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Vaginal Flora Imbalance clinical trials

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NCT ID: NCT06085898 Not yet recruiting - Clinical trials for Vaginal Flora Imbalance

Stryphnodendron Adstringens Intimate Soap

Start date: November 5, 2023
Phase: N/A
Study type: Interventional

This is a single-centre, single-blind, non-comparative clinical trial to assess the safety of the investigational product through clinical probability assessment. Thirty-three female participants, aged between 18-45, will be required. Assessment of dermal (dermatological) and gynecological acceptance, in addition to pH measurements and vaginal force collection for microbiological analysis at the beginning and end of the study.

NCT ID: NCT05850078 Recruiting - Clinical trials for Vaginal Flora Imbalance

FB101 Intervention in Women Screened to Have Vaginal Dysbiosis (Dyscover-3)

Dyscover-3
Start date: May 18, 2023
Phase: N/A
Study type: Interventional

This study will explore and map the potential shifts in vaginal microbiomes as a consequence of a microbial intervention with product FB101 in healthy, asymptomatic volunteer women screened to have vaginal dysbiosis based on criteria defined by quantitative polymerase chain reaction (qPCR) analysis of a vaginal swab sample.

NCT ID: NCT05808816 Recruiting - HPV Infection Clinical Trials

"Lactobacillus Crispatus M247, LSIL and Microbiota"

Start date: June 16, 2021
Phase: Phase 4
Study type: Interventional

Patients affected by ASC-US/ low-grade HPV cervical lesions will be randomly assigned to treatment arm vs control arm. The treatment arm will include the characterization of the vaginal microbiota at enrollment (T0), 4 months of oral treatment with Lactobacillus Crispatus M 247 (1 buccal stick Die), characterization of the vaginal microbiota at 1 month post treatment (T5 m). The vaginal microbiota will be evaluated by Danagene microbiome vaginal DNA KIT-XMICROGem (XBIOGem) test, with amplification of the variable regions of the 16S ribosomal RNA gene, using the MICROBIOTA kit (CE-IVD - ARROW diagnostics) and second generation sequencing technologies (NGS on Illumina MiSeq platform). The control arm will provide for the characterization of the vaginal microbiota at the same timescales. Patients will be given a medical history questionnaire at T0 and T5m

NCT ID: NCT05640700 Recruiting - Clinical trials for Human Papilloma Virus

Vaginal Microbiome and HPV Pre-malignant and Cervical Dysplasia

Start date: November 9, 2022
Phase:
Study type: Observational

In this study, the investigators will prospectively collect, analyze and integrate information regarding vaginal microbiome composition and HPV presence in women with cervical pathologies (high-grade CIN and CC) and controls, to construct a large dataset from patients with pre-cancerous cervical lesions and healthy women, to evaluate the personalized contribution of the vaginal microbiome to the CIN-CC sequence.

NCT ID: NCT05573334 Recruiting - Clinical trials for Urinary Tract Infections

Vaginal Care System for Menopausal Women With Urinary Tract Infections

Start date: July 10, 2023
Phase: N/A
Study type: Interventional

Menopausal women have an increased risk of recurrent urinary tract infections. This is likely due in part to hormonal changes occurring during menopause. As estrogen falls, the vaginal microbiome shifts from a healthy one to a less healthy one. Because the vagina is close to the urethra, this vaginal microbiome shift contributes to a loss of protection against urinary tract infections (UTIs). The investigators are asking whether improving the vaginal microbiome using an over-the-counter vaginal hygiene system can reduce frequency of recurrent UTI in menopausal women.

NCT ID: NCT05150639 Recruiting - Clinical trials for Vaginal Flora Imbalance

Vaginal Microbiome and IVF Pregnancy Outcome

Start date: March 18, 2022
Phase:
Study type: Observational

The aim of this prospective, observational study is to investigate the prevalence of vaginal dysbiosis among women undergoing IVF procedures in the US. And to investigate the associations between the vaginal microbiome and the pregnancy outcome following IVF.

NCT ID: NCT05114031 Completed - Clinical trials for Vaginal Flora Imbalance

FB101 Intervention in Women Screened to Have Vaginal Dysbiosis

DYSCOVER-1
Start date: October 20, 2021
Phase: N/A
Study type: Interventional

This study will explore and map the potential shifts in vaginal microbiomes as a consequence of a microbial intervention with product FB101 in healthy, asymptomatic volunteer women screened to have vaginal dysbiosis based on criteria defined by metagenomic sequencing of a vaginal swab sample.

NCT ID: NCT04721938 Completed - Infertility Clinical Trials

Healthy Parents - Healthy Children. Weight Loss Before Fertility Treatment

Start date: May 1, 2020
Phase: N/A
Study type: Interventional

The detrimental effect of overweight and obesity on fecundity has been well documented. The investigators wish to investigate the intervention program for weight loss before fertility treatment. Subsequently to gain knowledge on the effect of overweight/obesity and weight loss on the vaginal microbiome, on DNA damage on sperm cells, on the occurrence of endocrine disruptors in the endometrium, and on the gene expression in the endometrium.

NCT ID: NCT04658355 Not yet recruiting - Clinical trials for Vaginal Flora Imbalance

Chlorhexidine Gluconate Versus Povidone-iodine

CHDvPI
Start date: December 15, 2020
Phase: N/A
Study type: Interventional

A hysterectomy, or removal of the uterus, is a common surgery performed for a variety of reasons. During this surgery, to prevent infection, the vagina is thoroughly prepped with a cleansing solution, most commonly chlorhexidine gluconate or povidone-iodine. While studies have shown that chlorhexidine gluconate is better at killing bacteria people have raised concerns on how it affects the vaginal tissue. It is important to study these effects the cleansing solution surgeons use for this surgery can not only prevent infection but not cause harmful side effects.

NCT ID: NCT04202302 Recruiting - Clinical trials for Vaginal Flora Imbalance

Vaginal Profile in IVF/ICSI and Impact on Clincal Outcome

Start date: August 6, 2019
Phase:
Study type: Observational

Vaginal flora is closely related to female reproductive health. Previous studies have suggested that the composition of the vaginal flora is related to the pregnancy outcomes, and abnormalities in the vaginal flora lead to a decrease in the success rate of IVF. During the IVF treatment, the hormone level changes far exceed the physiological level. What changes will happen to the vaginal flora? Does IVF treatment itself affect the vaginal flora and affect outcomes? This study used prospective cohort study to show the changes in vaginal flora during conventional IVF treatment, providing more evidence for revealing the relationship between vaginal flora and infertility treatment outcomes.