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Baclofen/Diazepam Supps for Treatment of Pelvic Floor Myalgia (BDS)

Primary Purpose

Pelvic Floor Dyssynergia

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Baclofen/diazepam
Vaginal placebo
Sponsored by
Dr. John A. Thiel Medical Professional Corporation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pelvic Floor Dyssynergia

Eligibility Criteria

18 Years - 50 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Patients with significant pelvic floor dyssynergia and pain during sexual activity.

Exclusion Criteria:

  • Decide you do not wish to participate
  • Are pregnant
  • Have active pelvic inflammatory disease
  • Have an active sexually transmitted infection (STI)
  • Have a known or suspected cancer of the genital tract
  • Have untreated or unevaluated changes in your Pap smear
  • Are not currently sexually active
  • Have an allergy to either baclofen or valium
  • Are unable to complete the necessary study questionnaires

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Placebo Comparator

    Arm Label

    Vaginal Baclofen/diazepam supp

    Vaginal Placebo supp

    Arm Description

    Insert vaginal suppository once daily

    Insert vaginal suppository once daily

    Outcomes

    Primary Outcome Measures

    Change in Visual Analogue Scale for Pain (VAS-P) scores before and after treatment
    The scale ranges from 0 (no pain) to 10 (worst pain ever experienced)

    Secondary Outcome Measures

    Change in Female Sexual Function Index (FSFI)
    Self report measure of female sexual dysfunction
    Patient Global Impression of Improvement (PGI-I)
    Ranks patients overall feeling about health from 1 (very much better) to 7 (very much worse)
    Short form Health Survey (SF-12)
    Standardized self assessment tool to measure overall health status

    Full Information

    First Posted
    January 26, 2018
    Last Updated
    June 5, 2018
    Sponsor
    Dr. John A. Thiel Medical Professional Corporation
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03427216
    Brief Title
    Baclofen/Diazepam Supps for Treatment of Pelvic Floor Myalgia
    Acronym
    BDS
    Official Title
    A Randomized Double Blind Placebo Controlled Cross-over Trial of Baclofen and Diazepam Suppositories for the Management of Pelvic Floor Myalgia
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    June 2018
    Overall Recruitment Status
    Unknown status
    Study Start Date
    September 1, 2018 (Anticipated)
    Primary Completion Date
    December 31, 2018 (Anticipated)
    Study Completion Date
    December 31, 2018 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Dr. John A. Thiel Medical Professional Corporation

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    This study is a randomized, placebo controlled double blind cross over trial. Patients presenting with pelvic floor myalgia will be asked to complete a series of standardized questionnaires to assess their pain, quality of life and sexual function and satisfaction. They will be randomized to either a treatment group or placebo group and will use the supplied suppositories once daily for 2 months. They will then undergo a one month "washout" after which they will be placed in the cross over group for a second two months of treatment. Primary outcome measure: change in Visual Analogue Scale for Pain (VAS-P) scores before and after treatment Secondary outcome measures: change in Female Sexual Function Index (FSFI), Patient Global Impression of Improvement (PGI-I), and Short Form Health Survey (SF-12) before and after treatment
    Detailed Description
    Chronic pelvic pain is a complex multi-faceted problem that places a substantial burden on the healthcare resources. In Canada, the average hospital related cost for women requiring surgery or inpatient admission for chronic pelvic pain is $25 million each year. Chronic pelvic pain is defined as either persistent pain for at least 6 months or "recurrent episodes of abdominal/pelvic pain, hypersensitivity, or discomfort, often associated with elimination changes and sexual dysfunction in the absence of an organic etiology." Chronic pelvic pain is common and affects women of all ages and backgrounds. 15-20% of women have chronic pelvic pain lasting for more than 1 year. Pelvic floor myalgia is an important and common contributor to chronic pelvic pain that may be present alone or may co-exist with other gynecological, urological, colorectal, and musculoskeletal medical conditions. The International Urogynecological Association/International Continence Society joint report published in February 2017 defines pelvic floor myalgia as pain in the musculature of the pelvic floor.6 Patients with high-tone pelvic floor dysfunction (HTPFD) have levator hypercontractility and present with pain with internal vaginal examination and intercourse. In a 2011 prospective cross-sectional study by Fitzgerald et al., 63% of patients with self-reported chronic pelvic pain examined by a physician and 73.7% of patients examined by a physiotherapist were found to have pelvic floor myalgia. Although pelvic floor myalgia is a common condition encountered in gynecology, it is frequently an unrecognized and under-treated component of chronic pelvic pain. Pelvic floor myalgia has a significant impact on the patient's quality of life. Persistent chronic pain may result in patient's anxiety, low mood, depression, sleep disturbances, feeling of hopelessness and helplessness, frustration, and psychological distress. The first line of treatment for pelvic floor myalgia is pelvic floor muscle relaxation. Reducing the resting tone of pelvic floor musculature has been shown to improve chronic pelvic pain. Current treatment options for pelvic floor myalgia include pelvic floor physiotherapy, Thiele massage, biofeedback with electrical stimulation, behavioural modifications, acupuncture, medications such as antidepressants,1 trigger point injections with botulin A toxin, warm sitz baths, and neuromodulation. Recently, intravaginal diazepam has been used an off-label treatment option for high-tone pelvic floor myalgia. Diazepam is a benzodiazepine derivative that has both antispasmotic and anxiolytic activity. It is used as a muscle relaxant and enhances the inhibitory action of gamma-amino butyric acid (GABA) on neuronal excitability, resulting in decreased action potentials. The benefit of local therapy is the avoidance of the common side effects of benzodiazepines such as drowsiness, fatigue, and ataxia. Currently, evidence is lacking in regards to the effectiveness of intravaginal diazepam on treatment of chronic pelvic pain. The 2010 retrospective chart review of 26 patients by Rogalski et al. revealed clinically significant reduction in Visual Analogue Scale for Pain (VAS-P) and Female Sexual Function Index (FSFI) with diazepam suppositories used for 30 days as an adjuvant therapy to pelvic floor physiotherapy and intramuscular trigger point injections. Similarly, the 2011 study revealed 62% improvement in symptoms with intravaginal diazepam. Baclofen is a skeletal muscle relaxant. It is a GABA-B receptor agonist which is commonly used for treating spasticity. The literature on topical baclofen use in pelvic floor dysfunction is minimal. Topical therapy is advantageous to avoid the common systemic side effects such as drowsiness, hypotonia, hypotension, and headache. A retrospective study examining the use of topical baclofen for provoked vulvodynia showed an improvement in pain and sexual function. Baclofen may also be used in combination with diazepam for treatment of pelvic floor myalgia. A 2016 retrospective chart review performed at the University of Saskatchewan revealed a reduction in both dyspareunia and pelvic floor muscle spasm with the use of baclofen and diazepam vaginal suppositories.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Pelvic Floor Dyssynergia

