one or more calcium oxalate or mixed (calcium oxalate and phosphate, calcium oxalate and uric acid) stone formation over the last 5 years; the stone had been removed completely confirmed by CT scan;
No current treatment for the prevention of recurrent stones except for the advice to increase water intake;
Residence in the area of Guangzhou, China;
Written informed consent
Exclusion Criteria:
Obstructive uropathy, chronic urosepsis, renal failure (serum creatinine > 177 umol/L), renal tubular acidosis, primary hyperparathyroidism, primary hyperoxaluria, bowel resection, inflammatory bowel disease, pure uric acid and cystine stones, medullary sponge kidney;
Active peptic ulcer disease, gastric esophagus reflux; Past history of peptic ulcer disease;
Participants who had a known the vinegar effect for stone formation;
Concomitant clinical conditions that might affect completion of the study or jeopardize data interpretation.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Guohua Zeng, Ph.D. & M.D.
Phone
+8613802916676
Email
gzgyzgh@vip.sina.com
Facility Information:
Facility Name
The First Affiliated Hospital of Guangzhou Medical University
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510120
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Guohua Zeng, Ph.D.
Phone
+86 13802916676
Email
gzgyzgh@vip.sina.com
First Name & Middle Initial & Last Name & Degree
Guohua Zeng, M.D.
First Name & Middle Initial & Last Name & Degree
Wei Zhu, Ph.D.
12. IPD Sharing Statement
Learn more about this trial
Mature Vinegar Prophylaxis Against Recurrent Calcium Oxalate Nephrolithiasis
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