Prostate cancer / Lymphadenectomy C61
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients with prostate cancer 2. Robot-assisted radical prostatectomy (RALP) possible 3. Simultaneous lymphadenectomy 4. Capable of giving consent, willing to give consent
Exclusion criteria
Exclusion criteria: 1. Multimodal therapeutic concept 2. No consent 3. Individual decision by the patient and/or surgeon not to perform/have lymphadenectomy performed as part of RALP 4. Contraindication to LAD
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| -Number of lymphoceles (in [ml]) collected in the small pelvis postoperatively (day 5-7). | — |
Secondary
| Measure | Time frame |
|---|---|
| -Lymphoceles (in [ml]) at follow-up due to side effects/complications directly/indirectly related to the operation, as well as planned follow-up within the first year after surgery (no study-related visits) -Quality of life (QoL, SF-12 questionnaire) postoperatively (days 5- 7) -Pain perception (VAS pain scale) postoperatively (days 1, 2, 3 and upon discharge) -Drainage duration (in days) and drainage volume (in [ml]) during hospitalisation until final drainage removal -Association of lymphoceles with possible risk factors (number of lymph nodes removed, body mass index, anti-hormonal therapy, previous inguinal hernia repair, etc.) -Length of hospital stay (in days) -Type and number of side effects/complications and development of symptomatic lymphoceles during the inpatient stay and at follow-up within the first postoperative year | — |
Countries
Germany
Contacts
Klinik für Urologie Universitätsmedizin Göttingen