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Clinical Trials/NCT01315080
NCT01315080UnknownNot Applicable

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

Hospital Universitario Virgen de la Arrixaca1 site in 1 country10 target enrollmentStarted: March 2011Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Sponsor
Enrollment
10
Locations
1
Primary Endpoint
Resolution of mammillary fistula

Study Overview

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.

Study Design

Study Type
Observational
Observational Model
Case Control
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts 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

Outcomes

Primary Outcomes

Resolution of mammillary fistula

Time Frame: one year

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Hospital Universitario Virgen de la Arrixaca
Sponsor Class
Other

Study Sites (1)

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