RecruitingNot ApplicableNCT05132114

Large Loop Excision of the Transformation Zone (LLETZ) with Vs Without IntraOperative Application of Lugol's Iodine

Large Loop Excision of the Transformation Zone (LLETZ) with Versus Without Intraoperative Application of Lugol's Iodine in Women with Cervical Dysplasia: a Prospective Randomized Trial


Sponsor

Ruhr University of Bochum

Enrollment

216 participants

Start Date

Jan 17, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

Cervical cancer is one of the most common cancers in women and one of the leading causes of death in women worldwide. Pre-cancerous lesions (dysplasias) are detected by the gynecologist's preventive smear test and can thus contribute to a 100% chance of cure if they are clarified by a colposcopic examination as part of the dysplasia consultation and, if necessary, surgically removed. Conization (= surgical removal of a cone of tissue from the cervix) is the method of choice for removing the diseased tissue. LLETZ conization (Large Loop Excision of the Transformation Zone) is the worldwide standard surgical procedure for conization. There is risk of local persistence of the precancerous lesion if the cervical dysplasia is not completely removed. To minimize this, the iodine test can be used. Here, a 5% iodine solution (so-called Lugol's solution) is dabbed onto the cervix uteri, resulting in an intense and characteristic brown staining of the healthy cervical epithelium. Sites without staining are termed iodine negative and may contain dysplastic cells. The strength of iodine testing lies in its high specificity, i.e., the reliable ability to exclude false-positive results. The purpose of intraoperative iodine staining is to select the resection line with a high degree of certainty in healthy (i.e., iodine-positive) tissue in order to reduce the rate of cervical dysplasia that is not completely removed (so-called non-in-sano resection, or R1 resection). Systematic survey data from the dysplasia units certified in Germany on the question of the use of intraoperative iodine testing in Germany are lacking, as is the literature as a whole. For example, the current S3 guideline of the German Society of Gynecology and Obstetrics on the diagnosis and treatment of cervical dysplasia (as of March 2020) names intraoperative iodine testing only as a possible option for performing LLETZ. In this prospective, randomized study, the investigators aim to answer the question whether LLETZ performed with the help of an iodine test with selection of the resection line in the iodine-positive area leads to a lower rate of R1 resections compared to the standard LLETZ without iodine test.


Eligibility

Sex: FEMALEMin Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study compares two surgical approaches to removing abnormal cervical cells (dysplasia/pre-cancer) to see whether applying a special iodine solution during the procedure improves outcomes. **You may be eligible if...** - You are 18 or older - You have been diagnosed with cervical dysplasia (CIN 1, 2, or 3) confirmed by biopsy during colposcopy - You have had a colposcopy exam before surgery - You can provide written consent **You may NOT be eligible if...** - You are pregnant - You have an iodine allergy - You are taking blood-thinning medications or have a blood clotting disorder - You have already had a cervical procedure (such as prior cone biopsy) - You do not have adequate German language skills Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DIAGNOSTIC_TESTLugol's iodine test

Intraoperative application of Lugol's iodine (i.e. staining of the cervix with Lugol's iodine solution)


Locations(1)

Marien Hospital Herne

Herne, North Rhine-Westphalia, Germany

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NCT05132114


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