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Miglitol in the treatment of bladder cancer

Clinical trail for miglitol in the treatment of bladder cancer recurrence and progression

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900027770
Enrollment
Unknown
Registered
2019-11-28
Start date
2020-01-01
Completion date
Unknown
Last updated
2019-12-10

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

Conditions

Bladder Carcinoma

Interventions

single-arm:1
single-arm:2

Sponsors

Shenzhen Luohu People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Initial diagnosis, middle-high-risk urothelial carcinoma patients undergoing transurethral resection or neoadjuvant chemotherapy before electrification; 2. Life expectancy is greater than 5 years and above; 3. Immunohistochemistry confirmed the high expression of a-glucosidase 2; 4. After the communication, I am willing to participate in this test, promise to take the medicine according to the doctor's advice, and can follow up and communicate in time.

Exclusion criteria

Exclusion criteria: 1. Any of the following conditions: those with immunodeficiency or damage (such as AIDS patients) who are using immunosuppressive drugs or radiation therapy; those with fever and acute infectious diseases, including active tuberculosis, or receiving anti-tuberculosis Therapist; accompanied by severe chronic cardiovascular or cerebrovascular disease or chronic kidney disease; 2, combined with other cancer patients; 3. Those who have received chemotherapy, radiotherapy or immunotherapy in the past 4 weeks (except for intravesical infusion chemotherapy immediately after surgery); 4. Known or suspected bladder perforation during surgery; 5. severe urethral stricture can not be placed into the cystoscope; 6. pelvic CT examination or full physical examination found tumor metastasis; 7. Low immune function, acquired, congenital immunodeficiency disease, or history of organ transplantation; 8. suffering from severe cardiovascular and cerebrovascular diseases, such as myocardial infarction, severe / unstable angina, coronary / peripheral artery bypass surgery, symptomatic congestive heart failure, cerebrovascular accident or transient ischemic attack, or pulmonary embolism Those who cannot tolerate TURBT surgery; 9. there are obvious major internal organ dysfunction, such as: creatinine > 1.5 times the upper limit of the normal range, AST, ALT, total bilirubin > 1.5 times the upper limit of the normal range; 10. The fever temperature exceeds 38 degree C, and there are obvious active infections that can affect clinical trials such as acute pneumonia, active tuberculosis, and subjects with severe urinary tract infections; 11. Opioids or alcohol dependent individuals are known; 12. Apparent gastrointestinal reactions after taking miglitol; 13. The investigator believes that there may be any situation that increases the risk of the subject or interferes with the performance of the clinical trial.

Design outcomes

Primary

MeasureTime frame
Recurrence rathe;Relapse free survival;

Countries

China

Contacts

Public ContactWu Song

Shenzhen Luohu People's Hospital (Shenzhen University Third Affiliated Hospital)

wusong@szu.edu.cn+86 18823451804

Outcome results

None listed

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