Overview

A Study on the Effection of Potassium Citrate Extended-release Tablets on Urolithiasis Formation or Recurrence

Status:
Unknown status
Trial end date:
2020-09-01
Target enrollment:
0
Participant gender:
All
Summary
Assess the efficacy and safety of potassium citrate extended-release tablets on Urolithiasis formation or recurrence.
Phase:
Phase 4
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Dawnrays Pharmaceutical (Holdings) Limited
Treatments:
Citric Acid
Potassium Citrate
Criteria
Inclusion Criteria:

- Patients with upper urinary tract calculi surgery and/or ESWL within 3 months;

- Stone free or had residual stone fragments with a less than 4 mm diamete;

- 18-70 years of age; the gender is not limited;

- Agree to take effective contraceptive measures during the study period, and female of
childbearing age whose pregnancy test is negative;

- Subjects with no mental illness and language dysfunction, can understand the situation
of the study and have signed informed consent.

Exclusion Criteria:

- Patients with infectious stones, medical stones and urinary tract obstruction;

- Patients with hyperkalemia (K+>5.5mmol/L) (or patients with factors or disease that
can cause hyperkalemia), because the further increase in blood potassium can lead to
cardiac arrest. These factors include disease or strenuous exercise, chronic renal
failure, uncontrolled diabetes, acute dehydration, excessive, adrenal insufficiency,
extensive tissue failure. Patients who takes potassium sparing diuretics (such as
triamterene, spironolactone, amiloride);

- Patients with gastrointestinal disorders, such as peptic ulcer, severe vomiting,
diarrhea, delayed gastric emptying, intestinal obstruction, etc.;

- Combined with cardiovascular, liver, kidney, hematopoietic system, such as severe
primary disease, or known to affect the survival of serious diseases (such as cancer
or AIDS), or patients with with disabilities mentally or legally;

- Patients with renal insufficiency (1.2 times the upper limit of the normal value of
serum creatinine and urea nitrogen);

- The recent (within 6 months) with family planners;

- Allergic to this product;

- To participate in other clinical trials in the past three months.