search
Back to results

Therapeutic Lactose to Support Vaginal Microbiota

Primary Purpose

Bacterial Vaginoses

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Lactose
Placebo
Sponsored by
Peter Humaidan
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bacterial Vaginoses

Eligibility Criteria

18 Years - 60 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Amsel criteria positive defined as 3/4 of the following: Vaginal discharge, Fishy odor, pH>4.5 and Clue cells in a wet smear.

Exclusion Criteria:

  • Not able to provide written informed consent.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Placebo Comparator

    Arm Label

    Lactose

    Placebo

    Arm Description

    Lactose monohydrate 810 mg, silicon dioxide 20 mg, and magnesium stearate 14 mg

    Dextran 40 EP 671 mg, silicon dioxide 20 mg and magnesium stearate 14 mg

    Outcomes

    Primary Outcome Measures

    Bacterial load after intervention
    quantitative measurements with qPCR for G. vaginalis, Prevotella spp., A. vaginae, Megasphaera type 1, L. gasseri, L. crispatus, L. jensenii and L. iners after intervention

    Secondary Outcome Measures

    Full Information

    First Posted
    March 14, 2019
    Last Updated
    March 18, 2019
    Sponsor
    Peter Humaidan
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT03878511
    Brief Title
    Therapeutic Lactose to Support Vaginal Microbiota
    Official Title
    Effect of Vaginal Lactose on the Vaginal Microbiota in Women With Bacterial Vaginosis: Double-blind, Placebo-controlled Randomised Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2019
    Overall Recruitment Status
    Completed
    Study Start Date
    November 1, 2012 (Actual)
    Primary Completion Date
    March 1, 2013 (Actual)
    Study Completion Date
    March 1, 2013 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor-Investigator
    Name of the Sponsor
    Peter Humaidan

    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
    The aim of the study was to investigate whether the administration of a vaginal tablet containing lactose can modulate the bacterial flora of women with bacterial vaginosis (BV). Design: Double-blind, placebo-controlled randomised trial. Setting: Women with BV who responded to advertisements in local newspapers and on posters at the Institutions for Education in Health Science in Eastern Jutland, Denmark. These individuals were supplemented with patients enrolled at a gynaecological clinic. Participants: Forty women with BV diagnosed through the Amsel test. By randomisation, 20 were assigned to receive lactose tablets, and 20 were assigned to receive placebo tablets. Interventions: Twice daily application of one lactose tablet or placebo tablet for 7 days.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Bacterial Vaginoses

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantCare ProviderInvestigator
    Masking Description
    Active and inactive tablets were identical. The tablets were packed and labelled by the manufacturer. The key to identity was retained and was disclosed after recruiting all patients. After informed consent, eligible patients drew a closed opaque envelope from a set of envelopes numbered 1-40 and placed in random order. The envelope contained both number labels for medical data-related documents and sample vials and a closed opaque container holding tablets labelled with the sample number.
    Allocation
    Randomized
    Enrollment
    40 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Lactose
    Arm Type
    Experimental
    Arm Description
    Lactose monohydrate 810 mg, silicon dioxide 20 mg, and magnesium stearate 14 mg
    Arm Title
    Placebo
    Arm Type
    Placebo Comparator
    Arm Description
    Dextran 40 EP 671 mg, silicon dioxide 20 mg and magnesium stearate 14 mg
    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    Lactose
    Intervention Description
    Lactose monohydrate 810 mg, silicon dioxide 20 mg, and magnesium stearate 14 mg
    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    Placebo
    Intervention Description
    Dextran 40 EP 671 mg, silicon dioxide 20 mg and magnesium stearate 14 mg
    Primary Outcome Measure Information:
    Title
    Bacterial load after intervention
    Description
    quantitative measurements with qPCR for G. vaginalis, Prevotella spp., A. vaginae, Megasphaera type 1, L. gasseri, L. crispatus, L. jensenii and L. iners after intervention
    Time Frame
    7 days

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    60 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Amsel criteria positive defined as 3/4 of the following: Vaginal discharge, Fishy odor, pH>4.5 and Clue cells in a wet smear. Exclusion Criteria: Not able to provide written informed consent.

    12. IPD Sharing Statement

    Learn more about this trial

    Therapeutic Lactose to Support Vaginal Microbiota

    We'll reach out to this number within 24 hrs