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Efficacy of Percutaneous Injection of Triamcinolone in the Treatment of Mammillary Fistula

Efficacy of Percutaneous Injection of Triamcinolone in the Treatment of Mammillary Fistula

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01315080
Enrollment
10
Registered
2011-03-15
Start date
2011-03-31
Completion date
2012-09-30
Last updated
2011-03-15

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

Conditions

Mammillary Fistula

Keywords

mammillary fistula, triamcinolone, ultrasound management, percutaneous treatment

Brief summary

The investigators recently proposed a new hypothesis on the pathogenesis of mammillary fistulae (MF) suggesting that occlusion of hair follicles by keratinous plugging may relevantly contribute to the development of MF. The investigators believe that the pathogenesis of MF mimics the behaviour of hidradenitis suppurative, as both clinical entities manifest themselves as a chronic, suppurative and recurrent inflammatory process. This new proposal has led to the present suggestion of a therapeutic alternative for MF.

Detailed description

To compare the results from a prospective observational database with two groups of patients: 1. patients with MF treated by percutaneous drainage and saline solution. 2. patients with MF treated by percutaneous drainage and saline solution plus percutaneous triamcinolone. These patients are treated following usual clinical practice in our Department. All the procedures are made through an ultrasound-guided way. During the follow-up of these cases (clinical and with ultrasound) resolution rate will be registered by the same investigator. The follow-up will be at least 6 months.

Interventions

None listed

Sponsors

Hospital Universitario Virgen de la Arrixaca
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* mammillary fistula * older than 18 years * patient acceptation to the recruitment

Exclusion criteria

* diabetes mellitus * arterial hypertension * immunodepression * peptic ulcer * chronic bowel inflammatory diseases

Design outcomes

Primary

MeasureTime frame
Resolution of mammillary fistulaone year

Countries

Spain

Contacts

Primary ContactJuan D Berna, MD PhD
jdberna@um.es+34 968369500

Outcome results

None listed

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