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Clinical Trials/ACTRN12624000204549
ACTRN12624000204549RecruitingPhase 2

Pilot oral safety and efficacy of eucalypt sap resin for the management of recurrent vulvovaginal candidiasis (RVVC) and associated gastrointestinal symptoms: A comparative, 2-arm, double-blinded randomised study

Integria Healthcare (Australia) Pty Ltd.0 sites24 target enrollmentStarted: March 1, 2024Last updated:
Conditions

Trial Snapshot

Phase
Phase 2
Status
Recruiting
Enrollment
24

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional
Allocation
Randomised controlled trial
Primary Purpose
Prevention
Masking
Blinded (masking used)

Eligibility Criteria

Ages
18 Years to 65 Years (—)
Sex
Female

Inclusion Criteria

  • Females with medically diagnosed recurrent vulvovaginal candidiasis (RVVC); and gastrointestinal symptoms of candida overgrowth for a minimum of four weeks
  • - No serious current illnesses or specific chronic illness (per exclusion criteria)
  • - Participants must be on contraception, and those participants who choose to use hormonal contraception should be on stable levels at least 6 weeks prior to and during the trial
  • - Any prescription medication use by participants (other than that listed in exclusion criteria) must be stable for six weeks or more prior to trial
  • - Ability and willingness to collect vaginal swabs; - Females with medically diagnosed recurrent vulvovaginal candidiasis (RVVC); and gastrointestinal symptoms of candida overgrowth for a minimum of four weeks
  • - No serious current illnesses or specific chronic illness (per exclusion criteria)
  • - Participants must be on contraception, and those participants who choose to use hormonal contraception should be on stable levels at least 6 weeks prior to and during the trial
  • - Any prescription medication use by participants (other than that listed in exclusion criteria) must be stable for six weeks or more prior to trial
  • - Ability and willingness to collect vaginal swabs

Exclusion Criteria

  • - Pregnant, planning pregnancy or breastfeeding
  • - Not willing to use contraception for the duration of the study
  • - Taking warfarin or any other anti-coagulant medication, diabetic medication, corticosteroids, antibiotics, or immunosuppressive medications/treatments
  • - Diagnosed with cancer (if active within last five years and excepting skin cancer)
  • - Individuals diagnosed with significant chronic illness including inflammatory bowel disease, liver disorders, kidney disease, autoimmune disorders, pelvic inflammatory disease, cystitis, sexually transmitted infections (STI), or any other medically diagnosed vulvovaginal conditions (excepting RVVC)
  • - Treatment of any vaginal infection, STI or urinary tract infection within the last six weeks including the use of vaginal douches, pessaries, probiotics (including vaginal and oral administration) for any reason
  • - Use of corticosteroids or oral antibiotics for any condition within the last four weeks
  • - Use of any antifungal treatments regularly for control of RVVC, including medications (i.e., Nystatin or fluconazole) or herbal treatment (i.e., Pau D’arco or horopito). Probiotics are permissible providing the use is regular for four weeks or more and ongoing
  • - Currently unwell with acute infection or fever or having Covid-19 within the last four weeks
  • - In poor general health as assessed by Study Investigators; - Pregnant, planning pregnancy or breastfeeding
  • - Not willing to use contraception for the duration of the study
  • - Taking warfarin or any other anti-coagulant medication, diabetic medication, corticosteroids, antibiotics, or immunosuppressive medications/treatments
  • - Diagnosed with cancer (if active within last five years and excepting skin cancer)
  • - Individuals diagnosed with significant chronic illness including inflammatory bowel disease, liver disorders, kidney disease, autoimmune disorders, pelvic inflammatory disease, cystitis, sexually transmitted infections (STI), or any other medically diagnosed vulvovaginal conditions (excepting RVVC)
  • - Treatment of any vaginal infection, STI or urinary tract infection within the last six weeks including the use of vaginal douches, pessaries, probiotics (including vaginal and oral administration) for any reason
  • - Use of corticosteroids or oral antibiotics for any condition within the last four weeks
  • - Use of any antifungal treatments regularly for control of RVVC, including medications (i.e., Nystatin or fluconazole) or herbal treatment (i.e., Pau D’arco or horopito). Probiotics are permissible providing the use is regular for four weeks or more and ongoing
  • - Currently unwell with acute infection or fever or having Covid-19 within the last four weeks
  • - In poor general health as assessed by Study Investigators

Investigators

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