Calcium Electroporation for Urinary Bladder Tumors: A First-in-Human Feasibility, Safety, and Early Response Trial
Starting soon · Phase 1
Conditions studied: Bladder Tumors, Bladder Tumor, Urothelial Carcinoma (UC), Urothelial Carcinoma Bladder
In brief
This phase I study evaluates intravesical calcium electroporation (CaEP) with a new transurethral electrode. The study is primarily designed to assess the safety of CaEP and secondarily, to preliminary explore the efficacy in patients with limited alternative therapies. The anticipated benefits and structured safety precautions justify the ethical conduct of the investigation.
Key facts
- Study ID
- NCT07555769
- Run by
- Juan Luis Vásquez
- People needed
- 20
- Starts
- 2026-06-01
- Expected to finish
- 2030-04-01
- Last updated by the study team
- 2026-04-29
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Age ≥ 18 years and able to understand participant information and give informed consent
- Histologically verified urothelial bladder tumor
- Unfit for cystectomy and/or radiotherapy
- Patients with recurrence after radiotherapy unfit for salvage cystectomy
- Disease where other treatments are considered unsuitable or have been declined by the patient
- The patient may receive simultaneous systemic treatment
- Selected high-burden non-muscle-invasive bladder tumors after MDT assessment
- Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) ≤ 2
- Life expectancy of ≥ 3 months
- Patients must be deemed able to tolerate general anesthesia
- Sexually active participants in the reproductive age must use contraception. Accepted contraception includes the use of intrauterine device (IUD), oral contraceptives, male or female condom, vasectomy or female sterilization
- Patients must stop treatment with anticoagulants before surgery in accordance with national guidelines
- Plasma ionized Ca2+ must be within the normal upper limit. Correction is allowed
- Hematology
- Thrombocytes ≥ 50 billion/L
- International normalized ratio (INR) ≤ 1.5. Correction is allowed
You may not qualify if…
- Pregnancy (confirmed by a blood sample) or lactation
- Allergy to calcium gluconate or any of its excipients
- Any clinical condition or previous treatment, that in the investigators' opinion made the patient ineligible
- Contraindications to treatment with calcium gluconate as described:
- Hypersensitivity to calcium gluconate or any of its excipients
- Hypercalcemia (e.g. due to hyperparathyroidism, hypervitaminosis D, decalcifying malignancies, renal insufficiency, immobilization osteoporosis, sarcoidosis, milk-alkali syndrome)
Full record on ClinicalTrials.gov
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