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Endometrial aspiration before or after Saline Infusion Sonography (SIS) in case of abnormal uterine bleeding: effect on specimen quality

Endometrial aspiration before or after Saline Infusion Sonography (SIS) in case of abnormal uterine bleeding: effect on specimen quality

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN43875039
Enrollment
120
Registered
2007-06-27
Start date
2006-09-01
Completion date
Unknown
Last updated
2021-11-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Abnormal uterine bleeding, Saline Infusion Sonography (SIS), endometrial aspiration Urological and Genital Diseases Uterine bleeding

Interventions

Sponsors

Vrije University Medical Centre (VUMC) (The Netherlands)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with abnormal uterine bleeding.

Exclusion criteria

Exclusion criteria: 1. Pelvic Inflammatory Disease (PID) 2. Cervical cancer

Design outcomes

Secondary

MeasureTime frame
Reliability of video SIS-images. The SIS was performed in the same session and was recorded on video.

Primary

MeasureTime frame
Quality assessment of aspiration specimen by pathologist. Evaluation of the biopsy was performed by the pathologist immediately after taking the endometrial biopsy.

Countries

Netherlands

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026