Ireland
--:--IST
Latest
Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: Trade Data, Destination Markets, and Economic Impact Astellas Expands Its 330 Million Euro Tralee Biopharma Facility with a Second Aseptic Filling Line to Double Drug-Product Capacity Xeolas Pharmaceuticals Opens 158,000 Sq Ft State-of-the-Art Baldoyle Facility to Scale Specialty Medicine Manufacturing Priya Life Science Partners with Fleming for the 9th Annual Corporate Compliance & Transparency in Life Sciences Summit in Zurich Ireland Has the Capital and the Lessons: Digital Project Management Is How They Become Delivery Dunbar Pharma Brings First Plant-Derived Dronabinol API to UK Market Through IPS Pharma Leveraging Priya Life Science as a Data Tracker: The Ultimate Use Case & Career Guide The €100K Reality Check: Why a Six-Figure Pharma Salary in Ireland Feels Different Than in Switzerland or Germany Ireland's €93.8 Billion Non-EU Pharma Export Engine: Trade Data, Destination Markets, and Economic Impact
Clinical Trials in the Netherlands / NCT05076942
Recruiting Phase 2

Groningen International Study on Sentinel Nodes in Vulvar Cancer-III

NCT05076942 · tracked via the Priya Life Science Netherlands tracker
Phase
Phase 2
Started
2021-01-01
Last updated
2023-08-01

Condition(s) studied

Vulvar CancerSentinel Lymph NodeLymph Node Metastases

Investigational drug(s) / intervention(s)

Radiotherapy combined with cisplatinCisplatin →

Radiotherapy combined with cisplatin: Inguinofemoral radiotherapy combined with weekly cisplatin

Cisplatin: Inguinofemoral radiotherapy combined with weekly cisplatin

Study summary

Vulvar cancer patients with SN-metastasis \> 2mm will receive chemoradiation instead of an inguinofemoral lymphadenectomy.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Histological confirmed primary SCC of the vulva * T1 tumor, not encroaching urethra/vagina/anus * Depth of invasion \> 1mm * Tumor diameter \< 4cm * Unifocal tumor * No enlarged (\>1.5cm) or suspicious inguinofemoral lymph nodes at imaging (CT/MRI/ultrasound) * Possibility to obtain informed consent * Metastatic sentinel lymph node; size of metastasis \> 2mm and / or extracapsular extension, or * Metastatic sentinel lymph node: more than 1 SN with metastasis ≤ 2mm * Patients are able to understand requirements of study, provide written informed consent and comply with the study and follow-up procedures * Adequate bone marrow, renal and liver function: * Absolute neutrophil count ≥ 1.5 x 109 /L * Platelet count ≥ 100 x 109 /L * Creatinine clearance ≥ 40 ml/min measured by the Cockroft Gault formula * Total bilirubin \< 1.25 x ULN Aspartate transaminase (AST) and alanine transaminase (ALT) ≤ 2.5 x ULN * Performance status of 0, 1 or 2 on the Eastern Cooperative Oncology Group (ECOG) Scale (Appendix A) * Age 18 years or older * Life expectancy of ≥ 12 weeks * Written informed consent Exclusion Criteria: * Inoperable tumors and tumors \> 4cm * Multifocal tumors * Tumors with other pathology than squamous cell carcinoma * Patients with enlarged / suspicious lymph nodes which are proven metastatic after fine needle aspiration cytology * No other carcinomas, other than basal cell carcinomas, within last 5 years * History of pelvic radiotherapy * History of any infection requiring hospitalization or antibiotics within 2 weeks before enrollment * Pregnant female or nursing mother * Desire to become pregnant * Known brain or spinal cord metastases unless adequately treated (surgery or radiotherapy) with no evidence of progression and neurologically stable off anticonvulsants and steroids * Unstable angina, myocardial infarction, cerebrovascular accident, \> Class II congestive heart failure according to the New York Heart Association Classification for Congestive Heart Failure (see Appendix B) within 6 months before enrollment

Primary outcome measure(s)

Trial sites (27)

FacilityCityRegionStatus
UC Irvine Health/Chao Family Comprehensive Cancer Center Orange California Recruiting
Mount Sinai Medical Center Miami Beach Florida Recruiting
Baystate Medical Center Springfield Massachusetts Recruiting
Spectrum Health at Butterworth Campus Grand Rapids Michigan Recruiting
Munson Medical Center Traverse City Michigan Recruiting
Nebraska Methodist Hospital Omaha Nebraska Recruiting
Women's Cancer Center of Nevada Las Vegas Nevada Recruiting
Memorial Sloan Kettering Basking Ridge Basking Ridge New Jersey Recruiting
Memorial Sloan Kettering Monmouth Middletown New Jersey Recruiting
Memorial Sloan Kettering Bergen Montvale New Jersey Recruiting
Memorial Sloan Kettering Commack Commack New York Recruiting
Memorial Sloan Kettering Westchester Harrison New York Recruiting
Memorial Sloan Kettering Cancer Center New York New York Recruiting
Memorial Sloan Kettering Nassau Uniondale New York Recruiting
Duke University Medical Center Durham North Carolina Recruiting
Duke Women's Cancer Care Raleigh Raleigh North Carolina Recruiting
Ohio State University Comprehensive Cancer Center Columbus Ohio Recruiting
ProMedica Flower Hospital Sylvania Ohio Recruiting
University of Oklahoma Health Sciences Center Oklahoma City Oklahoma Recruiting
Women and Infants Hospital Providence Rhode Island Recruiting
Avera Cancer Institute Sioux Falls South Dakota Recruiting
Catharina Hospital Eindhoven Eindhoven Netherlands Recruiting
University Medical Center Groningen Groningen Netherlands Recruiting
Leiden University Medical Center Leiden Netherlands Recruiting
Radboud University Medical Center Nijmegen Netherlands Recruiting
Erasmus Medical Center Rotterdam Netherlands Recruiting
University Medical Center Utrecht Utrecht Netherlands Recruiting

More University Medical Center Groningen trials in the Netherlands

Other trials for the same condition

Official registry record

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

View NCT05076942 on ClinicalTrials.gov ↗ ← All trials in the Netherlands