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Treatment of Missed Miscarriage With TRUCLEAR Tissue Removal System, a Feasiblity Study

Primary Purpose

Miscarriage

Status
Completed
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
TRUCLEAR tissue removal system
Sponsored by
Assuta Ashdod Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Miscarriage

Eligibility Criteria

21 Years - 45 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Patients with missed miscarriage up to 10 weeks from the last menstrual period
  • Patients are able to provide written consent
  • Patients with no underlying medical conditions

Exclusion Criteria:

  • Inability to consent due to cognitive or language barrier
  • Any underlying medical condition requiring medical treatment
  • Documented failed hysteroscopy prior to the current referral
  • Inability to consent due to cognitive or language barrier
  • Uterine malformations or fibroids
  • Previous cesarean section

Sites / Locations

  • Assuta Ashdod University Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

TRUCLEAR TREATMENT

Arm Description

patients up to 10 weeks of gestation with missed miscarriage undergoing evacuation of products of conception using the TRUCLEAR tissue removal system under direct hysteroscopic visualization

Outcomes

Primary Outcome Measures

Number of cases with retained products of conception following the procedure
Number of cases in which the procedure could not be completed using under vision hysteroscopic morcellation

Secondary Outcome Measures

number of complications according to Dindo-Clavien scale
number of any complications according to the Dindo-Clavien scale, especially uterine perforation, infection, bleeding and pain that requires admission
incomplete removal
number of patients with retained products of conception on ultrasound scan or hysteroscopy

Full Information

First Posted
August 11, 2020
Last Updated
August 20, 2023
Sponsor
Assuta Ashdod Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04512820
Brief Title
Treatment of Missed Miscarriage With TRUCLEAR Tissue Removal System, a Feasiblity Study
Official Title
Embryoscopic Evacuation of Early Missed Abortion Using the TRUCLEAR Hysteroscopic Morcellator System a Feasibility Study
Study Type
Interventional

2. Study Status

Record Verification Date
January 2020
Overall Recruitment Status
Completed
Study Start Date
March 5, 2020 (Actual)
Primary Completion Date
January 12, 2021 (Actual)
Study Completion Date
January 12, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assuta Ashdod Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
the Aim of this study is to prospectively study the feasibility of evacuation of products of conception (POC) in missed miscarriages up to 10 weeks using the TRUCLEAR tissue removal system in order to achieve targeted treatment under direct vision of the POC and thus potentially reducing the risk of complications and intrauterine adhesions
Detailed Description
Embryoscopy and fetoscopy had been used increasingly in the treatment of missed abortions in the last two decades. This is done simply by transcervical hysteroscopy during pregnancy. The fact that we can directly view the embryo in the gestational sack allows us to document and describe the fetal morphology and to note different anatomical malformations. Phillips et al. described in 2001 the use of embryoscopy prior to evacuation of the uterus in early missed abortions in order to diagnose anatomical malformations and to allow sampling of the fetal tissues for genetic testing. This group also demonstrated that patients with repeated pregnancy loss are more likely to have morphologically normal embryos and less aneuploidy in cytogenetic analysis. The use of fetal tissue obtained in embryoscopy allows for more accurate genetic testing and diagnosis and reduces the number of maternal cells in the specimen. Hysteroscopic morcellation had been used for intrauterine tissue extraction for over 20 years. Hysteroscopic morcellators have been shown to allow for rapid and complete resection of polyps, fibroids, uterine septa, and retained products of conception. These instruments use a rotating blade and a suction system that allows for the removal of the specimen under direct hysteroscopic visualization. When compared with standard resectoscopic technique, the use of hysteroscopic morcellators probably saves time and allows for more complete removal of the specimen. Use of the hysteroscopic morcellator for resection of the fetal tissue in early missed abortions might prove beneficial over the standard blind Dilatation and curettage currently used to treat this condition. This technique might allow selective targeting of the fetal tissue thus decreasing the damage caused by trauma to the entire uterine cavity. In a recent systematic review the rate of intrauterine adhesions following D&C for missed abortions ranged between 16 to 21 percent. This technique was assessed in one case for a woman with previous Ashreman's syndrome and was found to be feasible although the authors state that visibility was poor while resecting the implantation site due to high vascularization. The primary aim of the current study is to assess the feasibility of embryolysis - resection of an early missed abortion with the Truclear 8 mm hysteroscopic morcellator. Secondary aims include the rate of complications, incomplete removal and intrauterine adhesions. In this pilot feasibility study, we hypothesize that the 8mm Truclear Morcellator system will be able to achieve full evacuation of the uterine cavity. Performed under direct visualization and focused only on the implantation site, thus reducing the potential for further intrauterine adhesions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Miscarriage

