The Accuracy of Ultrasound in the Detection of Placenta Site in the First Trimester.
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| ClinicalTrials.gov Identifier: NCT04579796 |
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Recruitment Status :
Suspended
(lack of funding)
First Posted : October 8, 2020
Last Update Posted : October 8, 2020
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Placenta; Implantation | Other: ultrasound exam Procedure: hysteroscopy diagnostic | Not Applicable |
| Study Type : | Interventional (Clinical Trial) |
| Estimated Enrollment : | 25 participants |
| Allocation: | N/A |
| Intervention Model: | Single Group Assignment |
| Masking: | None (Open Label) |
| Masking Description: | The performer of the hysteroscopy will not be aware of the result of the ultrasound exam |
| Primary Purpose: | Diagnostic |
| Official Title: | The Accuracy of Ultrasound in the Detection of Placenta Site in the First Trimester When Compared to Hysteroscopy in Early Abortions |
| Actual Study Start Date : | February 1, 2019 |
| Estimated Primary Completion Date : | October 1, 2020 |
| Estimated Study Completion Date : | December 30, 2020 |
| Arm | Intervention/treatment |
|---|---|
| Experimental: women with first trimester missed abortion |
Other: ultrasound exam
An abdominal ultrasound exam to assess the placenta implantation site. Procedure: hysteroscopy diagnostic Diagnostic hysteroscopy to asses the placenta implantation site. |
- The accuracy of placental site/ gestational sac implantation with ultrasound in the first trimester [ Time Frame: up to 12 weeks ]Transabdominal ultrasonography detection of gestational sac insertion location will be compared with gestational sac location diagnosed with hysteroscopy.
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| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | Female |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Healthy women .
- Clinical diagnosis of first trimester spontaneous abortion.
Exclusion Criteria:
- viable pregnancy
- women below 18 years
- women with chronic disease
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): NCT04579796
| Israel | |
| Asaf ha Rofeh, MC | |
| Zrifin, Israel, 70300 | |
| Responsible Party: | Assaf Harofeh MC, Doctor, Assaf-Harofeh Medical Center |
| ClinicalTrials.gov Identifier: | NCT04579796 |
| Other Study ID Numbers: |
# 0178-19 |
| First Posted: | October 8, 2020 Key Record Dates |
| Last Update Posted: | October 8, 2020 |
| Last Verified: | October 2020 |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |

