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An evaluation of the self-use of bulb syringes for the self-treatment of ear wax and their impact on primary care workload - a randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN71172551
Enrollment
236
Registered
2005-09-29
Start date
2004-02-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Ear wax Ear, Nose and Throat Ear wax

Interventions

Self-treatment using a bulb syringe compared with the standard treatment of syringing by a practice nurse or GP.

Sponsors

University of Southampton (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Adults presenting at participating surgeries with symptoms of ear wax and having wax occluding one or both ear drums.

Exclusion criteria

Exclusion criteria: History of perforated ear drum, other significant ear disease or surgery, signs of perforation or infection in the affected ear, patients with cognitive impairment sufficient to preclude them from following the instructions or completing the questionnaire.

Design outcomes

Primary

MeasureTime frame
1. Objective clearance of wax 2. Relief of symptoms 3. Acceptability of treatment 4. Unwanted effects of treatment 5. Proportion of people requiring further intervention within 6 weeks 6. Costs of prescriptions for subsequent ear care in 6 weeks from randomisation

Secondary

MeasureTime frame
Rates of consultation with GP and practice nurse for ear care at one and two years.

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026