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A Study to Compare the Effectiveness of Two Different Outpatient Endometrial Ablation Techniques Used for Heavy Periods (COAT)

Primary Purpose

Menorrhagia

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
NovaSure
thermachoice
Sponsored by
Birmingham Women's NHS Foundation Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Menorrhagia focused on measuring Heavy menstrual bleeding, menorrhagia, ThermachoiceTM, NovaSureTM, Endometrail Ablation

Eligibility Criteria

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

Inclusion Criteria:

  • Women with no desire to preserve their fertility who have heavy menstrual bleeding without organic pathology (DUB) of more than six months duration
  • Premenopausal follicular follicle stimulating hormone (FSH) level of less than 40 IU/L.
  • Associated functional disability (negative impact on life quality).
  • Lack of response to medical treatment.
  • Prepared to undergo surgical treatment without general anaesthesia

Exclusion Criteria:

  • Women under 25 years
  • Suspected genital tract infection
  • Uterine pathology including endometrial pathology on endometrial biopsy (e.g. endometrial hyperplasia or carcinoma) and structural lesions (e.g. uterine malformations, adhesions, polyps, submucous fibroids or extracavity fibroids > 3cm in diameter) as identified on pelvic ultrasound and/or outpatient hysteroscopy.
  • Uterine cavity length >11cm
  • Adnexal pathology
  • Previous open myomectomy or endometrial ablation / resection and classical caesarian section
  • patients considered vulnerable (e.g. current mental illness, emotionally labile, learning difficulties, immaturity)

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Other

    Arm Label

    novasure

    thermachoice

    Arm Description

    Bipolar radio-frequency energy ablation of the endometrium by thermal therapy under impedance control. The bipolar current generated by the device produces a tapered depth of ablation with shallower ablation in the cornual regions / lower uterine segment and a deeper ablation in the mid-body of the uterus..

    ThermachoiceTM III thermal balloon ablation

    Outcomes

    Primary Outcome Measures

    Amenorrhoea
    The objective of any treatment for HMB is to substantially reduce the amount of menstrual blood loss.Amenorrhoea rates are often chosen as the primary outcome measure in clinical trial of the effectiveness of endometrial ablation in women with HMB.

    Secondary Outcome Measures

    Visual analogue scale for assessment of pain
    The main limitation of outpatient interventions is the amount of pain generated. Endometrial ablation has been shown to be feasible and generally well tolerated in conscious patients in small observational series10-11, but direct randomised comparisons between techniques regarding the amount of pain experienced during surgery are lacking

    Full Information

    First Posted
    March 18, 2010
    Last Updated
    May 14, 2010
    Sponsor
    Birmingham Women's NHS Foundation Trust
    Collaborators
    Hologic, Inc.
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    1. Study Identification

    Unique Protocol Identification Number
    NCT01124357
    Brief Title
    A Study to Compare the Effectiveness of Two Different Outpatient Endometrial Ablation Techniques Used for Heavy Periods
    Acronym
    COAT
    Official Title
    A Randomised Control Trial To Compare the Effectiveness of Outpatient Endometrial Ablation Techniques (Novasure vs Thermachoice)in the Treatment of Menorhagia
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    May 2006
    Overall Recruitment Status
    Completed
    Study Start Date
    May 2006 (undefined)
    Primary Completion Date
    October 2007 (Actual)
    Study Completion Date
    October 2008 (Actual)

    3. Sponsor/Collaborators

    Name of the Sponsor
    Birmingham Women's NHS Foundation Trust
    Collaborators
    Hologic, Inc.

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    STUDY HYPOTHESIS: Does outpatient NovaSureTM endometrial ablation alleviate excessive menstrual bleeding and improve life quality more effectively than outpatient ThermachoiceTM endometrial ablation?
    Detailed Description
    Heavy menstrual bleeding (HMB) or 'menorrhagia' is a common condition with a major impact on health-related quality of life and health resource utilization in both primary and secondary care. In over 50% of cases no organic pathology is present and the term dysfunctional uterine bleeding (DUB) is used. First line treatment of DUB is medical and where this fails, surgery is indicated using either minimally invasive approaches (endometrial ablation) or major surgery (hysterectomy). Endometrial ablation has been extensively evaluated against the gold standard of hysterectomy and shown to be effective and associated with fewer complications. The technique involves destroying the entire, or a substantial proportion, of the endometrium thereby preventing cyclical endometrial regeneration and suppressing or reducing menstrual blood loss. Recent advances in endoscopic technology have resulted in the development of miniature, automated ablative systems (so called 'second generation devices'), which are easy to use, safe and obviate the need for routine unpleasant and expensive endometrial preparatory drugs10. Moreover, these devices have the potential to be routinely used in the outpatient or 'office' setting without the need for general anaesthesia. This approach is increasingly being advocated as it expands patient choice and potentially increasing safety and cost-effectiveness of treatment. The three most commonly employed and evaluated ablative devices are ThermachoiceTM III thermal balloon ablation (Gynecare Inc, Somerville, NJ, USA), Microwave endometrial ablation (Microsulis plc, Waterlooville, Hampshire, UK) and NovaSureTM impedance-controlled endometrial ablation (Cytyc, Marlborough, MA USA). All appear to have comparable efficacy when employed as an inpatient under general anaesthesia in terms of patient satisfaction and life quality although data on direct head to head comparisons of these procedures when performed in an outpatient environment are scarce. All techniques have been employed without the need for general anaesthesia11,16-19, but only ThermachoiceTM has been reported in an outpatient setting11, without the need for formal theatre facilities or conscious sedation. The Microwave technique necessitates significant dilatation of the cervix that limits its potential for use in an outpatient setting in contrast to ThermachoiceTM and NovaSureTM10. The newer NovasureTM system is more effective than ThermachoiceTM because inpatient studies report a higher rate of amenorrhoea (cessation of menstrual periods - 43% versus 8%). Moreover, NovaSureTM may be a better technique for use in conscious patients in an outpatient setting as it is a shorter procedure (1.5 versus 8 minutes) and associated with less post-operative pain16,19 but it does require a greater degree of potentially painful cervical dilatation10. There is thus a need for a randomised trial to compare the effectiveness and acceptability of ThermachoiceTM and NovaSureTM endometrial ablation in an outpatient setting for the treatment of menorrhagia.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Menorrhagia
    Keywords
    Heavy menstrual bleeding, menorrhagia, ThermachoiceTM, NovaSureTM, Endometrail Ablation

