The LISA (Lactoferrin InStead of Antibiotics/Antifungals) Feasibility Study
Recruiting
N/A
Interventional Study
Bacterial Vaginosis
Candida Vaginal
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 16 – 50
- Sex
- Female
- Study type
- Interventional
- Purpose
- Health Services Research
- Participants needed
- 114 (estimated)
- Sponsor
- Guy's and St Thomas' NHS Foundation Trust · Other
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About This Trial
Three-quarters of women have bacterial vaginosis (BV) or vaginal thrush/candida yeast infection at least once during their lifetime. Symptoms can include abnormal vaginal discharge, soreness, itching and an unpleasant smell. BV during pregnancy can make the baby come too early. In the UK over a million women suffer recurrent vaginal infections. These can affect their sexual relationships and quali…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Aged 16-49 years
* Having periods (apart from women with a Mirena IUCD or polycystic ovary syndrome)
* Ability to consent
* Clinical diagnosis of BV or thrush confirmed on Gram stain
* Willing to be randomised to vaginal lactoferrin pessaries or oral antibiotics/antif…
Contacts