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Protocol for a Randomized Controlled Trial on Preventing Recurrence after Urinary Calculus Surgery

Effect of an Enhanced Education Model Based on a "Stone Prevention License" on Preventing Recurrence after Urinary Calculus Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600117794
Enrollment
Unknown
Registered
2026-01-29
Start date
2026-02-02
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Urinary Calculi

Interventions

Control Group:Routine Health Education Follow-up Management
Control Group:Follow-up Examination Requirements: Emphasize the necessity of follow-up examinations. Clearly inform patients that even if asymptomatic, they are advised to return for imaging examinati
Intervention Group:Routine Health Education: Mastery Learning Intervention for 'Kidney Stone Prevention and Treatment License'

Sponsors

Baiyun District Maternity and Child Health Care Hospital, Guangzhou
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1.Aged 18 to 60 years. 2.Hospitalized patients with a first episode of renal or ureteral calculi who have undergone surgical treatment. 3.Postoperative imaging assessment confirms the achievement of Stone-Free Status (SFS). 4.Possess lucid consciousness and are able to cooperate in completing knowledge tests and questionnaires. 5.Have the capability to use a smartphone for WeChat communication. 6.Voluntarily sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1.Have a previous history of urinary calculi (non-first episode) or have received relevant interventions in the past. 2.Have underlying diseases requiring specialized management, such as hyperparathyroidism, cystinuria, etc. 3.Have severe comorbid physical illnesses or a life expectancy of less than 6 months. 4.Are unable to independently cooperate with follow-up procedures. 5.Are deemed by the study physician as unsuitable for increased fluid intake or at significant risk for "high-volume water intake unsuitability." This includes, but is not limited to: Heart failure or significant fluid/sodium retention with lower limb edema; Moderate to severe renal insufficiency (significantly reduced eGFR); A history of hyponatremia, or currently using medications/situations that may affect water-electrolyte balance (e.g., factors related to antidiuretic hormone). Subjects meeting these conditions may be considered for "alert/exclusion," and the rationale for the decision must be documented in the Case Report Form (CRF).

Design outcomes

Primary

MeasureTime frame
24-hour urine collection;

Countries

China

Contacts

Public ContactWang Fengfeng

Baiyun District Maternity and Child Health Care Hospital, Guangzhou

258348215@qq.com+86 20 8625 3940

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 7, 2026