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Recruiting NCT07498959

NCT07498959 Primary RPLND Versus Systemic Chemotherapy in Good-prognosis Metastatic Testicular Cancer

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Clinical Trial Summary
NCT ID NCT07498959
Status Recruiting
Phase
Sponsor Sahlgrenska University Hospital
Condition Testicular Cancer
Study Type INTERVENTIONAL
Enrollment 160 participants
Start Date 2026-03-19
Primary Completion 2031-03-25

Eligibility & Interventions

Sex Male only
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
primary RPLND for low-stage metasatatic seminoma3 courses of chemotherapy; Blemocin, Etoposide and Platinum (BEP)

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

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 160 participants in total. It began in 2026-03-19 with a primary completion date of 2031-03-25.

⚠ 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 prospective observational study is to learn about the short- and long-term effects of treating men over the age of 18 with good prognosis metastatic testicular cancer with either primary retropertioneal lymph node dissection, RPLND, (for low-stage metastastic seminoma) or three doses of chemotherapy for metastastic seminoma or nonseminoma. The main question it aims to answer is: Does primary RPLND lower the risk of side-effects compared to receiving chemotherapy?

Eligibility Criteria

Inclusion Criteria: * Patients ≥18 years undergoing an open or minimally invasive primary retroperitoneal lymph node dissection (RPLND) due to seminoma stage II A/B (maximum 2 nodes, \<30 mm in any dimension) * Patients undergoing an open or minimally invasive primary RPLND due to a retroperitoneal relapse of seminoma (maximum 2 nodes, \<30 mm in any dimension) * Patients ≥18 years scheduled for 3-4 courses of chemotherapy due to a newly diagnosed good-prognosis metastatic germ cell tumor (nonseminoma or seminoma) Exclusion Criteria: * Previous chemotherapy (including adjuvant chemotherapy at diagnosis) * Previous RPLND * Practical considerations, such as not being able to read and sign informed consent or understand the questionnaires

Frequently Asked Questions

Who can join the NCT07498959 clinical trial?

This trial is open to male participants only, aged 18 Years or older, studying Testicular Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07498959 currently recruiting?

Yes, NCT07498959 is actively recruiting participants. Visit ClinicalTrials.gov or contact Sahlgrenska University Hospital to inquire about joining.

Where is the NCT07498959 trial being conducted?

This trial is being conducted at Gothenburg, Sweden.

Who is sponsoring the NCT07498959 clinical trial?

NCT07498959 is sponsored by Sahlgrenska University Hospital. The trial plans to enroll 160 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology