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The impact of hydronephrosis improvement after ureteroscopy for ureteral stone with edema using Saireito

The impact of hydronephrosis improvement after ureteroscopy for ureteral stone with edema using Saireito - The impact of hydronephrosis improvement after ureteroscopy for ureteral stone with edema using Saireito

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000025437
Enrollment
64
Registered
2017-01-05
Start date
2017-01-05
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Ureteral stone

Interventions

Take Saireito orally Not to be taken internally

Sponsors

Kansai Medical University, Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with ureteral stone and hydronephrosis before transurethral ureterolithotripsy (TUL)

Exclusion criteria

Exclusion criteria: 1)Patients treated bilateral upper tract stone at one stage procedure 2)Patients with thinning of the kidney 3)Patients emerges febrile urinary tract infection after procedure 4)Difficulty of communication 5)When doctor had judged the patients need stent for a long time 6)When doctor had judged the patients disqualified as a subject of this study

Design outcomes

Primary

MeasureTime frame
Comparison with the ratio of the area in hydronephrosis to the area of kidney in the largest cross-sectional slice using ultrasonography between two groups.

Secondary

MeasureTime frame
1)Comparison with stent related pain on stent removal between two groups 2)Comparison with grade of hydronephrosis between two groups 3)Comparison with psychological well-being on stent removal between two groups 4)Comparison with OABSS(Overactive bladder symptom score) and IPSS(International Prostate Symptom Score)on stent removal between two groups 5)Comparison with quantity and frequency of analgestic drug on stent removal between two groups 6)Comparison with complication between two groups

Countries

Japan

Contacts

Public ContactJunichi Ikeda

Kansai Medical University, Medical Center Urology

ikedaj@hirakata.kmu.ac.jp81-6-6992-1001

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026