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Comparison of the two treatment modalities (crystallized phenol application vs. surgical treatment) for pilonidal sinus disease

Comparison of crystallized phenol application and surgery on quality of life and pain in patients for pilonidal sinus disease

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12612000868886
Enrollment
150
Registered
2012-08-16
Start date
2012-06-15
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

Pilonidal sinus disease is an acquired disease at the sacrococcygeal region that can be treated by a number of surgical techniques. Crystallized phenol application seems to be an alternative therapy for pilonidal sinus disease with higher success rates, lower costs, faster recovery and earlier return to work. The aim of this presentation is to compare the crystallized phenol application and surgery for pilonidal sinus disease .

Interventions

Patients were randomized to 2 groups according to applied treatment protocol Group 1: Crystallized phenol will be applied into pilonidal sinus tract. The amount of the crystallized phenol will differ according to the patients sinus tract. the patient will be followed for three weeks for wound healing. Closure of the sinus tract in three weeks will be accepted as cure. In case of failure in the healing of sinus tract in three weeks, the crystallized phenol application will be performed respectiv

Patients were randomized to 2 groups according to applied treatment protocol Group 1: Crystallized phenol will be applied into pilonidal sinus tract. The amount of the crystallized phenol will differ according to the patients sinus tract. the patient will be followed for three weeks for wound healing. Closure of the sinus tract in three weeks will be accepted as cure. In case of failure in the healing of sinus tract in three weeks, the crystallized phenol application will be performed respectively. Group 2: Surgical technique either primary closure or marsupialization will be performed. primary closure for patients who does not have infection on the surgical site and marsupialization for patients who had acute infection on surgical site were the reason for surgery technique . For both techniques the duration of surgery were estimated as 1 hour. The patients follow up will continue until the full wound healing occurs.

Sponsors

Kamil Gulpinar
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
0 to No maximum
Healthy volunteers
No

Inclusion criteria

patients with pilonidal sinus disease

Exclusion criteria

patients with acute abcess

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 11, 2026