Fact CheckerSign in

NCT02828618Active, not recruiting

Trial on Radical Upfront Surgery in Advanced Ovarian Cancer

Source: ClinicalTrials.gov · Last updated 3 Oct 2025

Brief summary (registry, in English)

This study consists of three parts, whereas Part 1 and Part 2 are performed in Germany only, and Part 3 is a multinational trial. All patients with suspicion of advanced ovarian cancer are detected in the participating study centers in a pre-screening. The study centers will register all patients with suspected ovarian cancer in a screening log. After the patients have given informed consent, they can be enrolled in different parts of the study. TRUST-Trial: This part compares two strategies in the therapy of advanced ovarian cancer. En detail, this part of the trial will evaluate if one of two strategies of timing surgery within the therapeutic procedures may show any significant advances in terms of overall survival over the other.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
797 (actual)
First submitted
30 Jun 2016
Start date
1 Jul 2016
Primary completion date
28 Feb 2025
Lead sponsor
AGO Study Group
NCT number
NCT02828618

What you commit to

  • Study type: Interventional
  • Participants enrolled: 797
  • From 1 Jul 2016 to the primary completion date, 28 Feb 2025
  • 20 sites in 8 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior chemotherapy for ovarian cancer or abdominal/pelvic radiotherapy
  • Clinical relevant dysfunctions of blood clotting (including drug induced)

Other illness

  • Non epithelial ovarian malignancies and borderline tumors
  • Secondary invasive neoplasms in the last 5 years (except synchronal endometrial carcinoma FIGO IA G1/2, non melanoma skin cancer, breast cancer T1 N0 M0 G1/2) or with any signs of relapse or activity.
  • Recurrent ovarian cancer
  • Dementia or significantly altered mental status that would prohibit the understanding and giving of informed consent

Age

  • Any significant medical reasons, age or performance status that will not allow to perform the study procedures (estimation of investigator)

Other

  • Unresectable parenchymal lung metastasis, liver metastasis or bulky lymph-nodes in the mediastinum in CT chest and abdomen/pelvis
  • Pregnancy
  • Any reasons interfering with regular follow-up

Who the study is looking for

  • suspected or histologically confirmed, newly diagnosed invasive epithelial ovarian cancer FIGO stage IIIB-IV (IV only if resectable metastasis)
  • Females aged ≥ 18 years
  • Patients who have given their written informed consent
  • Good performance status (ECOG 0/1)
  • Good ASA score (1/2)
  • Preoperative CA 125/CEA ratio ≥ 25 (if CA-125 is elevated)\*
  • If \<25 and/or biopsy with non-serous, non-endometroid histology, esophago-gastro-duodenoscopy (EGD) and colonoscopy mandatory to exclude gastrointestinal primary cancer
  • Assessment of an experienced surgeon, that based on all available information, the patient can undergo the procedure and the tumor can potentially be completely resected
  • Adequate bone marrow function: Absolute neutrophil count (ANC) ≥ 1.5 x 109/L. This ANC cannot have been induced or supported by granulocyte colony stimulating factors.
  • Platelet count ≥ 100 x 109/L.
  • Renal function: Serum-Creatinine ≤ 1.5 x institutional upper limit normal (ULN).
  • Hepatic function:
    • Bilirubin ≤ 1.5 x ULN.
    • SGOT ≤ 3 x ULN
    • Alkaline phosphatase ≤ 2.5 x ULN.
  • Neurologic function: Neuropathy (sensory and motor) less than or equal to CTCAE Grade 1.

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (20)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Medical University of Vienna
Coordinator of this site? Confirm its status
ViennaAustriaUnknown status
Charité - Universitätsmedizin Berlin, Campus Virchow Klinikum, Klinik für Gynäkologie
Coordinator of this site? Confirm its status
BerlinGermanyUnknown status
Universitätsklinikum Carl Gustav Carus Dresden, Klinik & Poliklinik f. Frauenheilkunde & Geburtshilfe
Coordinator of this site? Confirm its status
DresdenGermanyUnknown status
Kaiserswerther Diakonie; Florence-Nightingale-Hospital
Coordinator of this site? Confirm its status
DüsseldorfGermanyUnknown status
Kliniken Essen-Mitte, Evang. Huyssens-Stiftung, Klinik für Gynäkologie und gyn. Onkologie
Coordinator of this site? Confirm its status
EssenGermanyUnknown status
Universitätsklinikum Hamburg-Eppendorf, Klinik und Poliklinik für Gynäkologie
Coordinator of this site? Confirm its status
HamburgGermanyUnknown status
Klinik und Poliklinik für Frauenheilkunde und Geburtshilfe, Klinikum der Universität München
Coordinator of this site? Confirm its status
MünchenGermanyUnknown status
Klinikum rechts der Isar, Frauen- und Poliklinik
Coordinator of this site? Confirm its status
MünchenGermanyUnknown status
Universitätsklinikum Tübingen
Coordinator of this site? Confirm its status
TübingenGermanyUnknown status
University Hospital, Rigshospitalet
Coordinator of this site? Confirm its status
CopenhagenDenmarkUnknown status
Institut Bergonie
Coordinator of this site? Confirm its status
BordeauxFranceUnknown status
Hôpital Européen Georges Pompidou (HEGP)
Coordinator of this site? Confirm its status
ParisFranceUnknown status
Institute Gustave Roussy
Coordinator of this site? Confirm its status
VillejuifFranceUnknown status
Imperial College London, Hammersmith Hospital, Surgery&Cancer
Coordinator of this site? Confirm its status
LondonUnited KingdomUnknown status
European Institute of Oncology; Gynecologic Cancer Surgery
Coordinator of this site? Confirm its status
MilanItalyUnknown status
Fondazione IRCCS Istituto Nazionale Tumori - Milan
Coordinator of this site? Confirm its status
MilanItalyUnknown status
Istituto Nazionale per lo Studio e la Cura dei Tumori di Napoli
Coordinator of this site? Confirm its status
NaplesItalyUnknown status
Skåne University Hospital
Coordinator of this site? Confirm its status
LundSwedenUnknown status
Karolinska University Hospital
Coordinator of this site? Confirm its status
SolnaSwedenUnknown status
Memorial Sloan-Kettering Cancer Center
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.