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The Use of a Morcellator in Operative Hysteroscopy for Benign Intracavitary Lesions: a Feasibility Study

Primary Purpose

Endometrial Polyp Benign, Retained Products of Conception, Myoma;Uterus

Status
Completed
Phase
Not Applicable
Locations
Belgium
Study Type
Interventional
Intervention
Hysteroscopic morcellation 19 Fr. intrauterine BIGATTI Shaver for uterine intracavitary lesions
Sponsored by
Universitaire Ziekenhuizen KU Leuven
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Endometrial Polyp Benign focused on measuring Endometrial polyp, Hysteroscopic surgery, Morcellation, Retained products of conception, Myoma

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria: Patients: Female Ultrasonographic diagnosis of an intracavitary lesion, according the IETA terms and definitions endometrial polyp FIGO 0-1 myoma (maximum diameter 2 cm) RPOC (maximum diameter 2 cm, no enhanced myometrial vascularity) Exclusion Criteria: • Active vaginal bleeding (possible) malignancy < 18y Patient refusal Pregnancy Impossibility to access the uterine cavity (e.g. severe cervical stenosis) Absence of intracavitary lesion (endometrial polyp, FIGO 0-1 myoma or RPOC) at hysteroscopy

Sites / Locations

  • Ziekenhuis Oost-Limburg
  • University Hospitals Leuven

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Hysteroscopic morcellation 19 Fr. intrauterine BIGATTI Shaver for uterine intracavitary lesions

Arm Description

Single experimental arm of patients with a intracavitary lesion and elligible for hysteroscopic morcellation.

Outcomes

Primary Outcome Measures

Completeness of resection of intracavitary lesions in 50 patients, when using a hysteroscopic Bigatti Shaver.
If all tissue could be removed by the 19 Fr. intrauterine BIGATTI Shaver by direct visualisation at the end of the hysteroscopic procedure and at post-operative ultrasound evaluation.

Secondary Outcome Measures

Operation time
total operation time and time necessary for the morcellation
Need for cervical dilation during procedure
Was it necessary to perform any dilatation with
Volume of distension fluid used / loss (deficit) during procedure
Deficit in fluid used during surgery?
Operator satisfaction, assessed by verbal rating scale
Operator satisfaction in terms of technique, ergonomics and general proceedings. The verbal rating scale includes Very negative; Negative; Intermediate; Positive; Very positive.
Complications
Adverse events during procedure/hospitalization and within the first 6 weeks after procedure
Pain on the first postoperative day, assessed by verbal rating scale
Pain on the first day post-operatively. The verbal rating scale includes Very negative; Negative; Intermediate; Positive; Very positive.
Histology of the intracavitary lesion
Incidence of histological outcomes such as endometrial polyps, intracavitary myomas or remnant products of conception. This is a categorical variable.

Full Information

First Posted
February 7, 2023
Last Updated
July 13, 2023
Sponsor
Universitaire Ziekenhuizen KU Leuven
Collaborators
Ziekenhuis Oost-Limburg
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1. Study Identification

Unique Protocol Identification Number
NCT05811286
Brief Title
The Use of a Morcellator in Operative Hysteroscopy for Benign Intracavitary Lesions: a Feasibility Study
Official Title
The Use of a Morcellator in Operative Hysteroscopy for Benign Intracavitary Lesions: a Feasibility Study
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
May 20, 2021 (Actual)
Primary Completion Date
June 28, 2023 (Actual)
Study Completion Date
June 28, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Universitaire Ziekenhuizen KU Leuven
Collaborators
Ziekenhuis Oost-Limburg

