Comparison of the Effects of Vaginal Cuff Closure Sexual Function in Laparoscopic Hysterectomy

November 13, 2025 updated by: merve ecem albayrak, Acibadem Kent Hospital

Comparison of the Effects of Vaginal Cuff Closure Techniques on Vaginal Length and Sexual Function in Laparoscopic Hysterectomy

Aim: Laparoscopic hysterectomy is the vaginal removal of the uterus with the help of laparoscopy. After the uterus is removed after hysterectomy, vaginal length is shortened by cuff suturing, resulting in conditions such as dyspareunia and sexual dysfunction . Hysterectomy may also affect women physically and psychologically, as well as causing changes in sexual functions . In patients planned to undergo hysterectomy; Changes that may occur in sexual functions cause serious concerns during the preoperative period. However, physicians often miss these important points and do not discuss these issues adequately with patients. In this study; We aimed to compare the effects of vaginal cuff closure techniques in laparoscopic hysterectomy on vaginal length and women's sexual life. We used the Arizona Sexual Experience Scale to assess women's sexual life.

Study Overview

Detailed Description

Hysterectomy, defined as the surgical removal of the uterus, is one of the most commonly performed gynecological operations worldwide. Indications for hysterectomy, which is frequently performed on women of reproductive age and menopause, are emphasized in the literature as including pelvic masses (uterine myomas), abnormal bleeding (menorrhagia, menometrorrhagia, dysfunctional uterine bleeding), ovarian cysts, endometriosis, pelvic pain, pelvic prolapse, and urinary incontinence. Currently, there are many approaches to hysterectomy. The uterus can be removed abdominally, vaginally, laparoscopically, or robotically. Due to the advantages of minimally invasive surgery, laparoscopic and robotic hysterectomies are on the rise, while the rate of vaginal and abdominal hysterectomies is decreasing. Laparoscopic hysterectomy is the vaginal removal of the uterus using laparoscopy. Advantages include rapid postoperative recovery, short hospital stay, reduced need for analgesia, and improved visualization of the pelvic organs. Hysterectomy can lead to bleeding, infection, thromboembolic events, and gastrointestinal and urinary complications. Due to the removal of the uterus after hysterectomy, vaginal length shortens, leading to conditions such as dyspareunia and sexual dysfunction. Hysterectomy can also affect women physically and psychologically, as well as alter sexual function. Sexual function after hysterectomy can be affected by physiological factors (reduced tissue quality, neural stimulation, and pelvic blood flow due to anatomical changes in pelvic tissue), hormonal factors (reduced ovarian blood flow or decreased estrogen and progesterone levels due to the removal of the ovaries along with hysterectomy), psychological factors (depression, altered body image, and perception of femininity), and factors related to the hysterectomy technique. There are conflicting opinions regarding the effect of the uterus on sexual function. Some authors suggest that uterine contractions play an important role in the orgasmic phase, while others suggest that hysterectomy causes vaginal shortening or damage to autonomic nerve endings in the cervicovaginal area, leading to sexual dysfunction. The causal relationship between hysterectomy and decreased sexual function has been linked to shortened vaginal length and the emergence of postoperative dyspareunia. This is influenced by the vaginal cuff closure techniques used during hysterectomy.

Research on the relationship between hysterectomy and postoperative urinary incontinence or urogenital complaints has yielded mixed results. Studies report varying effects of hysterectomy on urinary incontinence. However, it is unclear whether postoperative urinary incontinence is due to the hysterectomy itself, influenced by the technique, or due to preoperative factors. The possibility of deterioration in sexual function and urinary dysfunction in patients undergoing hysterectomy raises serious concerns during the preoperative period. However, physicians often overlook these important points and fail to adequately discuss them with patients. In this study, we aimed to investigate the effects of the vaginal cuff closure technique in laparoscopic hysterectomy on women's sexual life and urogenital functions. We used the Arizona Sexual Experiences Scale and vaginal length measurement to assess women's sexual life, and the Urogenital Distress Inventory to assess urogenital functions. Patients who underwent laparoscopic hysterectomy at the Obstetrics and Gynecology Department of Abant İzzet Baysal University Faculty of Medicine will be included in this study. Patients who underwent total laparoscopic hysterectomy will be divided into two groups based on the vaginal cuff closure technique: laparoscopic and vaginal. Patients will be recorded and evaluated based on their age, gender, parity, body mass index, presenting complaints, ultrasonography findings, probe curettage results, Pap smear results, surgical indications, current chronic diseases, and past surgical history. Data obtained in the study will be analyzed using SPSS. During total laparoscopic hysterectomy, vaginal cuff closure techniques will be used to divide the patients into two groups: laparoscopic and vaginal closure.

Study Type

Expanded Access

Expanded Access Type

  • Intermediate-size Population

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Perimenopausal period
  • Having undergone surgery for benign gynecological indications
  • Complete and accurate patient registration information.
  • Volunteering to participate in the study.

Exclusion Criteria:

  • Uterus size greater than 14 weeks' gestation
  • Pelvic organ prolapse in the preoperative period
  • Urinary incontinence in the preoperative period
  • Cases with intraoperative complications
  • Having undergone another concurrent surgery (urinary incontinence surgery, bowel surgery, etc.)
  • History of endometriosis
  • History of pelvic inflammatory disease

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Collaborators and Investigators

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Publications and helpful links

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Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

First Submitted

November 10, 2025

First Submitted That Met QC Criteria

November 13, 2025

First Posted (Estimated)

November 14, 2025

Study Record Updates

Last Update Posted (Estimated)

November 14, 2025

Last Update Submitted That Met QC Criteria

November 13, 2025

Last Verified

November 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • AcibademKentH

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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