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Reducing Abundance of Human Papilloma Virus in Women by Taking Probiotic

Primary Purpose

Human Papilloma Virus Infection

Status
Recruiting
Phase
Phase 2
Locations
Malaysia
Study Type
Interventional
Intervention
probiotic
placebo
Sponsored by
Universiti Sains Malaysia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Human Papilloma Virus Infection focused on measuring probiotics, human papilloma virus

Eligibility Criteria

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

Inclusion Criteria:

  • Sexually active women
  • Age above 26 years old
  • Determined as HPV positive against L1 variant
  • Willing to commit throughout the experiment

Exclusion Criteria:

  • On long term medication (6 months and above) for any illnesses
  • Pregnant
  • Uterus and/or cervix removed
  • Prior HPV vaccination
  • Cervical intraepithelial neoplasia

Sites / Locations

  • Hospital Seberang JayaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

probiotic 9 log CFU/day

placebo

Arm Description

Intervention consists of daily oral administration of one sachet/day of probiotic for 12 weeks, where each sachet contains 9 log CFU of probiotic.

placebo contains primarily carrier without probiotic and it is identical in taste and appearance and appear as light-yellow powder. It is also taken by the participants for 12 weeks.

Outcomes

Primary Outcome Measures

Changes in vaginal abundance of HPV of women upon administration of probiotic.
Differences in vaginal HPV abundance in women upon administration of probiotic at 9 log CFU/day compared to placebo via real-time PCR quantification of the L1 capsid gene as a conserved region of the HPV genome using consensus primers PGMY09 and PGMY1.

Secondary Outcome Measures

Changes in vaginal microbiota of women upon administration of probiotic.
Differences in vaginal microbiota in women upon administration of probiotic at 9 log CFU/day compared to placebo via microbiota profiling using DNA of vaginal samples amplified for bacterial 16S rRNA and analyzed for high-throughput community sequencing.
Changes in gut microbiota of women upon administration of probiotic.
Differences in gut microbiota profiles of women on probiotic and placebo via microbiota profiling using DNA of fecal samples amplified for bacterial 16S rRNA and analyzed for high-throughput community sequencing.
Changes in vaginal health of women upon administration of probiotic via the use of questionnaire.
Differences in total scores of women upon administration of probiotic at 9 log CFU/day compared to placebo via the use of vulvovaginal symptom questionnaire (VSQ) containing 21-items on a two-point scale with higher scores indicating poorer health status.
Changes in immunity of women upon administration of probiotic 9 log CFU/day as assessed via biochemical tests.
To evaluate differences in immunity of women on probiotic and placebo in terms of blood immunity profiling via measuring concentrations of immunoglobulins such as IgA, IgG and IgM, and cytokines such as interleukin (IL)-1b, IL-4, IL-10, TNF-α and IFN-γ using commercially available ELISA kits.

Full Information

First Posted
March 17, 2022
Last Updated
May 8, 2023
Sponsor
Universiti Sains Malaysia
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1. Study Identification

Unique Protocol Identification Number
NCT05316064
Brief Title
Reducing Abundance of Human Papilloma Virus in Women by Taking Probiotic
Official Title
The Effects of Probiotic Against Reducing Abundance of Human Papilloma Virus (HPV) in Women
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
December 27, 2021 (Actual)
Primary Completion Date
November 28, 2023 (Anticipated)
Study Completion Date
November 28, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universiti Sains Malaysia

4. Oversight

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

5. Study Description

Brief Summary
The purpose of this study is to evaluate the efficacy of oral administration of probiotic at 9 log colony forming unit (CFU)/day to reduce vaginal abundance of HPV in women compared to placebo via the use of vaginal self-swab.
Detailed Description
Probiotics have shown an antiviral activity and several mechanisms have been demonstrated. In respiratory tract infections (RTIs), the majority of probiotics can inhibit the most important respiratory viruses by immunomodulatory mechanisms. There are over 200 different types of viruses, which cause RTIs in humans. Human rhinoviruses (HRV) are the largest group of respiratory viruses, comprising over 150 serotypes. In humans, the predominant illness caused by HRV is the acute upper RTI, also known as the common cold. The second most common viruses infecting humans are the human enteroviruses (HEV), which are associated with clinical manifestations ranging from mild respiratory symptoms to serious conditions. Influenza viruses, respiratory syncytial virus (RSV), and adenoviruses are also major causative agents of both upper and lower RTIs. In addition, many other viruses or virus groups cause RTIs, e.g., parainfluenza viruses and coronaviruses can cause a broad spectrum of respiratory diseases, ranging from mild upper RTIs to pneumonia. In recent years, with the rapid development of high-throughput molecular techniques, several new viruses associated with respiratory diseases, such as human bocavirus, human metapneumovirus, and the new coronaviruses HKU1 and NL63, have been identified as well. Recently, COVID-19 had cause huge effect worldwide. With this, to reduce the burden and severity of this pandemic, the use of probiotic in preventing of COVID-19 has been ongoing. Probiotics also had given out significant outcome in gastroenteritis infections where a study suggested that probiotics had be effective in alleviating the duration and severity of acute rotavirus gastroenteritis. Apart from this, for viruses that cause hepatitis, skin virus infections, human immunodeficiency virus (HIV), or HPV, probiotics could directly or indirectly, help reduce their symptoms or prevent infection. Probiotics are known as a good natural non-drug, which was widely used to boost immune cells in host to fight against infection. Generally, probiotic effects are mediated through immune regulation, particularly through balance control of proinflammatory and anti-inflammatory cytokines. The immune response is initiated by innate immunity following exposure to foreign substances or tissue injury. Innate immunity exerts protective roles in host homeostasis in part by priming adaptive immune responses against persisting insults and inducing inflammation. However, the unbalanced immune response leads to severe inflammation and uncontrolled tissue damage and disease. Probiotics have been found to enhance the innate immunity and modulate pathogen-induced inflammation via toll-like receptor-regulated signaling pathways.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Human Papilloma Virus Infection
Keywords
probiotics, human papilloma virus