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Polyps, intracavitary myomas and retained products of conception (RPOC) are common benign intracavitary lesions of the uterus and frequently cause abnormal uterine bleeding or pain. In general, intracavitary lesions are treated by operative hysteroscopy with bipolar resectoscopic removal under general anaesthesia, performed in the theatre (OR). Potential problems with this approach are thermal damage and impairment of visibility due to loose tissue fragments necessitating multiple entries for tissue removal. Recently, lesion morcellation by hysteroscopy has been introduced as an alternative technique. Compared to the resectoscopic approach, morcellation is reportedly associated with a shorter total procedure time, smaller fluid deficit and number of insertions. A few trials also registered a higher success rate in completeness of resection. No significant differences in odds of surgical complications have been reported. Most hysteroscopic morcellators have diameters up to 8 mm, for which cervical dilation under general anaesthesia is usually needed. Recently, companies have developed hysteroscopic morcellators with smaller diameters, e.g. 6.3 mm for the 19 Fr. intrauterine BIGATTI Shaver (IBS®). This means less need for cervical dilation, and potential use without anesthesia. At this moment, there are no prospective studies available on feasibility of the 19 Fr. intrauterine BIGATTI Shaver (IBS®). Before implementing hysteroscopic morcellation in our department, we need a feasibility study assessing the method in standard conditions in the operation room or in ambulatory setting under sedation. Trial objectives: Assessment of the feasibility of hysteroscopic morcellation of benign uterine intracavitary lesions. The primary objective is to assess the completeness of hysteroscopic resection in patients undergoing the procedure under general anesthesia or sedation. Secondary objectives are to assess perioperative parameters as operation time, need for cervical dilation, adverse events, pain, operator satisfaction; to assess quality of tissue for histological examination; to assess postoperative complications and pain.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Endometrial Polyp Benign, Retained Products of Conception, Myoma;Uterus
Keywords
Endometrial polyp, Hysteroscopic surgery, Morcellation, Retained products of conception, Myoma

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
56 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Hysteroscopic morcellation 19 Fr. intrauterine BIGATTI Shaver for uterine intracavitary lesions
Arm Type
Experimental
Arm Description
Single experimental arm of patients with a intracavitary lesion and elligible for hysteroscopic morcellation.
Intervention Type
Procedure
Intervention Name(s)
Hysteroscopic morcellation 19 Fr. intrauterine BIGATTI Shaver for uterine intracavitary lesions
Intervention Description
With the shaver, the lesion is removed in the OR. We will include endometrial polyps, FIGO 0-1 myomas and retained products of conception. We will assess the completeness of hysteroscopic resection, operation time, need for cervical dilation, adverse events, pain, operator satisfaction; quality of tissue for histological examination, postoperative complications and pain.
Primary Outcome Measure Information:
Title
Completeness of resection of intracavitary lesions in 50 patients, when using a hysteroscopic Bigatti Shaver.
Description
If all tissue could be removed by the 19 Fr. intrauterine BIGATTI Shaver by direct visualisation at the end of the hysteroscopic procedure and at post-operative ultrasound evaluation.
Time Frame
During surgery
Secondary Outcome Measure Information:
Title
Operation time
Description
total operation time and time necessary for the morcellation
Time Frame
During surgery
Title
Need for cervical dilation during procedure
Description
Was it necessary to perform any dilatation with
Time Frame
During surgery
Title
Volume of distension fluid used / loss (deficit) during procedure
Description
Deficit in fluid used during surgery?
Time Frame
During surgery
Title
Operator satisfaction, assessed by verbal rating scale
Description
Operator satisfaction in terms of technique, ergonomics and general proceedings. The verbal rating scale includes Very negative; Negative; Intermediate; Positive; Very positive.
Time Frame
At the end of the procedure
Title
Complications
Description
Adverse events during procedure/hospitalization and within the first 6 weeks after procedure
Time Frame
6 weeks after surgery
Title
Pain on the first postoperative day, assessed by verbal rating scale
Description
Pain on the first day post-operatively. The verbal rating scale includes Very negative; Negative; Intermediate; Positive; Very positive.
Time Frame
Day 1 post-operatively
Title
Histology of the intracavitary lesion
Description
Incidence of histological outcomes such as endometrial polyps, intracavitary myomas or remnant products of conception. This is a categorical variable.
Time Frame
6 weeks post-operatively

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients: Female Ultrasonographic diagnosis of an intracavitary lesion, according the IETA terms and definitions endometrial polyp FIGO 0-1 myoma (maximum diameter 2 cm) RPOC (maximum diameter 2 cm, no enhanced myometrial vascularity) Exclusion Criteria: • Active vaginal bleeding (possible) malignancy < 18y Patient refusal Pregnancy Impossibility to access the uterine cavity (e.g. severe cervical stenosis) Absence of intracavitary lesion (endometrial polyp, FIGO 0-1 myoma or RPOC) at hysteroscopy
Facility Information:
Facility Name
Ziekenhuis Oost-Limburg
City
Genk
Country
Belgium
Facility Name
University Hospitals Leuven
City
Leuven
ZIP/Postal Code
3000
Country
Belgium

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
We will share general descriptive characteristics of our cohort. This includes patient and operative characteristics, final histology and patient and doctor reported outcomes.
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The Use of a Morcellator in Operative Hysteroscopy for Benign Intracavitary Lesions: a Feasibility Study

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