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Clinical Trials in Germany / NCT04269512
Active, not recruiting Not applicable

Role of Lymphnode Dissection in Men With Prostate Cancer Treated With Radical Prostatectomy

NCT04269512 · tracked via the Priya Life Science Germany tracker
Phase
Not applicable
Started
2019-10-15
Last updated
2026-01-12

Condition(s) studied

Prostate Cancer

Investigational drug(s) / intervention(s)

lymph node dissection

lymph node dissection: At least 10 lymph nodes must be removed.

Study summary

Currently, lymph node dissection is standard of care during prostatectomy of intermediate risk tumors at the Martini Clinic. It allows the assessment of possible but unlikely lymph nodes metastases. In case of lymph node metastasis, depending on the number of affected lymph nodes, an adjuvant radiation with or without additional hormone therapy may be discussed in order to stop or delay further progression of the disease.

Since the procedure carries additional risks, it is controversial. The risks include prolonged surgery duration, injury of vessels and nerves, as well as disorders of lymphatic circulation after surgery. Moreover, formation of lymphoceles (accumulation of lymph fluid in the tissue) are common, which may result in soft tissue swelling, thrombosis, inflammation and additional surgical procedures.

Therefore, the aim of this study is to evaluate whether the removal of the lymph nodes during prostatectomy positively influences the course of the disease in patients with intermediate risk prostate cancer, or if the lymph node dissection does not have any influence on the recurrence of the disease and therefore further therapies.

In this case, the omission of lymph node dissection may avoid an unnecessary expansion of the operation and the potentially associated side effects linked to it. This is particularly of interest considering the rapidly advancing technical possibilities, both in imaging and in the treatment of prostate cancer, since this enables an earlier and more individual intervention in the case of recurrence.

Eligibility

Sex
MALE
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: * localized intermediate risk prostate cancer (intermediate risk (PSA\> 10 ng / ml - 20 ng / ml or Gleason score 7 or cT category 2b) * scheduled for open radical prostatectomie or DaVinci prostatectomie Exclusion Criteria: * American Society of Anesthesiology Classification\> 3 * Existing contraindications for performing a lymph node dissection * Neoadjuvant hormone therapy

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Martini-Klinik am UKE GmbH Hamburg Germany

More Martini-Klinik am UKE GmbH trials in Germany

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 NCT04269512 on ClinicalTrials.gov ↗ ← All trials in Germany