NCT06839144RecruitingPhase 2
Inhibiting Beta-adrenergic and COX-2 Signaling During the Perioperative Period to Reduce Ovarian Cancer Progression
Inhibiting Beta-adrenergic and COX-2 Signaling During the Perioperative Period to Reduce Ovarian Cancer Progression: A Randomized Placebo-Controlled Clinical Trial
Source: ClinicalTrials.gov · Last updated 11 Jul 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
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.
- Status (registry)
- Recruiting
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 60 (estimated)
- First submitted
- 6 Feb 2025
- Start date
- 12 Mar 2025
- Primary completion date
- 31 Aug 2026
- Lead sponsor
- Tel-Aviv Sourasky Medical Center
- Diseases
- Ovarian cancer
- NCT number
- NCT06839144
What you commit to
- Study type: Interventional · Phase 2
- Planned participants: 60
- From 12 Mar 2025 to the primary completion date, 31 Aug 2026
- 2 sites 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
- 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
- Recent (within the last 5 years) or concurrent malignancies, with the exception of adequately treated in-situ carcinoma of the cervix or basal-cell carcinoma of the skin
- Patients who are treated with immunosuppressive medications, including chronic systemic steroid therapy (in dosing exceeding 10 mg daily of prednisone equivalent) or any other form of immunosuppressive therapy within 7 days prior to the first dose of trial drug
Other illness
- 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 with active peptic disease
- Patients with a history of CVA/TIA
- Patients with significant heart failure (NYHA functional class 3 or Higher)
- Patients with bradycardia (heart rate of 50 or less) or second- or third-degree AV block
- Patients with right-sided heart failure owing to pulmonary hypertension
- Patients with Printzmetal's angina
- Patients suffering from sick sinus syndrome
- Patients with peripheral vascular disease
- Patients with Immunodeficiency Disorders
Lab values
- Patients with renal failure, measured by creatinine level \>1.5
- Patients with significant liver dysfunction (known cirrhosis, Bilirubin level\>2)
Other
- Patients who participate in another interventional study
- Patients currently suffering from asthma (אסתמה פעילה בלבד), or required hospital admission or change in medical treatment for asthma within the past year
- Patients with chronic Digoxin treatment
- Patients with significant diagnosed cardiomegaly
- Patients with current (unresected) pheochromocytoma
- Pregnant women
Who the study is looking for
- 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
- Signed informed consent form
- Willing and able to comply with study procedures (physically and mentally)
Age in the registry: 20 years to 85 years · Sex: Female · Does not accept healthy volunteers
Sites (2)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| The Chaim Sheba Medical Center Coordinator of this site? Confirm its status | Ramat Gan | Israel | Recruiting |
| Tel Aviv Sourasky Medical Center (Ichilov Hospital) Coordinator of this site? Confirm its status | Tel Aviv | Israel | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.