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NCT05378152Completed

Assessing the Benefit of Pipelle Biopsy in Patients With Postmenopausal Bleeding and an Atrophic-appearing Cavity

Is Pipelle Biopsy of Benefit in Patients With Postmenopausal Bleeding and an Atrophic-appearing Cavity?

Source: ClinicalTrials.gov · Last updated 23 Apr 2024

Brief summary (registry, in English)

Postmenopausal bleeding (PMB) is the occurrence of vaginal bleeding 12 months following a woman's last menstrual cycle. PMB represents one of the most common reasons for referral to gynaecology services. Approximately 10% of women with PMB will be found to have endometrial cancer. The gold standard of investigation of PMB is ambulatory gynaecology through the outpatient hysteroscopy clinic, which is often combined with Pipelle biopsy for endometrial sampling. Up to 60% of women that present with PMB will have an atrophic-appearing cavity at hysteroscopy. This provides a challenge in obtaining a histological sample through both dilatation \& curretage (D\&C) and Pipelle biopsy. Often, scant tissue that is insufficient for clinical diagnosis is obtained. Pipelle biopsy is associated with patient discomfort. It is also associated with costs related to the purchasing of equipment and the processing of samples in the laboratory to the sum of approximately 30 euro per sample. It is rare that a sample taken from an atrophic cavity will return any clinically meaningful result. A negative hysteroscopy reduces the probability of endometrial cancer to 0.6%. This study aims to compare patients with PMB and atrophic-appearing cavity that undergo pipelle biopsy to those that do not. Differences in pain scores, cost saving and differences in clinical follow up will be assessed to evaluate the benefit of Pipelle biopsy in patients with PMB and atrophic-appearing cavity.

Status (registry)
Completed
Study type
Interventional
Enrollment
82 (actual)
First submitted
3 May 2022
Start date
24 Sept 2022
Primary completion date
23 Feb 2024
Lead sponsor
Royal College of Surgeons, Ireland
NCT number
NCT05378152

What you commit to

  • Study type: Interventional
  • Participants enrolled: 82
  • From 24 Sept 2022 to the primary completion date, 23 Feb 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Obvious cause of bleeding from the vagina or cervix at time of hysteroscopy
  • History of endometrial hyperplasia/cancer

Other

  • Premenopausal
  • Any lesion requiring biopsy at time of hysteroscopy

Who the study is looking for

  • Postmenopausal
  • Postmenopausal bleeding
  • Tolerates hysteroscopy

Sex: Female · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Rotunda hospital
Coordinator of this site? Confirm its status
DublinIrelandUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.