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Crossover Assignment
    Masking
    ParticipantCare ProviderInvestigatorOutcomes Assessor
    Allocation
    Randomized
    Enrollment
    60 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Vaginal Baclofen/diazepam supp
    Arm Type
    Active Comparator
    Arm Description
    Insert vaginal suppository once daily
    Arm Title
    Vaginal Placebo supp
    Arm Type
    Placebo Comparator
    Arm Description
    Insert vaginal suppository once daily
    Intervention Type
    Drug
    Intervention Name(s)
    Baclofen/diazepam
    Other Intervention Name(s)
    Lioresal
    Intervention Description
    Vaginal suppository placed once daily, patients will record pelvic pain daily on a VAS scale, sexual satisfaction and quality of life on a standardized questionnaire weekly
    Intervention Type
    Drug
    Intervention Name(s)
    Vaginal placebo
    Other Intervention Name(s)
    suppository
    Intervention Description
    Vaginal suppository placed once daily, patient will record pelvic pain daily on a VAS scale, sexual satisfaction and quality of life on a standardized questionnaire weeky.
    Primary Outcome Measure Information:
    Title
    Change in Visual Analogue Scale for Pain (VAS-P) scores before and after treatment
    Description
    The scale ranges from 0 (no pain) to 10 (worst pain ever experienced)
    Time Frame
    5 months
    Secondary Outcome Measure Information:
    Title
    Change in Female Sexual Function Index (FSFI)
    Description
    Self report measure of female sexual dysfunction
    Time Frame
    5 months
    Title
    Patient Global Impression of Improvement (PGI-I)
    Description
    Ranks patients overall feeling about health from 1 (very much better) to 7 (very much worse)
    Time Frame
    5 months
    Title
    Short form Health Survey (SF-12)
    Description
    Standardized self assessment tool to measure overall health status
    Time Frame
    5 months

    10. Eligibility

    Sex
    Female
    Gender Based
    Yes
    Gender Eligibility Description
    46XX women
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    50 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Patients with significant pelvic floor dyssynergia and pain during sexual activity. Exclusion Criteria: Decide you do not wish to participate Are pregnant Have active pelvic inflammatory disease Have an active sexually transmitted infection (STI) Have a known or suspected cancer of the genital tract Have untreated or unevaluated changes in your Pap smear Are not currently sexually active Have an allergy to either baclofen or valium Are unable to complete the necessary study questionnaires

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    IPD Sharing Plan Description
    only pooled data will be shared outside of the research team

    Learn more about this trial

    Baclofen/Diazepam Supps for Treatment of Pelvic Floor Myalgia

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