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Participant
    Allocation
    Randomized
    Enrollment
    81 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    novasure
    Arm Type
    Active Comparator
    Arm Description
    Bipolar radio-frequency energy ablation of the endometrium by thermal therapy under impedance control. The bipolar current generated by the device produces a tapered depth of ablation with shallower ablation in the cornual regions / lower uterine segment and a deeper ablation in the mid-body of the uterus..
    Arm Title
    thermachoice
    Arm Type
    Other
    Arm Description
    ThermachoiceTM III thermal balloon ablation
    Intervention Type
    Device
    Intervention Name(s)
    NovaSure
    Other Intervention Name(s)
    Bipolar radio-frequency energy ablation
    Intervention Description
    Bipolar radio-frequency energy ablation of the endometrium by thermal therapy under impedance control. The bipolar current generated by the device produces a tapered depth of ablation with shallower ablation in the cornual regions / lower uterine segment and a deeper ablation in the mid-body of the uterus..
    Intervention Type
    Device
    Intervention Name(s)
    thermachoice
    Other Intervention Name(s)
    Thermal balloon ablation
    Intervention Description
    ThermachoiceTM III thermal balloon ablation
    Primary Outcome Measure Information:
    Title
    Amenorrhoea
    Description
    The objective of any treatment for HMB is to substantially reduce the amount of menstrual blood loss.Amenorrhoea rates are often chosen as the primary outcome measure in clinical trial of the effectiveness of endometrial ablation in women with HMB.
    Time Frame
    6 months after the intervention.
    Secondary Outcome Measure Information:
    Title
    Visual analogue scale for assessment of pain
    Description
    The main limitation of outpatient interventions is the amount of pain generated. Endometrial ablation has been shown to be feasible and generally well tolerated in conscious patients in small observational series10-11, but direct randomised comparisons between techniques regarding the amount of pain experienced during surgery are lacking
    Time Frame
    24 hours

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    25 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Women with no desire to preserve their fertility who have heavy menstrual bleeding without organic pathology (DUB) of more than six months duration Premenopausal follicular follicle stimulating hormone (FSH) level of less than 40 IU/L. Associated functional disability (negative impact on life quality). Lack of response to medical treatment. Prepared to undergo surgical treatment without general anaesthesia Exclusion Criteria: Women under 25 years Suspected genital tract infection Uterine pathology including endometrial pathology on endometrial biopsy (e.g. endometrial hyperplasia or carcinoma) and structural lesions (e.g. uterine malformations, adhesions, polyps, submucous fibroids or extracavity fibroids > 3cm in diameter) as identified on pelvic ultrasound and/or outpatient hysteroscopy. Uterine cavity length >11cm Adnexal pathology Previous open myomectomy or endometrial ablation / resection and classical caesarian section patients considered vulnerable (e.g. current mental illness, emotionally labile, learning difficulties, immaturity)
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Justin Mr Clark, MD MRCOG
    Organizational Affiliation
    Birmingham Women's NHS Foundation Trust
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    25004347
    Citation
    Smith PP, Malick S, Clark TJ. Bipolar radiofrequency compared with thermal balloon ablation in the office: a randomized controlled trial. Obstet Gynecol. 2014 Aug;124(2 Pt 1):219-225. doi: 10.1097/AOG.0000000000000395.
    Results Reference
    derived
    PubMed Identifier
    21173651
    Citation
    Clark TJ, Samuel N, Malick S, Middleton LJ, Daniels J, Gupta JK. Bipolar radiofrequency compared with thermal balloon endometrial ablation in the office: a randomized controlled trial. Obstet Gynecol. 2011 Jan;117(1):109-118. doi: 10.1097/AOG.0b013e3182020401.
    Results Reference
    derived

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    A Study to Compare the Effectiveness of Two Different Outpatient Endometrial Ablation Techniques Used for Heavy Periods

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