Covid19
Conditions
Brief summary
The major impact of COVID-19 has been that the severity of respiratory symptoms require intensive hospital treatment. There is significant mortality and many of the survivors have a delayed recovery requiring intensive prolonged rehabilitation. COVID-19 is a multi-systemic disease in which different mechanisms within the body are affected; including the 'Gut microbiome'. 'Gut microbiome' refers to the bacteria living in intestines. While some bacteria is harmful, many are extremely beneficial and necessary for a healthy body. Many patients have gastrointestinal symptoms and there is a major change in the gut micro flora (microbiome), which may have an adverse effect on the respiratory symptoms. The probiotic, Sivomix, was given to hospitalized COVID-19 patients was associated with a more rapid recovery in gastrointestinal symptoms on day 3 and 7, and an eight fold reduction in the requirement for mechanical ventilation in an open trial. This is a randomized clinical trial, with a recruitment target of 60 patients admitted with COVID-19 symptoms to the general medical wards. Patients will be randomized to receive the probiotic, Symprove, or placebo in addition to their standard of care treatment. Patients will need take either probiotic/placebo daily for 3 months. All follow-up will be whilst they are an inpatient or as a telephone follow-up; they will not need to attend at the hospital to participate. There is a biological sub-study incorporated into the protocol, but participation is optional. If patients consent to this, they will also need to provide blood, faecal and saliva samples at baseline, Day 7 and final visit (3 months after randomisation). Patients who consent to providing biological samples will need to visit the hospital at Day 7 and final visit.
Interventions
OTHERSymprove (probiotic)
Symprove's unique water-based formula is packed full of live, active bacteria. It is a probiotic, not a drug.
OTHERPlacebo
Matched placebo to Symprove probiotic
Sponsors
King's College Hospital NHS Trust
Study design
Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No
Inclusion criteria
* Symptomatic patients who are hospitalised with respiratory COVID-19 * Ability to give informed consent * Aged 20-85
Exclusion criteria
* Patients not meeting the inclusion criteria that have COVID-19 * Inability to consent * Pregnancy * Severe pre-existing mental health disorders or addictions
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Length of hospital stay | 12 months | To assess if taking the probiotic Symprove reduces the length of hospital stay of patients with symptomatic respiratory COVID-19 infection |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Clinical symptoms | 7 days | Whether administration of Symprove is associated with significantly greater improvements in clinical symptoms as opposed to placebo on day 3 and 7. |
| Intestinal inflammation | 3 months | Whether Symprove reduced intestinal inflammation as compared with that seen in placebo are improved (at day 7 and 3 months). |
| Symptom recovery | 3 months | Whether symptom recovery is more complete with the probiotic 3 months from the onset of the trial (all subjects will receive Symprove or placebo for 3 months). |
Countries
United Kingdom
Contacts
Primary ContactBu'Hussain Hayee, BSc, MBBS, FRCP, PhD
Backup ContactRefah Z Ahmed, BA MSc
Outcome results
None listed