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NCT04402333: MIRRORS

Minimally Invasive Robotic Surgery, Role in Optimal Debulking Ovarian Cancer, Recovery & Survival

Status unknown Last updated 2 September 2020
What this trial tests

trial testing Robotic Interval Debulking Surgery in Ovarian Cancer in 40 participants. Status unknown.

Timeline
26 June 2020
Primary endpoint
3 October 2021
3 October 2021

Quick facts

Lead sponsorRoyal Surrey County Hospital NHS Foundation Trust
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment40
Start date26 June 2020
Primary completion3 October 2021
Estimated completion3 October 2021
Sites1 location across United Kingdom

Drugs / interventions tested

Conditions studied

Sponsor

Royal Surrey County Hospital NHS Foundation Trust

Who can join

18 and older, female only, with Ovarian Cancer or Ovarian Neoplasm. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

MIRRORS "Minimally Invasive Robotic Surgery, Role in Optimal Debulking Ovarian Cancer, Recovery \& Survival" is a new United Kingdom based prospective feasibility study the purpose of which is to establish the feasibility of launching a British multicentre randomised control trial of Robotic interval debulking surgery for ovarian cancer (including cancer of the fallopian tube \& peritoneum) in the future. This initial feasibility study will focus on the ability to recruit patients, acceptability, quality of life, the rate at which it is possible to remove all visible tumour and the rate of conversion to open surgery. Ultimately the investigators would like to determine whether, in selected patients, robotic surgery offers improved quality of life and recovery with equivalent overall and progression free survival. Robotic surgery is unlikely to be suitable in all cases of ovarian cancer, particularly those with large pelvic masses or extensive disease around the upper part of the abdomen, however, it has the potential to provide significant recovery and quality of life benefits to a selected group of patients. MIRRORS - ICG "Peritoneal angiography / perfusion assessment using Indocyanine green (ICG) in patients with advanced ovarian cancers" is a ancillary study within MIRRORS. Using ICG dye, the investigators aim to observe whether there are any changes in the blood vessel pattern associated with the tumour deposits the investigators remove that makes them distinctive. The ICG will not be used to guide where biopsies are taken or tissue is removed. Participation in this ancillary research is not required for participation in the trial.

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

  1. MIRRORS ICG: Perfusion Assessment Using Indocyanine Green (ICG) Peritoneal Angiography during Robotic Interval Cytoreductive Surgery for Advanced Ovarian Cancer.
    Uwins C, Michael A, Skene SS, Patel H, et al · · 2024 · cited 3× · PMID 39123417 · DOI 10.3390/cancers16152689
  2. Minimally invasive surgery in gynecologic oncology: a narrative review of controversies and clinical implications.
    Ayoub NL, Shin R, Tseng J, Francoeur AA. · · 2025 · PMID 42211936 · DOI 10.21037/gpm-25-19

Verify or expand the search:

Other recruiting trials for Ovarian Cancer

Currently open trials in the same condition.

Other Royal Surrey County Hospital NHS Foundation Trust trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04402333.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing