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Clinical Trials in the EU / 2026-525406-36-00
Authorised Phase II

Hyperthermic Intraperitoneal Chemotherapy and Regional Adrenalectomy in the management of Stage II & III Adrenocortical Carcinoma

2026-525406-36-00 · tracked via the Priya Life Science EU tracker
Sponsor
Azienda Socio Sanitaria Territoriale Degli Spedali Civili Di Brescia
Sponsor type
Hospital/Clinic/Other health care facility
Therapeutic area
Neoplasms
Decision date
02/09/2026
Enrollment target
32
Sites
Italy

Condition studied

Adrenocortical Carcinoma

Investigational medicinal product(s)

THIOSULFATECISPLATINDOXORUBICIN

Eligibility

Age group
65+ years, 18-64 years
Sex
Female, Male

Primary endpoint

The percentage of patients with local or peritoneal disease recurrence within 36 months after surgery.

Endpoint detail

Percentage of patients with major perioperative morbidity (grade > 2 according to the Clavien-Dindo classification of surgical complications)., Postoperative mortality rates at 30 and 90 days., Disease-specific survival up to 3 years after surgery.

Official registry record

This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View 2026-525406-36-00 on CTIS ↗ ← All trials in the EU