Cervical Dysplasia Clinical Trial
— LLETZ-MCOfficial title:
Performance of Large Loop Excision of the Transformation Zone (LLETZ) in Women With Cervical Dysplasia in the Follicular Phase Versus the Luteal Phase of the Menstrual Cycle: a Prospective Randomized Trial
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 preventive smear test at the gynecologist 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 dysplastic lesions are then surgically removed if necessary (conization). There are few data in the literature on the influence of the menstrual cycle on the bleeding pattern during and after conization. Hormonal variations during the menstrual cycle affect both the extent of blood flow to reproductive organs and hemostasis. In the follicular phase, there is a decrease in local blood flow in the uterus and pelvic organs and an increase in coagulability. Conversely, in the luteal phase there is an increase in local blood supply and a decrease in coagulability. Therefore, it seems reasonable to perform conization in the follicular phase to possibly reduce the extent and incidence of bleeding and bleeding complications. This assumption is supported by clinical observations. For example, there is evidence from other specialties that selection of the timing of surgery, taking into account the menstrual phase, may influence the risk of bleeding. Another factor of interest in menstruation-based surgical planning is psychological vulnerability, which may also vary with the menstrual cycle. Until now, consideration of the menstrual cycle in surgical planning for conization has not been standard practice and there is no recommendation in this regard in the current S3 guideline of the German Society of Gynecology and Obstetrics. Therefore, this study now aims to answer the question under prospective randomized conditions whether LLETZ conization performed during the follicular phase results in lower blood loss and higher patient satisfaction and lower anxiety scores compared to LLETZ conization performed during the luteal phase.
Status | Not yet recruiting |
Enrollment | 152 |
Est. completion date | December 2025 |
Est. primary completion date | October 2025 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Written consent - Regular menstrual cycle, defined as an interval between 21 and 35 days and a bleeding duration between 3 and 10 days during the last 3 months - Colposcopy performed preoperatively - Histologically (by previously performed colposcopy) confirmed dysplasia (CIN 1, CIN 2 or CIN 3) - Suspicion of low-grade or high-grade squamous intraepithelial lesion based on Papanicolaou smear with inconclusive colposcopy and need for surgical workup to exclude lesions - Age >18 years Exclusion Criteria: - Pregnant patients - Patients with insufficient knowledge of the German language - Pre-existing oncological diseases - Blood coagulation disorders - Taking blood thinning substances - Use of a hormonal intrauterine device (e.g. Mirena); - Use of a progesterone pill or progesterone injectate; - Use of long cycle contraceptive (no monthly bleeding). |
Country | Name | City | State |
---|---|---|---|
Germany | Marien Hospital Herne | Herne | North Rhine-Westphalia |
Lead Sponsor | Collaborator |
---|---|
Ruhr University of Bochum |
Germany,
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* Note: There are 17 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Intraoperative blood loss (weight) | The intraoperative blood loss, measured by the net-weight (in grams) of the surgical swabs used for hemostasis | During surgery | |
Secondary | Intraoperative blood loss (Hb) | The intraoperative blood loss, assessed through the difference between the Hb values measured preoperatively and 2 hours postoperatively, respectively. | Day of surgery | |
Secondary | Intraoperative blood loss (subjective) | The extent of intraoperative blood loss estimated by the surgeon (blinded to menstrual cycle phase) using a subjective categorization (mild, moderate, severe). | Immediately after surgery | |
Secondary | Postoperative bleeding (subjective) | The extent of postoperative bleeding during the first 24 hours after surgery (assessed by the patient using an 11-item Numerical Rating Scale; 0 [minimal bleeding] - 10 [strong bleeding]). | Interview 14 days after surgery | |
Secondary | Postoperative bleeding (days) | The number of postoperative days where bleeding occurred | Interview 14 days after surgery | |
Secondary | Patient's anxiety | The patient's anxiety level due to surgery as measured by the Spielberger State-Trait Anxiety Inventory (STAI, situational anxiety STAI-S, trait anxiety, STAI-T). Score range 20 to 80 points for each of the two parts of the test (a higher score means higher levels of anxiety). | On the day of surgery, before surgery | |
Secondary | Rate of complications | The occurring intra- and postoperative complications in a period within 14 days after surgery | During surgery up to 14 days post surgery | |
Secondary | Cone mass | The weight of the cone specimen (measured in grams in the unfixed state) | During surgery, immediately after the excision | |
Secondary | Procedure duration | Duration of the procedure (from start until complete hemostasis is achieved) | At surgery | |
Secondary | Patient satisfaction | Overall patient satisfaction (11-item numerical rating scale). | At discharge and 14 days after surgery |
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