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NCT Number: NCT06977334

IOTA Ultrasound Criteria and Serum CA 125 for Ovarian Malignancy Detection

This cross-sectional analytic study assessed the diagnostic accuracy of IOTA Simple Rules versus serum CA 125 in women with adnexal masses undergoing surgery. Eighty-two percent of tumors were classifiable by IOTA criteria; CA 125 cut-offs of 35, 70, and 105 U/mL were evaluated against histopathology gold standard.

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Key information

About this study

All women admitted to the Department of Obstetrics and Gynecology and assigned for the surgery of adnexal mass were enrolled in the study. After written informed consent, the clinical proforma was filled up. Data collection regarding age, current or previous hormonal contraception, menopausal status and family history of breast or ovarian cancer, clinical presentation. Participants were scheduled for ultrasound evaluation done according to IOTA simple rules (five malignant features and five benign features) and peripheral blood was collected for tumor marker serum CA125 measurement.

During ultrasonographic examination, the morphology of the adnexal masses was characterized using 2D real-time and color Doppler ultrasound. Adnexal masses were described according to origin (ovarian/extra ovarian); position (right/left/bilateral); number of lesions; type of lesions (unilocular/unilocular - solid/multilocular/multilocular - solid); size; volume; intracystic fluid echogenicity; number of locations; presence and size of septations; presence, number, size of solid papillary projections; largest solid component; presence / absent of ascites. These parameters are used as designation according to IOTA Group.

For the sample of CA125, approximately 2 ml blood was collected and registered patient's hospital number, then the selected reagent was added to the sample and kept in a fully automated immunoassay system in the hospital laboratory where electrochemiluminescence Immunoassay method (ECLIA) is used for the analysis. Surgery was performed in the hospital and a biopsy was sent for the histopathology examination in the same hospital.

Sensitivity, specificity, positive predictive value, and negative predictive values of CA125 and IOTA class were calculated. The correlation between CA 125 and IOTA simple rules was analyzed and compared with histopathological reports using the Pearson correlation method. The area under the receiver operating characteristic curve (AUC) was used to determine the point at which CA125 had the highest sensitivity and specificity in distinguishing histologically malignant from benign tumors.

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • All age groups and parity with ovarian mass admitted for scheduled surgery.

Exclusion criteria

  • Proven cases of ovarian malignancy
  • Ovarian mass in pregnancy

Treatment and study plan

Primary outcomes

  1. Sensitivity of IOTA Simple Rules

    Time frame: At surgery/histopathology

    Proportion of histologically malignant masses correctly identified by IOTA criteria.

  2. Specificity of IOTA Simple Rules

    Time frame: At surgery/histopathology

    Proportion of histologically malignant masses correctly identified by IOTA criteria.

  3. Sensitivity of Serum CA 125 (cut-off 35 U/mL)

    Time frame: Preoperative blood draw

    Proportion of malignant tumors with CA 125 >35 U/mL.

  4. Specificity of Serum CA 125 (cut-off 35 U/mL)

    Time frame: Preoperative blood draw

    Proportion of benign tumors with CA 125 ≤35 U/mL.

  5. Area Under the ROC Curve for CA 125

    Time frame: Preoperative blood draw vs histopathology

    Discriminatory performance of CA 125 at multiple cut-off points.

Sponsors and collaborators

Lead sponsor

Maharajgunj Medical Campus

Other

Registry information

Official study title

Identification of Ovarian Malignancy With Ultrasonography Based Criteria (IOTA) and Serum CA 125

Acronym: IOTA-CA125

Important dates

Study start
2022
Primary completion
2022
Study completion
2022
First posted
May 18, 2025
Registry last updated
May 18, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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