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Pediatric Pilonidal Sinus Surgical Treatment

Comparison of Four Different Surgical Methods for the Treatment of Sacrococcygeal Pilonidal Sinus: a Randomized Controlled Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07369921
Enrollment
80
Registered
2026-01-27
Start date
2026-04-30
Completion date
2026-05-30
Last updated
2026-04-14

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

Conditions

Pediatric, Pilonidal Sinus, Surgery

Keywords

Pilonidal Sinus, pediatric surgery

Brief summary

The aim of study to evaluate four different treatment options for pilonidal sinus disease in a randomized controlled trial to find the most suitable treatment option.

Detailed description

Pilonidal sinus disease (PSD) is common in young adults and causes repeated infection and inflammation in the sacrococcygeal region. It is most common in men between the ages of 20 and 30, which is why most publications about PSD are part of adult series. This study aims to determine which treatment option is more effective and beneficial for patients with sacrococcygeal pilonidal sinus. Furthermore, it aims to contribute to more positive treatment outcomes by identifying the causes of recurrence and morbidity in patients. Sacrococcygeal pilonidal sinus is quite common in adolescents. Treatment options vary from non-operative to endoscopic surgery. However, recurrence still occurs with every technique. Patients suffer from long treatment processes and morbidity. Although the exact causes of recurrence are not fully understood, it is thought that the patient's demographic characteristics and treatment option play a role. Most studies are retrospective and compare at most two treatment options. This is one of the reasons why it is not possible to reach a definitive conclusion about which treatment is more effective. Also, the number of studies conducted in the adolescent age group is limited. By conducting study prospectively and randomized, aim to prevent biased results.

Interventions

PROCEDURECrystallized Phenol Applied

four different surgical methods for the treatment of sacrococcygeal pilonidal sinus

Sponsors

Zeliha Alicikus
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Intervention model description

randomized controlled

Eligibility

Sex/Gender
ALL
Age
12 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* having sacrococcygeal pilonidal sinus disease * written informed (family) consent were eligible for inclusion in this trial

Exclusion criteria

* Being over 18 years old or under 12 years old * recurrent sacrococcygeal pilonidal sinus disease

Design outcomes

Primary

MeasureTime frameDescription
complications30 daysRecurrence
pain score24 hoursVAS score under 4,VAS score above 4

Secondary

MeasureTime frameDescription
sinus volume measurement24 hoursUSG guided

Countries

Turkey (Türkiye)

Contacts

CONTACTZELİHA AKIŞ YILDIZ, md
zelihaakis@gmail.com+90 5305255542

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 15, 2026