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Treatment Alternatives for acute Sore Throat in Everyday practice

A primary care randomised controlled trial of probiotics, xylitol and sorbitol for acute sore throat

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN51472596
Enrollment
401
Registered
2010-04-29
Start date
2008-11-01
Completion date
Unknown
Last updated
2018-03-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Topic: Primary Care Research Network for England

Interventions

Patients will be approached by either advertising in the practice, when seeing their doctor/nurse (who will provide information to the patient with the consent form) or by writing to patients with kno

Sponsors

University of Southampton (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Presenting with acute sore throat 2. Over the age of 16 years, either sex

Exclusion criteria

Exclusion criteria: 1. History suggestive of quinsy 2. Previous rheumatic fever, glomerulonephritis 3. Phenylketonuria 4. Allergy to xylitol, sorbitol or probiotics 5. Patients unwilling or unable to self medicate with gum or probiotics for the duration of the study or complete outcome measures 6. Subjects with serious chronic disorders where antibiotics are automatically needed (e.g. cystic fibrosis) 7. Suspected pregnancy 8. Immune deficiency

Design outcomes

Primary

MeasureTime frame
The mean score for sore throat and difficulty swallowing during 2 - 5 days after presentation

Secondary

MeasureTime frame
1. Time to resolution of sore throat 2. Time taken off work or unable to do normal activities 3. Satisfaction with treatment

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 25, 2026