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The effects of sodium pentaborate (NaB) supplementation on calculi status and related metabolic risk factors in patient with kidney stone

The effects of sodium pentaborate (NaB) supplementation on calculi status and related metabolic risk factors in patient with kidney stone

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20090609002017N34
Enrollment
120
Registered
2019-04-07
Start date
2019-06-21
Completion date
Unknown
Last updated
2019-04-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

kidney stone. Calculus of kidney and ureter

Interventions

Intervention 1: intervention group: n= 80. Patients in this group will receive 2 capsules of sodium pentaborate (NaB) supplements for 8 weeks daily . each capsules contain 5 mg sodium pentaborate (Na

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: Men and women aged 20-50 years Patients with kidney stones with urologist diagnosis (other than obstructive, infectious, and ureter stones) Patients with kidney stones who, can be follow with drug therapy for a maximum of 3 month,according to a urologist diagnosis Not suffering from liver and kidney failure Patients who are willing to participate in the study

Exclusion criteria

Exclusion criteria: Pregnancy or lactation Suffering from other kidney related metabolic disorders and disease, at the same time Smoking Having a special diet Patients with obstructive stones, infections, and ureter stones and Emergency cases requiring special treatment or surgery with the diagnosis of urologists Changes in the drug protocol during the study

Design outcomes

Secondary

MeasureTime frame
Values of liver functional tests (ALT_AST_ALP). Timepoint: Before and after treatment. Method of measurement: Enzymatic methods.;Urine culture status. Timepoint: Before and after treatment. Method of measurement: Standard methods.;Dietary status (Dietary intake and Appetite). Timepoint: Before and after treatment. Method of measurement: FFQ and VAS questionnaires.;Serum levels of oxidative Stress indices (Malondialdehyde (MDA) and Total antioxidant capacity). Timepoint: Before and after treatment. Method of measurement: Spectrophotometry.;Status of some blood indices [PT(prothrombin time), ESR (erythrocyte sedimentation rate), INR (International Normalized Ratio), Albumin]. Timepoint: Before and after treatment. Method of measurement: Standard method, Westergren, Calculate, ELISA kit.

Primary

MeasureTime frame
Calculi status. Timepoint: Weeks 0, 4 and 8 study. Method of measurement: Ultra sonography.;Values of kidney functional tests (Urea, Creatinin, BUN, Uric acid, Analysis of urinary ions (Ca, k, Na), Serum PTH). Timepoint: Before and after treatment. Method of measurement: Enzymatic methods, Atomic absorption, ELISA kit.;Status of metabolic syndrome. Timepoint: Before and after treatment. Method of measurement: Measurement of blood pressure with stethoscope, Measurement of waist circumference , Measurement of HDL-cholesterol, triglyceride, FBS and fasting Insulin through enzymatic methods.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Behrooz

Tabriz University of Medical Sciences

mm.behroozp@gmail.com+98 41 3335 2292

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026