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Clinical Trials/NCT03724903
NCT03724903CompletedNot Applicable

Ductal Lavage Versus Corticosteroids Therapy for Idiopathic Granulomatous Mastitis: a Multicenter, Randomized, Open-labelled, Non-inferior Trial.

Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University2 sites in 1 country140 target enrollmentStarted: April 1, 2019Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
140
Locations
2
Primary Endpoint
Complete Clinical Response(cCR)

Study Overview

Brief Summary

A single-arm, proof-of-concept trial has shown the safety and efficacy of ductal lavage as a treatment for idiopathic granulomatous mastitis patients (Manuscript accepted in Journal of Surgical Research 2018). In this multicenter, randomized, open-labeled, non-inferior trial, the investigators are going to enroll eligible granulomatous mastitis patients and randomized them into ductal lavage versus. corticosteroids therapy group. The primary endpoint of this study is the complete clinical response rate at 1 year after the enrollment. The aim of this study is to provide evidence for the management of idiopathic granulomatous mastitis patients .

Detailed Description

Non-lactational mastitis (NLM) consists of a broad spectrum of inflammatory breast diseases. Among them, periductal mastitis and idiopathic granulomatous mastitis(IGM) are the most commonly encountered in clinical practice. IGM can be diagnosed when all possible causes of granulomatous diseases (known mycobacterial or fungal infection, Wegener granulomatosis, sarcoidosis, etc.) are excluded. There is no consensus on the standard treatment of IGM patients. Surgery, oral corticosteroids, topical steroids, immunosuppressive therapy, and observation alone were all proposed as the treatment for IGM patients. However, all of the evidences are derived from retrospective studies. In a previous study, the investigators conducted a single-arm, proof-of-concept trial that showed the safety and efficacy of ductal lavage as a treatment for IGM patients. Ductal lavage is possible to spare the patients from corticosteroids therapy and or surgery. To further address this issue, the investigators are going to conduct this multicenter, randomized, open-labeled, non-inferior trial, to compare the efficacy and safety of ductal lavage and corticosteroids therapy. The aim of this study is to provide evidence for the management of IGM patients.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
Female
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Female, age between 18 and 65 years old.
  • •Inform consent signed.
  • •Clinical diagnosis of non-lactating mastitis, defined as mastitis occurred more than 1 month after the cessation of lactation.
  • •Clinical and pathological diagnosis of idiopathic granulomatous mastitis.
  • •Never receive surgical treatments, or corticosteroids therapy after the cessation of lactation. Core needle biopsy is allowed.
  • •Good health, judged by clinicians, to receive ductal lavage.
  • •M score >=2

Exclusion Criteria

  • •Grade III inverted nipple(Plastic. Reconstruction. Surgery. 104: 389, 1999.)
  • •Lactational mastitis patients.
  • •Bilateral IGM patients.
  • •Clinically diagnosis of periductal mastitis.
  • •Pathological diagnosis of breast carcinoma.
  • •Pregnant women.
  • •Evidences suggest possible diagnosis of SLE(systemic lupus erythematosus), rheumatic disorders or other systematic auto-immune diseases.
  • •Evidences suggest possible diagnosis of tuberculosis.
  • •Evidences suggest possible diagnosis of fungus infection of the breast
  • •History of breast trauma.
  • •History of taking oral corticosteroids or anti-tuberculosis treatment.
  • •Imaging examinations indicates foreign objects retained in the breast
  • •Presence of sepsis or severe inflammation caused by IGM, for which surgery is likely required.
  • •Patients with inappropriate coagulation function, cardiac function, pulmonary function, liver and renal function, that clinicians judges as not suitable to participate in this study.

Arms & Interventions

Corticosteroids therapy

Active Comparator

Oral corticosteroids therapy for 6 months.

Intervention: Corticosteroid therapy (Drug)

Ductal lavage

Experimental

Ductal lavage and breast massage for two weeks.

Intervention: Ductal lavage (Procedure)

Outcomes

Primary Outcomes

Complete Clinical Response(cCR)

Time Frame: 1 year since randomization

The proportion of patients that achieve M-score \<=1 at 1 year after the treatment.

Secondary Outcomes

  • Treatment failure (TF) rate(1 year since randomization)
  • Time to cCR(1 year since randomization)
  • Relapse rate(1 year since randomization)
  • Adverse events(1 year since randomization)
  • Protocol compliance rate(1 year since randomization)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Chen Kai

Dr.

Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University

Study Sites (2)

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