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Clinical effectiveness of modified single pigtail fishtail stent on preoperative stenting and postoperative stenting during flexible ureteroscopic lithotripsy

Clinical effectiveness of modified single pigtail fishtail stent on preoperative stenting and postoperative stenting during flexible ureteroscopic lithotripsy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300069102
Enrollment
Unknown
Registered
2023-03-07
Start date
2022-04-15
Completion date
Unknown
Last updated
2023-05-22

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

Conditions

ureteral calculus

Interventions

Experiment group:The ureteral stent was modified
Control group:Conventional ureteral stent

Sponsors

Medical Ethics Committee of Quzhou People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Patient aged between 18-80 years, with unilateral upper ureteral calculi or renal calculi complicated with hydronephrosis confirmed by imaging examination, the maximum diameter of calculi<2cm; (2) The body tolerated the operation without cardiopulmonary dysfunction, abnormal coagulation function, uncontrolled infection and other surgical contraindications; (3) All patients had unilateral indwelling double pigtail ureteral stents, and no double pigtail ureteral stents had been indwelled in the past. (4) Abdominal plain films were taken 2 weeks after surgery to confirm the normal position of the double J stent tubes and exclude large residual stones. (5) All patients signed informed consent.

Exclusion criteria

Exclusion criteria: (1) Patients with definite ureteral malformation or ureteral stricture; (2) Patients with urologic tumors; (3) Patients with severe hepatic and renal insufficiency or uremia; (4) Had severe lower urinary tract symptoms in the past or a history of overactive bladder syndrome(OAB) (5) There has diseases such as bladder outlet obstruction, urinary retention, neurogenic voiding dysfunction, stress urinary incontinence, severe gynecological infection and gynecological tumors;

Design outcomes

Primary

MeasureTime frame
ureteral stent symptoms questionnaire (USSQ);

Secondary

MeasureTime frame
postoperative complications;

Countries

china

Contacts

Public ContactLijun Wan

Quzhou People's Hospital

qzrymnwk@163.com+86 15657009012

Outcome results

None listed

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