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Active, not recruiting Not applicable Interventional

Retroperitoneal Lymph Node Dissection in Treating Patients With Testicular Seminoma

ClinicalTrials.gov ID: NCT02537548

Public ClinicalTrials.gov record NCT02537548. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 28, 2026, 9:18 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Surgery in Early Metastatic Seminoma (SEMS): Phase II Trial of Retroperitoneal Lymph Node Dissection as First-Line Treatment for Testicular Seminoma With Isolated Retroperitoneal Disease (1-3cm)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This phase II trial studies how well retroperitoneal lymph node dissection (RPLND) works in treating patients with stage I-IIa testicular seminoma. The retroperitoneum is the space in the body behind the intestines that is typically the first place that seminoma spreads. RPLND is a surgery that removes lymph nodes in this area to treat testicular seminoma and may experience fewer long-term toxicities, such as a second cancer, cardiovascular disease, metabolic syndrome (pre-diabetes), or lung disease.

Study identification

NCT ID
NCT02537548
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Not applicable
Enrollment
55 participants

Conditions and interventions

Eligibility (public fields only)

Age range
16 Years and older
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 28, 2015 (Actual)
Primary completion
Dec 31, 2026 (Estimated)
Completion
Dec 31, 2027 (Estimated)
Last update posted
Jun 9, 2026

2015 – 2027

United States locations

U.S. sites
14
U.S. states
11
U.S. cities
14
Facility City State ZIP Site status
Loma Linda University Medical Center Loma Linda California 92350 —
USC / Norris Comprehensive Cancer Center Los Angeles California 90033 —
University of California, San Francisco San Francisco California 94143 —
Stanford University Hospitals & Clinics Stanford California 94305 —
University of Colorado Hospital - Aurora Aurora Colorado 80045 —
Emory University Atlanta Georgia 30322 —
University of Chicago Medical Center Chicago Illinois 60637 —
Indiana University Indianapolis Indiana 46202 —
Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins Baltimore Maryland 21205 —
Mayo Clinic Rochester Minnesota 55905 —
Rutgers Cancer Institute of New Jersey New Brunswick New Jersey 08903-2681 —
Stephenson Cancer Center, University of Oklahoma Oklahoma City Oklahoma 73104 —
UTSouthwestern Medical Center Dallas Texas 75390-9110 —
Madigan Army Medical Center Tacoma Washington 98431 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02537548, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 9, 2026 · Synced Oct 28, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02537548 live on ClinicalTrials.gov.

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