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Magnetic Resonance Guided Focused Ultrasound for Uterine Fibroids (PROMISe)

Primary Purpose

Uterine Fibroids

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
MR Guided Focused Ultrasound
Placebo MR Guided Focused Ultrasound
Sponsored by
University of California, San Francisco
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Uterine Fibroids focused on measuring Fibroids, Uterine, Focused Ultrasound, Magnetic Resonance focused ultrasound, HIFU, NOninvasive, Treatment

Eligibility Criteria

18 Years - 99 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Age>18 years
  • Premenopausal
  • Symptomatic fibroids
  • Fibroids accessible for focused ultrasound treatment

Exclusion criteria:

  • Desires future fertility
  • Current pregnancy
  • Hematocrit <30%
  • Emergency room visit in last 3 months for fibroid symptoms
  • History of venous thromboembolism
  • Fibroids that are: >10cm, non-enhancing with contrast
  • Adenomyosis
  • Contraindications to undergoing MRI
  • Unexplained menstrual irregularity

Sites / Locations

  • University of California, San Francisco

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

MR Guided Focused Ultrasound

Placebo MR Guided Focused Ultrasound

Arm Description

Outcomes

Primary Outcome Measures

Fibroid volume measured on MRI
Fibroid symptoms reported by participant
Red blood cell count (hematocrit)

Secondary Outcome Measures

Full Information

First Posted
June 15, 2011
Last Updated
November 4, 2019
Sponsor
University of California, San Francisco
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1. Study Identification

Unique Protocol Identification Number
NCT01377519
Brief Title
Magnetic Resonance Guided Focused Ultrasound for Uterine Fibroids
Acronym
PROMISe
Official Title
Magnetic Resonance-Guided Focused Ultrasound to Treat Uterine Fibroids: A Pilot Randomized, Placebo-Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
November 2019
Overall Recruitment Status
Completed
Study Start Date
June 2011 (undefined)
Primary Completion Date
September 2012 (Actual)
Study Completion Date
December 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of California, San Francisco

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a pilot randomized, blinded, placebo-controlled trial of a noninvasive, FDA approved treatment for uterine fibroids called MR Guided Focused Ultrasound (MRgFUS). Our hypothesis is that MRgFUS provides superior relief of fibroid symptoms compared with the placebo, a sham MRgFUS treatment. The investigators will recruit 20 premenopausal women with symptomatic uterine fibroids to participate in the trial. Participants will be randomly assigned in a 2:1 ratio to the active treatment arm (MRgFUS) versus the sham MRgFUS treatment. Participants will remain blinded to their group assignment for 3 months. After 3 months, participants will be told their treatment group and those assigned to the sham group will be offered complimentary MRgFUS if they desire it. Women will be excluded if they are inappropriate candidates for a 3 month delay in fibroid treatment, such as those with significant anemia. The investigators will assess the change from baseline to 1 and 3 months after treatment in fibroid symptoms, quality of life, fibroid volume measured by MRI, and hematocrit.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Uterine Fibroids
Keywords
Fibroids, Uterine, Focused Ultrasound, Magnetic Resonance focused ultrasound, HIFU, NOninvasive, Treatment

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
MR Guided Focused Ultrasound
Arm Type
Active Comparator
Arm Title
Placebo MR Guided Focused Ultrasound
Arm Type
Placebo Comparator
Intervention Type
Procedure
Intervention Name(s)
MR Guided Focused Ultrasound
Intervention Description
This is an FDA approved noninvasive treatment for fibroids that uses highly focused ultrasound waves to damage fibroid tissue.
Intervention Type
Procedure
Intervention Name(s)
Placebo MR Guided Focused Ultrasound
Intervention Description
This is a placebo treatment that requires a participant to undergo identical procedures as those of the actual MR Guided Focused Ultrasound procedure, but higly focused ultrasound waves are not directed at the uterine fibroid.
Primary Outcome Measure Information:
Title
Fibroid volume measured on MRI
Time Frame
Change from baseline prior to treatment until 3 months after treatment
Title
Fibroid symptoms reported by participant
Time Frame
Change from baseline prior to treatment to 1 and 3 months after treatment
Title
Red blood cell count (hematocrit)
Time Frame
Change from baseline prior to treatment and 3 months after treatment

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age>18 years Premenopausal Symptomatic fibroids Fibroids accessible for focused ultrasound treatment Exclusion criteria: Desires future fertility Current pregnancy Hematocrit <30% Emergency room visit in last 3 months for fibroid symptoms History of venous thromboembolism Fibroids that are: >10cm, non-enhancing with contrast Adenomyosis Contraindications to undergoing MRI Unexplained menstrual irregularity
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vanessa Jacoby, MD
Organizational Affiliation
University of California, San Francisco
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of California, San Francisco
City
San Francisco
State/Province
California
ZIP/Postal Code
94115
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
26658133
Citation
Jacoby VL, Kohi MP, Poder L, Jacoby A, Lager J, Schembri M, Rieke V, Grady D, Vittinghoff E, Coakley FV. PROMISe trial: a pilot, randomized, placebo-controlled trial of magnetic resonance guided focused ultrasound for uterine fibroids. Fertil Steril. 2016 Mar;105(3):773-780. doi: 10.1016/j.fertnstert.2015.11.014. Epub 2015 Dec 1.
Results Reference
derived
Links:
URL
https://clinicaltrials.ucsf.edu/fibroids
Description
Fibroid trials at UCSF

Learn more about this trial

Magnetic Resonance Guided Focused Ultrasound for Uterine Fibroids

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