HOME Study: Hysteroscopic Office Myomectomy Evaluation

Not Applicable

Completed

• Conditions: Uterine Fibroids; Polyps
• Interventions: Device: Myomectomy

• Registration Number: NCT01152112
• Lead Sponsor: Hologic, Inc.

Brief Summary

The purpose of this study is to demonstrate safety and effectiveness of the MyoSure Tissue Removal System when used by community gynecologists in an office setting for the treatment of patients with symptomatic intrauterine polyps and submucosal fibroids.

Detailed Description

Approximately one hundred subjects will be enrolled in a randomized, comparative setting study conducted at 10-15 investigational sites. Sixty subjects will be randomized to undergo treatment in an office setting, and 40 subjects will be randomized to undergo treatment in a hospital or ambulatory surgical center (ASC) setting. Subjects will undergo a hysteroscopic tissue removal procedure to remove intrauterine polyps, type 0 fibroids, or type I fibroids. Saline infused sonohysterogram images (SIS) obtained at three months post treatment will be compared to pre-treatment images, to determine the percent reduction in target pathology volume. Additionally, subject self-reported pain scores (as rated on an 11 point scale) will compare pain occurring during the treatment procedure to the average pain level experienced during a PAP smear. Economic data will be collected and compared between the two treatment settings.

Study Timeline

• Study Start: 2010-06
• Study First Submitted: 2010-06-18
• Study First Submitted QC: 2010-06-25
• Study First Posted: 2010-06-29
• Primary Completion: 2012-01
• Study Completion: 2013-06
• Results First Submitted: 2014-09-10
• Status Verified: 2017-08
• Results First Submitted QC: 2017-08-09
• Last Update Submitted: 2017-08-09
• Results First Posted: 2017-09-13
• Last Update Posted: 2017-09-13

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 74

Inclusion Criteria

• Healthy female between 18 and 55 years of age

• Subject must be able to understand, read and sign the study specific informed consent forms after the nature of the study has been fully explained to her

• Subject is a pre-menopausal or peri-menopausal female, either nulliparous or parous

• Subject is experiencing AUB as confirmed by a symptom raw score of 23 or a calculated symptom score of 44.0 or higher on the Uterine Fibroid Scale and Health Related Quality of Life (UFS-QOL)

• Subject is indicated for myomectomy or polypectomy for benign appearing pathology, based on a hysteroscopic exam and measured by saline infused sonogram assessment within 30 days of the planned index procedure

• Subject exhibits intrauterine polyps and/or submucous myomas which, in the opinion of the treating physician, are compatible with office-based treatment (e.g. 15 minutes or less of cutting time) using the MyoSure device and meet at least one of the following criteria:

• One or more polyps, with at least one of the polyps ≥ 1.5 cm and ≤ 3.0 cm diameter and having broad based attachment to the uterine wall.

• Up to two Type 0 or Type 1 myomas with at least one of the myomas being ≥ 1.5 cm and none of the myomas being 3.0 cm diameter

  • If the first myoma is 3.0 cm, the second myoma must be ≤ 2.0 cm
  • Fundal myomas must be Type 0

• Polyps plus up to two Type 0 or Type I myomas with at least one of the myomas being ≥ 1.5cm and ≤ 3.0 cm

• The subject demonstrates a negative pregnancy test within 48 hours prior to the planned index procedure

• The subject must document a score of 5 or lower on the Pap Smear and Blood Draw scales of the Pain Tolerance Survey

Exclusion Criteria

• Subject has known or suspected cancer, including breast, endometrial, and ovarian

• Contraindication and/or allergy to local anesthetic, or oral medications specified in the treatment protocol

• The subject has a history of chronic narcotic use

• Previous uterine artery embolization or other uterine artery occlusion procedure (Doppler or laparoscopic)

• Subject has blood borne pathogens-HIV, hepatitis B, CJD, etc.

• Subject has an IUD at the time of the procedure. A subject may be enrolled in the study if the IUD is removed prior to the treatment procedure

• Subject is taking an anticoagulant or antiplatelet medication other than low dose aspirin

• Active pelvic inflammatory disease or pelvic/vaginal infection

• Subject has a known or suspected coagulopathy or bleeding disorder

• Subject has a history of unmanaged endocrine disease

• Subject has current or past, acute or chronic psychiatric disorder which, in the opinion of the Investigator, may preclude proper evaluation and follow-up

• Subject has a history of auto-immune, inflammatory, or connective tissue disease

• Subject has a history of disease which increases the risk for fluid overload (i.e. significant cardiac, hepatic, or renal dysfunction)

• Uncontrolled hypertension lasting two years or more

• Use of any experimental drug or device within 30 days prior to the screening visit

• The subject has a terminal illness that may prevent the completion of any follow-up assessments

• Any employee or relative of an employee of the Sponsor company or any Investigator site employee or relative of employees working on the study

• Subject has other co-morbid condition(s) that, in the opinion of the Investigator, could limit the subject's ability to participate in the study or impact the scientific integrity of the study

• Subject has one of the following:

  • Type II submucosal myoma
  • Type O or Type I submucosal myoma > 3.0 cm
  • Fundal Type I myoma
  • Highly vascularized myoma as determined by SIS or hysteroscopic examination

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Treatment, Office Setting, myomectomy	Myomectomy	Myomectomy for uterine polyps and/or fibroids occurring in an office setting
Treatment, Hospital Setting, myomectomy	Myomectomy	Myomectomy for uterine polyps and/or fibroids occurring in a hospital setting

Primary Outcome Measures

Name	Time	Method
Percent Reduction in Target Pathology Volume	Three months post treatment	Percent reduction in target pathology volume, compared between pre-treatment baseline and 3 months post MyoSure treatment

Secondary Outcome Measures

Name	Time	Method
Percent of Subjects That Achieve 100% Removal of Target Pathology	Three months post treatment	Percent volume reduction of target pathology between baseline and month three post treatment assessments, as measured by saline infused sonohysterogram.
Subject Self-reported Pain Score Occurring During the Treatment Procedure	1 hour post treatment	Mean difference in pain score compared between subject-rated assessment of pain occurring during a pap smear and pain occurring during the MyoSure treatment procedure, based on the Wong-Baker Faces Rating Scale (FRS)

Trial Locations

Locations (9)

Boulder Women's Clinic; 🇺🇸 Boulder, Colorado, United States

Women's Health Care Practice; 🇺🇸 Champaign, Illinois, United States

Rubino OB/Gyn; 🇺🇸 West Orange, New Jersey, United States

Complete Healthcare for Women; 🇺🇸 Columbus, Ohio, United States

Obstetrics and Gynecology; 🇺🇸 North Charleston, South Carolina, United States

The Research Division for Integrated Health Services; 🇺🇸 Ann Arbor, Michigan, United States

Phoenix Gynecology Consultants; 🇺🇸 Phoenix, Arizona, United States

Kulbresh Women's Center; 🇺🇸 Irmo, South Carolina, United States

Williams, Benavides, Marston, & Kaminski; 🇺🇸 Raleigh, North Carolina, United States