An In-vitro Real-time System Based on Tissue Smears to Identify Malignancy During Hysteroscopic Procedure

Hillel Yaffe Medical Center

Status: Unknown

Conditions: Uterine Neoplasms; Uterine Cervical Neoplasm

Treatments: Procedure: Hysteroscopy; Device: Infrared Spectroscopy

Study type: Interventional

Funder types: Other

Identifiers

NCT03971032

HYMC-0098-18

Details and patient eligibility

About

The aim of the current study is to develop a near real-time system using infrared spectroscopy, that will evaluate the histological specimen that was removed from the uterine cavity during the hysteroscopy.

Enrollment: 300 estimated patients

Sex: Female

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients undergoing hysteroscopy

Exclusion criteria

• Pregnancy

Trial design

Primary purpose: Diagnostic

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

---

300 participants in 1 patient group

Women undergoing hysteroscopy

Other group

Description:

Women presenting with abnormal bleeding, abnormal cervical or uterine findings who have consented to undergo hysteroscopy

Treatment:

Procedure: Hysteroscopy

Device: Infrared Spectroscopy