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临床试验/NCT06802198
NCT06802198尚未招募不适用

Comparison of Long-Term Outcomes Following Laparoscopic Total Vs Supracervical Hysterectomy, a Randomized Clinical Trial

Fondazione Policlinico Universitario Agostino Gemelli IRCCS1 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2025年10月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
500
试验地点
1
主要终点
Quality of life and patient's impression of improvement at 36 months after surgery

研究概览

简要总结

The goal of this randomized clinical trial is to assess the outcomes of total laparoscopic hysterectomy vs subtotal laparoscopic hysterectomy + mini-laparotomy for uterine extraction for benign gynecological conditions in terms of change in quality of life at 36 months after surgery and patient's impression of improvement. The secondary objectives of the study are to assess any differences in terms of peri and postoperative outcomes (postoperative pain, blood loss, hospital stay, intraoperative or short and long-term postoperative complications, long term urinary, bowel and pelvic floor symptoms, prevalence of vaginal cuff dehiscence).

Participants will fill the following questionnaires pre-operatively and at the follow up:

  • Short Form 36 (SF36),
  • Euro Quality of life 5D-3L (EQ 5D-3L)
  • Female Sexual Function Index (FSFI)
  • Patient Global Impression of Improvement (PGI-I) only during the follow-up period.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •Age>18 years
  • •Signed informed consent

排除标准

  • •Uterine or adnexal pathology suspect for malignancy
  • •Abnormal or unknown PAP test
  • •Patients with invasive neoplasia in the previous 5 years (excluding non-melanoma skin tumors, breast cancer T1 N0 M0 Grade 1 or 2 without signs of recurrence or activity).
  • •Previous radical pelvic surgery or radiotherapy;
  • •Age > 80 years
  • •Pregnant patients
  • •Desire for further pregnancies
  • •Contraindications to general anaesthesia or to the Trendelenburg position
  • •Refusal to sign informed consent

研究组 & 干预措施

patients undergoing total hysterectomy

Active Comparator

Total hysterectomy involves the complete removal of the uterus including the cervix

干预措施: total hysterectomy (Procedure)

patients undergoing subtotal hysterectomy

Experimental

Subtotal hysterectomy involves the removal of the upper part of the uterus preserving the cervix

干预措施: subtotal hysterectomy (Procedure)

结局指标

主要结局

Quality of life and patient's impression of improvement at 36 months after surgery

时间窗: 5 years

To assess the impact of surgery on patients' quality of life measured by the Physical Functioning items of SF36 questionnaire, at 36 months after surgery

次要结局

  • Postoperative pain(5 years)
  • Intra-operative data(5 years)
  • intraoperative complications(5 years)
  • short and long-term postoperative complications(5 years)
  • Urinary, bowel and pelvic floor symptoms(5 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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