The Clinical Research of Traditional Chinese Medicine Formula (NCT07746219) | Clinical Trial Compass
Not Yet RecruitingPhase 4
The Clinical Research of Traditional Chinese Medicine Formula
80 participantsStarted 2026-08-31
Plain-language summary
This study examines the efficacy and safety of Bushen Huoxue Simiao formula for tonifying the kidneys and promoting blood circulation in treating postoperative complications of upper urinary tract stones, thereby providing evidence-based medical evidence and treatment strategies for clinical practice.
Who can participate
Age range
18 Years – 80 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
. Meet the Western medicine diagnostic criteria: Patients who need lithotripsy surgery and have a double J stent (4.7F, 28 cm) placed after surgery; plain film of kidney and upper bladder indicates normal position of ureteral stent and no need for stage II surgery.
. Meet the Traditional Chinese Medicine (TCM) diagnostic criteria.
. Aged between 18 and 80 years old (inclusive).
. Voluntary participation with signed informed consent.
Exclusion criteria
. Patients with renal insufficiency stage 4 or 5, or acute renal failure.
. Secondary factors confirmed by examination, such as systemic lupus erythematosus or drug-induced kidney damage.
. Does not meet the diagnosis of upper urinary tract stones.
. Cases not within the scope of drug action.
. Long-term use of other relevant therapeutic drugs, or inability to stop medication immediately.
. Late-stage deformity, disability, or loss of labor ability.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Urinary System Symptom Questionnaire (USSQ).
Timeframe: Baseline and 4 weeks after treatment
Trial details
NCT IDNCT07746219
SponsorThe Fourth Affiliated Hospital of Zhejiang University School of Medicine