Therapeutic Lactose to Support Vaginal Microbiota
Primary Purpose
Bacterial Vaginoses
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Lactose
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Bacterial Vaginoses
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.
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
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
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