Treatment of Missed Miscarriage With TRUCLEAR Tissue Removal System, a Feasiblity Study
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT04512820 |
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Recruitment Status :
Recruiting
First Posted : August 14, 2020
Last Update Posted : August 14, 2020
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Miscarriage | Device: TRUCLEAR tissue removal system | Not Applicable |
Show detailed description
| Study Type : | Interventional (Clinical Trial) |
| Estimated Enrollment : | 10 participants |
| Allocation: | N/A |
| Intervention Model: | Single Group Assignment |
| Masking: | None (Open Label) |
| Primary Purpose: | Treatment |
| Official Title: | Embryoscopic Evacuation of Early Missed Abortion Using the TRUCLEAR Hysteroscopic Morcellator System a Feasibility Study |
| Actual Study Start Date : | March 5, 2020 |
| Estimated Primary Completion Date : | November 1, 2020 |
| Estimated Study Completion Date : | January 1, 2021 |
| Arm | Intervention/treatment |
|---|---|
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Experimental: TRUCLEAR TREATMENT
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
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Device: TRUCLEAR tissue removal system
evacuation of POC using the TRUCLEAR tissue removal system
Other Name: non |
- completion of the procedure [ Time Frame: immediate - during the procedure ]completion of the procedure undervision without need to resort to suction & curettage
- complications [ Time Frame: within two weeks from the procedure ]uterine perforation, infection, bleeding and pain that requires admission
- incomplete removal [ Time Frame: within 8 weeks ]presence of retained products of conception on ultrasound scan or hysteroscopy
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 21 Years to 45 Years (Adult) |
| Sexes Eligible for Study: | Female |
| Accepts Healthy Volunteers: | Yes |
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
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04512820
| Contact: Oshri Barel, MD | +927559382117 | Oshrib@assuta.co.il |
| Israel | |
| Assuta Ashdod University Hospital | Recruiting |
| Ashdod, Israel | |
| Contact: Oshri Barel, MD +972559382117 oshrib@assuta.co.il | |
| Principal Investigator: Oshri Barel, MD | |
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Assuta Ashdod Hospital |
| ClinicalTrials.gov Identifier: | NCT04512820 |
| Other Study ID Numbers: |
005-20-AAA |
| First Posted: | August 14, 2020 Key Record Dates |
| Last Update Posted: | August 14, 2020 |
| Last Verified: | July 2020 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | Undecided |
| Plan Description: | only unidentified data will be shared |
| 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 |
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Abortion, Spontaneous Pregnancy Complications |

