Large Loop Excision of the Transformation Zone During Follicular Vs. Luteal Phase of the Menstrual Cycle (LLETZ-MC)

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18+
SponsorRuhr University of Bochum

About this 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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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)

Disqualifiers

Pregnant patients

Patients with insufficient knowledge of the German language

Pre-existing oncological diseases

Blood coagulation disorders

Trial design

Design model

Parallel

Treatments tested in this trial

  • LLETZ

    Procedure/Surgery

    Large loop excision of the transformation zone

Treatment groups

152 Participants
are divided into 2 treatment groups
Group A: Follicular phaseOther 1 intervention
Group B: Luteal phaseOther 1 intervention

Trial outcomes

Primary outcomes

1

Intraoperative blood loss (weight)

The intraoperative blood loss, measured by the net-weight (in grams) of the surgical swabs used for hemostasis

Time frame
During surgery

Secondary outcomes

1

Intraoperative blood loss (Hb)

The intraoperative blood loss, assessed through the difference between the Hb values measured preoperatively and 2 hours postoperatively, respectively.

Time frame
Day of surgery
2

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).

Time frame
Immediately after surgery
3

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 \[strong bleeding\]).

Time frame
Interview 14 days after surgery
4

Postoperative bleeding (days)

The number of postoperative days where bleeding occurred

Time frame
Interview 14 days after surgery

Other outcomes

Sponsors and contacts

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