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
TRUCLEAR TREATMENT
Arm Type
Experimental
Arm Description
patients up to 10 weeks of gestation with missed miscarriage undergoing evacuation of products of conception using the TRUCLEAR tissue removal system under direct hysteroscopic visualization
Intervention Type
Device
Intervention Name(s)
TRUCLEAR tissue removal system
Other Intervention Name(s)
non
Intervention Description
evacuation of POC using the TRUCLEAR tissue removal system
Primary Outcome Measure Information:
Title
Number of cases with retained products of conception following the procedure
Description
Number of cases in which the procedure could not be completed using under vision hysteroscopic morcellation
Time Frame
immediate - during the procedure
Secondary Outcome Measure Information:
Title
number of complications according to Dindo-Clavien scale
Description
number of any complications according to the Dindo-Clavien scale, especially uterine perforation, infection, bleeding and pain that requires admission
Time Frame
within six weeks from the procedure
Title
incomplete removal
Description
number of patients with retained products of conception on ultrasound scan or hysteroscopy
Time Frame
within 8 weeks

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Patients with missed miscarriage up to 10 weeks from the last menstrual period Patients are able to provide written consent Patients with no underlying medical conditions Exclusion Criteria: Inability to consent due to cognitive or language barrier Any underlying medical condition requiring medical treatment Documented failed hysteroscopy prior to the current referral Inability to consent due to cognitive or language barrier Uterine malformations or fibroids Previous cesarean section
Facility Information:
Facility Name
Assuta Ashdod University Hospital
City
Ashdod
Country
Israel

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
only unidentified data will be shared
Citations:
PubMed Identifier
11464580
Citation
Philipp T, Kalousek DK. Transcervical embryoscopy in missed abortion. J Assist Reprod Genet. 2001 May;18(5):285-90. doi: 10.1023/a:1016666301481.
Results Reference
background
PubMed Identifier
27743696
Citation
Feichtinger M, Wallner E, Hartmann B, Reiner A, Philipp T. Transcervical embryoscopic and cytogenetic findings reveal distinctive differences in primary and secondary recurrent pregnancy loss. Fertil Steril. 2017 Jan;107(1):144-149. doi: 10.1016/j.fertnstert.2016.09.037. Epub 2016 Oct 12.
Results Reference
background
PubMed Identifier
25779005
Citation
Campos-Galindo I, Garcia-Herrero S, Martinez-Conejero JA, Ferro J, Simon C, Rubio C. Molecular analysis of products of conception obtained by hysteroembryoscopy from infertile couples. J Assist Reprod Genet. 2015 May;32(5):839-48. doi: 10.1007/s10815-015-0460-z. Epub 2015 Mar 17.
Results Reference
background
PubMed Identifier
27164165
Citation
Shazly SA, Laughlin-Tommaso SK, Breitkopf DM, Hopkins MR, Burnett TL, Green IC, Farrell AM, Murad MH, Famuyide AO. Hysteroscopic Morcellation Versus Resection for the Treatment of Uterine Cavitary Lesions: A Systematic Review and Meta-analysis. J Minim Invasive Gynecol. 2016 Sep-Oct;23(6):867-77. doi: 10.1016/j.jmig.2016.04.013. Epub 2016 May 7.
Results Reference
background
PubMed Identifier
27436757
Citation
Hooker A, Fraenk D, Brolmann H, Huirne J. Prevalence of intrauterine adhesions after termination of pregnancy: a systematic review. Eur J Contracept Reprod Health Care. 2016 Aug;21(4):329-35. doi: 10.1080/13625187.2016.1199795.
Results Reference
background
PubMed Identifier
24865632
Citation
Harpham M, Abbott J. Use of a hysteroscopic morcellator to resect miscarriage in a woman with recurrent Asherman's syndrome. J Minim Invasive Gynecol. 2014 Nov-Dec;21(6):1118-20. doi: 10.1016/j.jmig.2014.05.006. Epub 2014 May 24.
Results Reference
background
PubMed Identifier
33951488
Citation
Weinberg S, Pansky M, Burshtein I, Beller U, Goldstein H, Barel O. A Pilot Study of Guided Conservative Hysteroscopic Evacuation of Early Miscarriage. J Minim Invasive Gynecol. 2021 Nov;28(11):1860-1867. doi: 10.1016/j.jmig.2021.04.017. Epub 2021 May 2.
Results Reference
derived

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Treatment of Missed Miscarriage With TRUCLEAR Tissue Removal System, a Feasiblity Study

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