Photoacoustic Endoscopy in Endometrial Cancer

The Washington University

Status and phase: Withdrawn; Early Phase 1

Conditions: Endometrial Cancer; Benign Neoplasm of Body of Uterus

Treatments: Device: Photoacoustic endoprobe; Procedure: Photoacoustic endoscopy

Study type: Interventional

Funder types: Other

Identifiers

NCT01498237

201102405

Details and patient eligibility

About

The purpose of this research study is to evaluate whether a new technology called intrauterine photoacoustic endoscopy (PAE) can be used to evaluate the inner lining of the uterus.

Full description

The investigators will evaluate whether this technology can be used and also try to obtain photoacoustic images and functional data (oxygen contents, blood vessel characteristics, etc) of the uterine lining to assess its appearance in women with and without cancer of the endometrium. Currently, it is difficult for physicians to know whether or not tumors of the endometrium have invaded and spread to other organs without performing an extended surgery called a staging operation (removal of the lymph nodes or glands that drain the uterus to assess under the microscope whether or not the cancer has spread). Our long term goal is to use this new photoacoustic (PA) technology to improve detection of occult metastatic disease. Occult disease is defined as tumor which cannot be seen without the use of imaging techniques. and possibly avoid the need of extended operations. All of this could result in better care for patients with endometrial cancer and other gynecologic problems.

Sex: Female

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Women diagnosed with benign gynecologic pathology (N=10) or biopsy proven endometrial cancer (N=10) who will undergo hysterectomy.
• Participants must be ≥ 18 years of age.
• Subjects of reproductive potential must have a negative pregnancy test prior to study photoacoustic endoscopy procedure and hysterectomy.
• Subjects must be able understand and willing to sign a written informed consent form.

Exclusion criteria

• Subjects with contraindications for general anesthesia or hysterectomy.
• Subjects with evidence of active pelvic inflammatory disease or purulent cervicitis.
• Subjects with prior endometrial ablation procedures.
• Gross tumoral involvement of the cervix or lower genital tract precluding cervical dilatation and endometrial sounding.

Trial design

Primary purpose: Diagnostic

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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0 participants in 1 patient group

Photoacoustic endoscopy

Experimental group

Description:

This is a one-arm, feasibility study to determine how well the experimental procedure photoacoustic endoscopy will evaluate the human endometrial cavity in vivo.

Treatment:

Procedure: Photoacoustic endoscopy

Device: Photoacoustic endoprobe