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Search / Trial NCT04415489

SIS Versus Office Hysteroscopy for Uterine Cavity Evaluation Prior to IVF

Launched by UNIVERSITY OF NORTH CAROLINA, CHAPEL HILL · Jun 1, 2020

Trial Information

Current as of April 29, 2025

Completed

Keywords

Assisted Reproduction

ClinConnect Summary

Saline infusion sonography (SIS) and hysteroscopy are commonly employed methods for uterine cavity evaluation. SIS is often performed as a screening tool in the office for uterine evaluation since it is straight-forward to perform, well-tolerated has low overhead cost. If uterine pathology is suspected on SIS, subsequent hysteroscopy is typically performed in the operating room. Hysteroscopy remains the gold standard for diagnosis of intra-uterine pathology and offers the opportunity for intervention at time of diagnosis, but often is not used as the initial screening tool because of provid...

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • Women aged 18 - 50
  • Patients undergoing routine cavity evaluation for planned in vitro-fertilization cycles
  • Exclusion Criteria:
  • Clinical or radiologic suspicion of intrauterine pathology including myomas, severe intrauterine adhesions or retained products of conception
  • Those with medical criteria not suitable office hysteroscopy due to requirement of advanced tools or preparation not available in the office such as history of bleeding disorder or medical co-morbidity

About University Of North Carolina, Chapel Hill

The University of North Carolina at Chapel Hill (UNC) is a leading research institution renowned for its commitment to advancing health and science through innovative clinical trials. With a robust infrastructure that supports multidisciplinary collaboration, UNC conducts cutting-edge research across various fields, including medicine, public health, and biomedical sciences. The university is dedicated to improving patient care and health outcomes by translating its research findings into practical applications. UNC’s clinical trials are designed to evaluate new therapies, interventions, and technologies, ensuring that they meet the highest ethical and scientific standards while fostering a culture of inclusivity and community engagement.

Locations

Raleigh, North Carolina, United States

Patients applied

0 patients applied

Trial Officials

Sarah Moustafa, MD

Principal Investigator

University of North Carolina, Chapel Hill

Linnea Goodman, MD

Study Chair

University of North Carolina, Chapel Hill

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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