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A clinical trial of Desmodium styracifolium total flavone capsule in the treatment of urinary calculi (Damp-heat accumulation)

Desmodium styracifolium total flavone capsule in the treatment of urinary calculi (Damp-heat accumulation): A random, double blind, parallel controlled clinical trial of efficacy and safety

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-12002583
Enrollment
Unknown
Registered
2012-09-20
Start date
2012-07-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

urinary stone disease(Shireyunjie-category)

Interventions

High dose group:high dose Desmodium styracifolium total flavone capsule
midle dose group:midle dose Desmodium styracifolium total flavone capsule
Low dose group:low dose Desmodium styracifolium total flavone capsule

Sponsors

People's Hospital Affiliated to Fujian University of TMC
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Stone in the renal pelvis or ureter stone; (2) Male and female aged 18 to 65 years old; (3) Stone diameter: 0.4cm< diameter<=l.0cm; (4) Renal function is good, especially the ipsilateral renal function is good, if the patients have kidney ponding, the degree of hydronephrosis in moderate following; (5) General condition is good, life can take care of themselves; (6) Signed informed consent form.

Exclusion criteria

Exclusion criteria: (1) Kidney, ureter junction, or distal ureteral calculi with malformations, stenosis, obstruction and operation scar adhesion; (2) severe hydronephrosis (grade III); (3) sustained severe hematuria, or even shock; (4) acute obstructive oliguria, anuria; (5) during pregnancy, breastfeeding women; (6) with cardiovascular, hepatic, renal, hematopoietic system of severe primary disease, or to affect the survival of the serious diseases (such as cancer or AIDS), or mental or legally disabled patients; (7) the liver function ALT and/or AST values in normal values outside; (8) a month over the use of surgical intervention in the treatment of urolithiasis; (9) on the basis of judgment, can reduce the likelihood or make into the group into the group of complex of other lesions, such as work environment often change is easy to cause the loss of follow up; (10) within the past three months, participated in drug clinical trials; (11) known to the drugs or their composition allergy.

Design outcomes

Primary

MeasureTime frame
Stone does exclude;

Countries

China

Contacts

Public ContactZhou Hao
haookok@qq.com+86 18959117277

Outcome results

None listed

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