Actively Recruiting

Phase Not Applicable
Age: 35Years - 50Years
FEMALE
NCT05856838

NovaSure Study: Endometrial Ablation in Women With Heavy Menstrual Bleeding

Led by University Hospital, Ghent · Updated on 2025-12-26

30

Participants Needed

1

Research Sites

161 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Heavy menstrual bleeding (HMB) affects 30% of women worldwide. It negatively influences physical activity, work productivity, sexual life and overall quality of life. In 2018, the FIGO (International Federation of Gynaecology and Obstetrics) revised its definition of AUB (FIGO-AUB system 1) and the classification of the underlying causes (FIGO-AUB system 2). It includes HMB, which is a subjective parameter and therefore patient determined. The FIGO-AUB system 2 describes the underlying causes of AUB through the acronym PALM-COEIN: Polyps, Adenomyosis, Leiomyomatosis, Malignancy, Coagulopathy, Endometrial, Iatrogenic and not otherwise specified. The National Institute for Health and Care Excellence (NICE) guideline on HMB recommends the levonorgestrel-releasing intrauterine system (LNG-IUS) 52 mg as the treatment of first choice in women with no identified pathology, fibroids less than 3cm in diameter, which are not causing distortion of the uterine cavity, or adenomyosis. If a woman declines a LNG-IUS, non-hormonal (fibrinolytics or non-steroidal anti-inflammatory drugs (NSAIDs)) and other hormonal pharmacological treatments can be considered. If treatment is unsuccessful, the woman declines pharmacological treatment, or symptoms are severe, an endometrial ablation (EA) or hysterectomy can be an alternative option. The latter is a definitive solution, but it is an invasive option, with a risk of serious complications. An EA is a procedure that destroys the endometrium. It aims to reduce the menstrual flow, sometimes causing amenorrhea. Initially, it was performed through hysteroscopy. Later on, second-generation devices became available. NovaSure is an example of a second-generation EA device, using a bipolar radiofrequency impedance-controlled system that evaporates endometrial tissue. The EA procedure is a minimally invasive alternative to hysterectomy. It is known to result in amenorrhea in 50% of women, with satisfaction rates between 80-96% and reported reintervention rates around 10%. Moreover, it is feasible to perform the procedure using only local anaesthesia. The investigators aim to assess the patient acceptability and feasibility of NovaSure EA in an outpatient setting with a short observation (≤4 hours) This observational prospective cohort study will be performed in the Ghent University Hospital (Ghent), Leuven Catholic University Hospital (Leuven) and Turnhout General Hospital (Turnhout). The surgeon performing the procedure will be the same per institution. The duration of the study is estimated at 4 months.

CONDITIONS

Official Title

NovaSure Study: Endometrial Ablation in Women With Heavy Menstrual Bleeding

Who Can Participate

Age: 35Years - 50Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 35 and 50 years
  • Heavy menstrual bleeding with PBAC score of 150 or higher
  • Unsuccessful drug treatment, contraindication to drug treatment, or patient declined drug treatment
  • No intra-uterine abnormalities on diagnostic hysteroscopy
  • Normal endometrial biopsy (pipelle)
  • Completed childbearing
Not Eligible

You will not qualify if you...

  • Pregnancy
  • Endometritis
  • Adenomyosis
  • Contraindication for local anaesthetics
  • Severe systemic disease (ASA 3 or higher)
  • Previous endometrial ablation
  • Poor understanding of Dutch language
  • History of pelvic malignancy
  • Presence of an intrauterine device (IUD)
  • Uterine cavity pathology (myoma or septum)
  • Uterine cavity length less than 4 cm
  • Any uterine incision other than a conventional cesarean incision

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Ghent University Hospital

Ghent, East Flanders, Belgium, 9000

Actively Recruiting

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Research Team

S

Studies Vrouwenkliniek

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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