Inhibiting Beta-adrenergic and COX-2 Signaling During the Perioperative Period to Reduce Ovarian Cancer Progression

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexFemale
Age20-85
SponsorTel-Aviv Sourasky Medical Center

About this trial

This study investigates the impact of perioperative inhibition of beta-adrenergic and COX-2 signaling in ovarian cancer patients undergoing debulking surgery. The trial aims to assess the feasibility, safety, and biological effects of a combination of propranolol and etodolac in reducing cancer metastasis and improving immune responses.

Eligibility criteria

Qualifiers

Age 20-85

ASA score 1-3 or ECOG Performance Status of 0 to 2

Patients with a suspected high-grade ovarian epithelial cancer based on imaging, clinical examination, CA125, and/or tumor biopsy

Patients planned for surgery for primary surgery, or interval debulking surgery for ovarian cancer

Disqualifiers

Patients who participate in another interventional study

Patients with known allergy to one or more of the study medications, or to any medication from the non-steroidal anti-inflammatory drug group or beta-blockers family

Patients treated chronically with any type of a beta-adrenergic blocker or a COX inhibitor, except use of Aspirin, which will be discontinued at least 7 days prior to surgery, and until 3 weeks post-surgery

Patients currently suffering from asthma (אסתמה פעילה בלבד), or required hospital admission or change in medical treatment for asthma within the past year

Trial design

Treatments tested in this trial

  • Propranolol (Beta-Blocker) and Etodolac (COX-2 Inhibitor)
  • Placebo (Matching for Propranolol & Etodolac)

Treatment groups

60 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Tel-Aviv Sourasky Medical Center

Lead sponsor

National Cancer Institute (NCI)

Collaborator

The Chaim Sheba Medical Center

Collaborator