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Laparoscopic Occlusion of Uterine Vessels Compared to Uterine Fibroid Embolization for Treatment of Uterine Fibroids

Primary Purpose

Uterine Fibroids

Status
Unknown status
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
Laparoscopic bilateral occlusion of uterine artery
Radiological embolization (UFE)
Sponsored by
Ullevaal University Hospital
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Uterine Fibroids focused on measuring uterine fibroids, leiomyoma, laparoscopy, menorrhagia

Eligibility Criteria

30 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria: Menorrhagia and/or bulk symptoms associated with uterine fibroids Exclusion Criteria: Malignancy Current or planned pregnancy Small submucous fibroids suitable for hysteroscopic resection Postmenopausal women Suspected or known adenomyosis Uterus size exceeding the umbilical level Contraindications against laparoscopic surgery

Sites / Locations

  • Ullevål University Hospital

Outcomes

Primary Outcome Measures

Reduction of menstrual bleeding six months after treatment measured by PBAC

Secondary Outcome Measures

Patient assessment of symptom reduction including menorrhagia and bulk symptoms
postoperative pain
recovering time
complications
failures
recurrence
secondary interventions
Reduction in fibroids and uterus size measured by ultrasonography and MRI

Full Information

First Posted
January 12, 2006
Last Updated
July 3, 2011
Sponsor
Ullevaal University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT00277680
Brief Title
Laparoscopic Occlusion of Uterine Vessels Compared to Uterine Fibroid Embolization for Treatment of Uterine Fibroids
Official Title
A Randomized Trial Comparing Laparoscopic Bilateral Occlusion of Uterine Vessels to Uterine Fibroid Embolization for the Treatment of Symptomatic Uterine Fibroids
Study Type
Interventional

2. Study Status

Record Verification Date
January 2006
Overall Recruitment Status
Unknown status
Study Start Date
December 2000 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
April 2010 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Ullevaal University Hospital

4. Oversight

5. Study Description

Brief Summary
Women with symptomatic uterine fibroids are treated either by Uterine Fibroid Embolization (UFE) or laparoscopic occlusion. The study hypothesis is that laparoscopic occlusion of uterine vessels and UFE have equal effect on bleeding symptoms. Menstrual bleeding reduction six months after treatment is the main endpoint. Secondary endpoints include participants assessment of symptom relief, and volume reduction of fibroids measured by MRI. We will also investigate possible differences in postoperative course, symptom reduction, complication, and recurrence. Patients are controlled with regular intervals up to five years after treatment.
Detailed Description
Uterine fibroid embolization (UFE)has become an alternative to hysterectomy for women with symptoms of uterine fibroids.Follow up studies of this new method have reported relief of menstrual bleeding by 85-90 % of the patients six to twelve months after treatment.Other studies have suggested laparoscopic bilateral occlusion of uterine arteries as an equal effective alternative, but to our knowledge there is no randomized studies published. Patients recruitment : Women with symptoms of uterine fibroids referred to the clinic,who express a desire to avoid hysterectomy. Study hypothesis: Laparoscopic occlusion of uterine vessels and UFE have equal effect on bleeding symptoms. Gynecological examination, ultrasonography and magnetic resonance imaging (MRI) are performed preoperatively and after 1,3 and 6 months. Clinical follow up is planned after 1,3,6,12,24,36 and 60 months.A validated bleeding chard, Pictorial Blood Assessment Chart(PBAC)is filled in by the participants during the last menstruation period before treatment and before each control. A standardized questionnaire to assess the bleeding amount,pressure symptoms, pain, adverse events, other complains and patients satisfaction is also used.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Uterine Fibroids
Keywords
uterine fibroids, leiomyoma, laparoscopy, menorrhagia

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (false)

8. Arms, Groups, and Interventions

Intervention Type
Procedure
Intervention Name(s)
Laparoscopic bilateral occlusion of uterine artery
Intervention Type
Procedure
Intervention Name(s)
Radiological embolization (UFE)
Primary Outcome Measure Information:
Title
Reduction of menstrual bleeding six months after treatment measured by PBAC
Secondary Outcome Measure Information:
Title
Patient assessment of symptom reduction including menorrhagia and bulk symptoms
Title
postoperative pain
Title
recovering time
Title
complications
Title
failures
Title
recurrence
Title
secondary interventions
Title
Reduction in fibroids and uterus size measured by ultrasonography and MRI

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
30 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Menorrhagia and/or bulk symptoms associated with uterine fibroids Exclusion Criteria: Malignancy Current or planned pregnancy Small submucous fibroids suitable for hysteroscopic resection Postmenopausal women Suspected or known adenomyosis Uterus size exceeding the umbilical level Contraindications against laparoscopic surgery
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Olav Istre, MD,PhD
Organizational Affiliation
Ullevål University Hospital, Dept.of Obstetrics and Gynecology
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Kirsten Hald, MD
Organizational Affiliation
Ullevål University Hospital, Dept of Obstetrics and Gynecology
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Nils-Einar Kløw, MD,PhD
Organizational Affiliation
Ullevaal University Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Ullevål University Hospital
City
Oslo
ZIP/Postal Code
0407
Country
Norway

12. IPD Sharing Statement

Citations:
PubMed Identifier
17197583
Citation
Hald K, Klow NE, Qvigstad E, Istre O. Laparoscopic occlusion compared with embolization of uterine vessels: a randomized controlled trial. Obstet Gynecol. 2007 Jan;109(1):20-7. doi: 10.1097/01.AOG.0000249602.39339.31.
Results Reference
derived

Learn more about this trial

Laparoscopic Occlusion of Uterine Vessels Compared to Uterine Fibroid Embolization for Treatment of Uterine Fibroids

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