Under construction – not a live service
Sign in
Taking people in TürkiyeNo phase

Checks a score for choosing surgery first in advanced ovarian cancer

Studies a scoring tool to predict surgery outcomes in adults with advanced ovarian cancer.

Key facts

Who runs it
Cukurova University
Where
Adana, TürkiyeSee the site
Trial code
Registry title
Cukurova Score Validation Study
Status
Recruiting
People taking part
130 people, planned
Started
30 May 2024
Expected to end
Mar 2027
Type of study
Observational
Record updated
29 August 2024

Who can take part

AI summary

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for adult women with advanced epithelial ovarian, fallopian tube or primary peritoneal cancer. It checks whether the Cukurova score predicts the result of primary cytoreduction surgery.

Age
18 years and over (up to 100 years)
Sex
Women
Disease stage
Stage III-IV epithelial ovarian, fallopian tube or primary peritoneal cancer, confirmed by pathology; advanced disease suspected on imaging

Main reasons for not taking part

  • Stage I-II epithelial ovarian, fallopian tube or peritoneal cancer
  • Non-epithelial ovarian cancer
  • Benign or borderline ovarian tumors
  • Metastatic ovarian tumors
  • Under 18 years old or not agreeing to take part

The registry criteria, word for word

Show all 11 criteriaShow less

Who can take part

  • 18 years old and over
  • Suspected advanced ovarian/fallopian tube/ primary peritoneal carcinomatosis on imaging
  • Pathologically confirmed Stage III-IV epithelial ovarian cancer/fallopian tube/ primary peritoneal carcinomatosis
  • Consent to participate in the study

Who cannot take part

  • Stage I-II epithelial ovarian/fallopian tube/peritoneal cancer
  • Nonepithelial Ovarian Cancer
  • <18 years old
  • Benign Ovarian tumors
  • Borderline Ovarian Tumors
  • Metastatic Ovarian Tumors
  • Rejecting to Participate in the Study

Check if you might fit

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 100 years old?

Where in Türkiye

  • Cukurova UniversityAdana, TürkiyeContact: Ghanim Khatib, MDTaking people

About the trial

What the trial wants to find out

Despite significant advancements in imaging technologies, surgical techniques, chemotherapeutic regimens, and treatment strategies in recent years, ovarian cancer continues to remain the most deadly gynecological malignancy. Approximately 90% of ovarian cancers originate from the coelomic epithelium or modified mesothelial cells and are classified as epithelial ovarian cancers. The majority of patients with epithelial ovarian cancer (70-80%) present in advanced stages. The primary treatment for advanced-stage (stage 3-4) disease consists of primary cytoreductive surgery followed by adjuvant chemotherapy. Cytoreductive surgery aims to remove all visible tumor implants regardless of the extent of the disease and achieve no visible residual tumor (complete cytoreduction, R0) at the end of the surgery. In cases where R0 cannot be achieved (due to poor general condition and/or extensive tumor that cannot be completely excised surgically), the option of neoadjuvant chemotherapy followed by interval cytoreductive surgery is considered. Primary cytoreductive surgery is still the preferred option and is considered a quality indicator for centers performing advanced-stage ovarian cancer surgeries. Despite advancements in surgery, the decision for interval surgery following primary surgery or neoadjuvant chemotherapy is often based on the surgeon's experience, imaging results, and clinic preferences. Various methods and scores have been published and applied to predict which patients are suitable for primary surgery.

Read full original descriptionShow less

The Cukurova score developed in our clinic conceptualizes prioritizing surgical procedures using radiological imaging and diagnostic exploratory laparoscopy to achieve complete cytoreduction in harmony with the patient's clinical and performance status, rather than focusing solely on tumor burden. The score showed high success rates for complete cytoreduction and also was useful in terms of predicting the morbidity and mortality. However, the Cukurova score study was conducted in single center. Validation of scores in centers with different capacities is expected to facilitate their widespread use and acceptance. Therefore, in this study, the investigators plan to conduct a validation study of the score in a total of 20 centers in Turkey, including our center. This study aims to evaluate the validity of the Cukurova score in predicting outcomes of primary cytoreduction in advanced ovarian cancer patients and thus determining the decision for primary cytoreductive surgery or neoadjuvant chemotherapy followed by interval cytoreductive surgery.

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
Cukurova Score Validation Study in Prediction of Primary Cytoreduction in Advanced Ovarian Cancer
Plain-language title
Checks a score for choosing surgery first in advanced ovarian cancerGenerated from the registry record. The registry title is the official one.
AI summary
From the trial's eligibility criteria. Read by machine on 12 November 2026.
Fit questions
Built from NCT06378905, who can take part
Record updated
29 August 2024