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Tonsillotomy or Follow-up in PFAPA Syndrome

Tonsillotomy or Follow-up in PFAPA -Syndrome - Randomised, Controlled Study Using Sequential Design

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03331497
Enrollment
22
Registered
2017-11-06
Start date
2017-10-24
Completion date
2022-02-02
Last updated
2022-02-21

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

Conditions

PFAPA Syndrome

Brief summary

Children with periodic fever, aphthous stomatitis, pharyngitis, adenitis (PFAPA) -syndrome diagnosis will be randomised either to tonsillotomy (partial tonsillectomy) or 3 months follow up. At follow up visit 3 months after randomisation the children from either groups with ongoing symptoms will be sent to tonsillectomy.

Detailed description

Children with periodic fever, aphthous stomatitis, pharyngitis, adenitis (PFAPA) -syndrome diagnosis will be randomised either to tonsillotomy (partial tonsillectomy) or 3 months follow up. In both groups the symptoms are monitored with symptom diaries. At follow up visit 3 months after randomisation the children from either groups with ongoing symptoms will be sent to tonsillectomy (total remove of palatine tonsil). The design is sequential trial. From the previous trials we know that the effect of tonsillectomy is about 90% and that during follow up for six months as much as 50% of the patients will recover. Because the syndrome is rare and because the rescue operations of the tonsils (tonsillectomy in a person who has gone through tonsillotomy), the sample size has to be as low as possible. That is the reason why we chose sequential design, with assessments after every 8 patient. Randomization is made in blocks of four. In sequential design we use the following assumptions: * We are looking for a 40% absolute difference in cure rate between tonsillotomy (90%) and follow up (50%) groups. * Two sided Whitehead design * Maximum likelihood estimation (MLE) * Five assessments (sample size 4+4, 8+8. 12+12, 16+16 and 19+19) * type 1 error 5 % and power 80% * The sample size will be from 8 to 38 patients depending on when the trial can be stopped along assessments.

Interventions

PROCEDURETonsillotomy

About 2/3 of the palatine tonsil tissue is removed with coplator or bipolar knife.

Sponsors

Oulu University Hospital
CollaboratorOTHER
Tampere University
CollaboratorOTHER
Tampere University Hospital
CollaboratorOTHER
Turku University Hospital
CollaboratorOTHER_GOV
University of Turku
CollaboratorOTHER
University of Oulu
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
1 Years to 12 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosed PFAPA syndrome: regularly occurring fever episodes for 3-5 days for at least five times or for 6 months

Exclusion criteria

* prior tonsil surgery

Design outcomes

Primary

MeasureTime frameDescription
Cure3 months from randomizationProportion of patients who do not have any PFAPA symptoms

Secondary

MeasureTime frameDescription
Rescue surgery12 months from randomizationProportion of patients needing rescue surgery (tonsillectomy)
Days with fever3 months from randomizationNumber of days with fever \>38C in symptom diaries
Cure6 months from randomizationProportion of patients who do not have any PFAPA symptoms

Countries

Finland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026