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.
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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

Pippa Oakeshott, MD

020 8725 0153

oakeshot@sgul.ac.uk

CONTACT

Fiona Reid, MSc

fiona.reid@kcl.ac.uk

CONTACT