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NCT06902467Recruiting

Combined Intraperitoneal Chemotherapy Regimen After Optimal Interval Surgery in Advanced Ovarian Cancer: BICOV-1 (Bidirectional Chemotherapy in Ovarian Cancer)

Source: ClinicalTrials.gov · Last updated 30 Mar 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

A multicenter, low-intervention, drug-based study to evaluate the feasibility and safety of a combined regimen of two intraperitoneal chemotherapy modalities (used in routine clinical practice) following interval surgery for the treatment of advanced ovarian cancer. This is an independent research project (free of commercial interests).

Status (registry)
Recruiting
Study type
Interventional
Enrollment
20 (estimated)
First submitted
24 Mar 2025
Start date
27 Feb 2023
Primary completion date
15 Mar 2026
Lead sponsor
Fundacion para la Formacion e Investigacion Sanitarias de la Region de Murcia
NCT number
NCT06902467

What you commit to

  • Study type: Interventional
  • Planned participants: 20
  • From 27 Feb 2023 to the primary completion date, 15 Mar 2026
  • 1 site in 1 country
  • 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

  • Disease progression during systemic treatment with neoadjuvant chemotherapy.
  • Allogeneic transplant, or prior bone marrow transplant, or high-dose chemotherapy with bone marrow or stem cell rescue.
  • Participation in a clinical trial with an investigational drug within the last 30 days.
  • Pregnant or breastfeeding women, where pregnancy is defined as the state of a woman after conception and until the end of pregnancy, confirmed by a positive human chorionic gonadotropin (hCG) test result, or who plan to become pregnant or breastfeed during study treatment or within 30 days of the end of treatment with the study drug.

Other illness

  • Extraperitoneal disease (including retroperitoneal lymph node metastases)
  • Performance of at least one digestive anastomosis of any type. Active infection of any origin
  • Patients with a history of allergic reactions or hypersensitivity to drugs chemically related to cisplatin and paclitaxel.
  • Failure to sign written informed consent.

Other

  • Inability to achieve complete cytoreduction (CC-0) during preoperative (imaging) or intraoperative evaluation.

Who the study is looking for

  • Women aged 18-70 years with a histologically proven diagnosis of FIGO stage IIIB-C/IV epithelial ovarian cancer (high-grade serous epithelial carcinoma)
  • Absence of extraperitoneal disease.
  • Good performance status: Karnofsky score \>70 or Performance status \<= 2
  • Adequate liver function, defined as bilirubin \<0.15 times the upper limit of normal (ULN), aspartate aminotransferase and alanine aminotransferase \<= 2.5 times ULN, and alkaline phosphatase \<= 3 times ULN.
  • Adequate renal function, defined as serum creatinine \<= 1.5 times ULN
  • Acceptable bone marrow function, defined as neutrophils \>1.5 x 106 L-1, hemoglobin \>10 g/dL-1, and platelets \>100.0 x 109 L-1
  • Absence of cardiac, pulmonary, hepatic, renal, or neurological disease that contraindicates major surgery.
  • Negative serum and urine pregnancy test results for women of childbearing potential at the screening visit.
  • Administration of neoadjuvant chemotherapy with a total of 3 or 4 systemic cycles.
  • Surgery with complete CC0 cytoreduction without digestive anastomoses.
  • Patients who have signed the written IC.

Age in the registry: 18 years to 70 years · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
HCUVA
Coordinator of this site? Confirm its status
MurciaSpainRecruiting

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