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Clinical Trials/NL-OMON41729
NL-OMON41729
Completed
Not Applicable

Validation study of a novel clinical algorithm in evaluating abnormal uterine bleeding using a Combination of Saline Infusion Sonohysterography (SIS) and endometrial brush biopsy (EMB). - SIS+EMB algorithm validation

Catharina-ziekenhuis0 sites200 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Abnormal uterine bleeding
Sponsor
Catharina-ziekenhuis
Enrollment
200
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational invasive

Investigators

Eligibility Criteria

Inclusion Criteria

  • \- Abnormal postmenopausal bleeding with a TED of \>4mm.
  • \- All women with abnormal postmenopausal bleeding will be informed about the study and asked to agree on participation, in case they do meet the 4mm TED criteria, before sonography is performed.

Exclusion Criteria

  • \- TED \<\=4mm
  • \- Suspected uterine infection
  • \- Suspected intrauterine abnormalities seen on first ultrasound
  • \- Pregnancy
  • \- Pathologic evidence of malignancy
  • \- Being incapacitated

Outcomes

Primary Outcomes

Not specified

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