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Recruiting NCT06537960

NCT06537960 Interest of Late Images for the Assessment of Extensions in 18FGD PET-CT of Muscle-Invasive Bladder Cancers

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Clinical Trial Summary
NCT ID NCT06537960
Status Recruiting
Phase
Sponsor Hopital Foch
Condition Muscle-Invasive Bladder Carcinoma
Study Type INTERVENTIONAL
Enrollment 66 participants
Start Date 2023-12-14
Primary Completion 2027-03-15

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
18FDG PET-CT

Eligibility Fast-Check

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What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 66 participants in total. It began in 2023-12-14 with a primary completion date of 2027-03-15.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The goal of this study is to demonstrate a significant gain in sensitivity versus surgical curage (extended pelvic) for initial lymph node staging of late FDG-PET images (2.5 hours) versus standard images (1 hour), analyzed by side (right iliac/left iliac areas in Patients with muscle-invasive bladder tumor (MIBT) (≥pT2) referred for FDG-PET in the nuclear medicine department of Hôpital Foch as part of their initial extension workup. Before performing 18FDG PET-CT, the operator checks that the patient has fasted for at least 6 hours and that blood glucose levels are below 11 mmol/l. In the absence of contraindication, intravenous (IV) injection of the radiopharmaceutical (18FDG at a dose of 3 MBq/kg) and a diuretic (Furosemide 20mg) will be performed as part of routine care. The 18FDG PET-CT scan will be performed in 2 phases: 1st phase: Standard acquisition (vertex to mid-thigh) at 1 hour post-injection of radiotracer. PET acquisition is coupled to a "base-dose" CT scan in spontaneous contrast, for anatomical location, measurement of lymph node size, and creation of an attenuation map, necessary for correction of attenuation and diffusion on PET images (DLP estimated at around 500 mGy.cm on average). Micturition is performed as part of routine care just before the first acquisition. Phase 2: Complementary abdomino-pelvic acquisition at 2.5 hours post-injection (2 or 3 steps depending on patient size. This second PET acquisition is coupled to an "ultra-base-dose" CT scan in spontaneous contrast, to be used only for attenuation and diffusion correction (DLP estimated at around 100 mGy.cm on average). Micturition is performed 30 minutes before the second acquisition. The patient's proposed therapeutic management will be decided at the PCR once the extension work-up has been carried out, as part of routine care. For this purpose, only "standard" 18FDG PET-CT images may be used. As a general rule, patients with distant metastases (stage pT2N+M+) will receive palliative treatment, while surgical treatment from the outset, or after chemotherapy for patients with stage pT2N0M0 or pT2N+M0, will be discussed on a case-by-case basis at the multidisciplinary consultation meeting. Late" images will be used after lymph node curage, in patients who have not had chemotherapy prior to surgery (cystectomy + extended pelvic lymph node curage), to determine the sensitivity of these complementary images.

Eligibility Criteria

Inclusion Criteria: * Patient 18 years of age or older, * With histologically proven muscle-invasive bladder cancer (≥pT2) at endoscopic bladder resection, * Scheduled to undergo 18FDG PET-CT in the nuclear medicine department at Hôpital Foch, * Having signed a consent form, * Affiliated to a health insurance scheme. Exclusion Criteria: * Patient with a history of pelvic or genitourinary cancer, * Patient with known metastatic disease, * Patient with a contraindication to 18FDG PET-CT, * Pregnant or breast-feeding woman, * Patient deprived of liberty or under guardianship.

Contact & Investigator

Central Contact

MARC BERTAUX, Dr

✉ drci.promotion@hopital-foch.com

📞 00 33 1 46 25 11 94

Frequently Asked Questions

Who can join the NCT06537960 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Muscle-Invasive Bladder Carcinoma. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06537960 currently recruiting?

Yes, NCT06537960 is actively recruiting participants. Contact the research team at drci.promotion@hopital-foch.com for enrollment information.

Where is the NCT06537960 trial being conducted?

This trial is being conducted at Suresnes, France.

Who is sponsoring the NCT06537960 clinical trial?

NCT06537960 is sponsored by Hopital Foch. The trial plans to enroll 66 participants.

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