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
126 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
probiotic 9 log CFU/day
Arm Type
Experimental
Arm Description
Intervention consists of daily oral administration of one sachet/day of probiotic for 12 weeks, where each sachet contains 9 log CFU of probiotic.
Arm Title
placebo
Arm Type
Placebo Comparator
Arm Description
placebo contains primarily carrier without probiotic and it is identical in taste and appearance and appear as light-yellow powder. It is also taken by the participants for 12 weeks.
Intervention Type
Biological
Intervention Name(s)
probiotic
Intervention Description
oral administration of probiotic at 9 log CFU/day for 12 weeks to reduce vaginal abundance of HPV in women compared to placebo via the use of vaginal self-swab.
Intervention Type
Other
Intervention Name(s)
placebo
Intervention Description
oral administration of primarily carrier without the probiotic for 12 weeks
Primary Outcome Measure Information:
Title
Changes in vaginal abundance of HPV of women upon administration of probiotic.
Description
Differences in vaginal HPV abundance in women upon administration of probiotic at 9 log CFU/day compared to placebo via real-time PCR quantification of the L1 capsid gene as a conserved region of the HPV genome using consensus primers PGMY09 and PGMY1.
Time Frame
12-weeks
Secondary Outcome Measure Information:
Title
Changes in vaginal microbiota of women upon administration of probiotic.
Description
Differences in vaginal microbiota in women upon administration of probiotic at 9 log CFU/day compared to placebo via microbiota profiling using DNA of vaginal samples amplified for bacterial 16S rRNA and analyzed for high-throughput community sequencing.
Time Frame
12-weeks
Title
Changes in gut microbiota of women upon administration of probiotic.
Description
Differences in gut microbiota profiles of women on probiotic and placebo via microbiota profiling using DNA of fecal samples amplified for bacterial 16S rRNA and analyzed for high-throughput community sequencing.
Time Frame
12-weeks
Title
Changes in vaginal health of women upon administration of probiotic via the use of questionnaire.
Description
Differences in total scores of women upon administration of probiotic at 9 log CFU/day compared to placebo via the use of vulvovaginal symptom questionnaire (VSQ) containing 21-items on a two-point scale with higher scores indicating poorer health status.
Time Frame
12-weeks
Title
Changes in immunity of women upon administration of probiotic 9 log CFU/day as assessed via biochemical tests.
Description
To evaluate differences in immunity of women on probiotic and placebo in terms of blood immunity profiling via measuring concentrations of immunoglobulins such as IgA, IgG and IgM, and cytokines such as interleukin (IL)-1b, IL-4, IL-10, TNF-α and IFN-γ using commercially available ELISA kits.
Time Frame
12-weeks

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
26 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Sexually active women Age above 26 years old Determined as HPV positive against L1 variant Willing to commit throughout the experiment Exclusion Criteria: On long term medication (6 months and above) for any illnesses Pregnant Uterus and/or cervix removed Prior HPV vaccination Cervical intraepithelial neoplasia
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
MingTze Liong, PhD
Phone
+60175938806
Email
liongmintze@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
MingTze Liong, Doctor
Organizational Affiliation
School of Industrial Technology USM
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Binti Sany Salina, Doctor
Organizational Affiliation
Institut Perubatan & Pergigian Termaju USM
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Seberang Jaya
City
Pulau pinang
State/Province
Penang
ZIP/Postal Code
13700
Country
Malaysia
Individual Site Status
Recruiting
Facility Contact:
Phone
+60-04-3827224
Email
ppcpenang@moh.gov.my

12. IPD Sharing Statement

Plan to Share IPD
No

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Reducing Abundance of Human Papilloma Virus in Women by Taking Probiotic

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