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Granulomatous MastitisPhase 4MSTIGMNCT02959580

Medical and Surgical Treatment for Idiopathic Granulomatous Mastitis

A Phase 4 study testing Hydrocortisone Butyrate and extended excision in people with Granulomatous Mastitis, run by Peking Union Medical College Hospital at 1 site in China.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

This study evaluates the clinical response rate of topical steroids in the treatment of idiopathic granulomatous mastitis in female adults. Half of the participants will receive topical steroid and the other half will receive local wide surgical excision. Read more about this study

Who is it for?
Ages 18 to 60 years, women only
Conditions the study is for
Granulomatous Mastitis
What is being tested?
Hydrocortisone Butyrate and extended excision
Type of treatment
Surgery or procedure
Could I receive a placebo?
No, everyone receives an active treatment
How many people
100 participants
Where
1 siteChina
Study dates
1 Jan 2017to Sep 2020
Phase
Phase 4
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 60 years
  • Women only
  • No healthy volunteers
  • Adult

Who may be able to join

  • Idiopathic Granulomatous Mastitis

Who cannot join

  • Breast Carcinoma

Trial locations and contacts

1 site in 1 country.

Yanna Zhang, M.D. contact

86-10-69158703

pumchzyn@sohu.com

China1 site, 1 recruiting
  • Department of Breast Surgery,Peking Union Medical College Hospital

    Beijing, Beijing Municipality, 100730

    Qiang Sun, Master, 86-010-69158720, sunqiangpumc@sina.com

    Yanna Zhang, Doctor, 86-010-69158703, pumchzyn@sohu.com

    Recruiting

Other trials in China

About this study

Official title: Evaluation of Topical Steroids and Surgical Treatment for Idiopathic Granulomatous Mastitis

This study evaluates the clinical response rate of topical steroids in the treatment of idiopathic granulomatous mastitis in female adults. Half of the participants will receive topical steroid and the other half will receive local wide surgical excision.

Read the detailed description

Idiopathic granulomatous mastitis (IGM) is a rare benign inflammatory breast disease of unknown etiology.It may present with many findings that clinically and radiologically mimic breast cancer.

Although IGM as a disease has been known for nearly four decades, the optimal treatment approach has not been established. Surgical intervention in the form of wide surgical excision was the mainstay of treatment before 1980, and is still performed depending on local expertise and preference.

Currently,surgical treatment and systemic steroid treatment are frequently employed. With the consideration of side effects of longterm systemic (oral) steroid usage, topical steroid without systemic use were assessed and showed satisfactory curative effect. But the data concerning the use of topical steroid therapy are still very limited.

Being tested
Hydrocortisone Butyrate, extended excision
Keywords
Granulomatous, Mastitis, topical steroids
Medical subject headings
Granulomatous Mastitis, Mastitis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Hydrocortisone ButyrateDrug

    topical use

  • extended excisionProcedure or surgery

    Lesion extended excision with or without a random breast dermo-glandular flap (BDGF).

Study groups in NCT02959580
Study groupRoleWhat they receive
medicalExperimentalHydrocortisone butyrate cream(0.1%) was applied to the breast by the patient twice a day on alternate days until the termination of treatment.
Receives: Drug: Hydrocortisone Butyrate
surgicalActive comparatorlesion extended excision
Receives: Procedure: extended excision

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. clinical response rate

    The clinical response is categorized into ''completely healed,'' ''inadequately healed,'' ''stable,'' ''worsened,'' or ''relapsed'' if the lesions had once healed but symptoms returned.

    Measured: six months

Secondary outcomes (1)
  1. granulomatous mastitis recurrence

    Measured: two years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted9 Nov 2016 (estimated)
  2. Study start1 Jan 2017
  3. Primary completion1 Sep 2020 (estimated)
  4. Study completionSep 2020 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
100 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02959580
Sponsor's protocol ID
PUMCH-breast-mastitis
Acronym
MSTIGM
Status last verified
Dec 2018
First submitted
7 Nov 2016
Last updated
6 Dec 2018
Results posted
No
Data monitoring committee
No
Individual data sharing
No

Publications

  • Altintoprak F, Kivilcim T, Yalkin O, Uzunoglu Y, Kahyaoglu Z, Dilek ON. Topical Steroids Are Effective in the Treatment of Idiopathic Granulomatous Mastitis. World J Surg. 2015 Nov;39(11):2718-23. doi: 10.1007/s00268-015-3147-9.

    PubMed 26148520
  • Sheybani F, Naderi HR, Gharib M, Sarvghad M, Mirfeizi Z. Idiopathic granulomatous mastitis: Long-discussed but yet-to-be-known. Autoimmunity. 2016 Jun;49(4):236-9. doi: 10.3109/08916934.2016.1138221. Epub 2016 Feb 1.

    PubMed 26829298
  • Benson JR, Dumitru D. Idiopathic granulomatous mastitis: presentation, investigation and management. Future Oncol. 2016 Jun;12(11):1381-94. doi: 10.2217/fon-2015-0038. Epub 2016 Apr 12.

    PubMed 27067146

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Hydrocortisone Butyrate and extended excision in people with Granulomatous Mastitis, run by Peking Union Medical College Hospital at 1 site in China.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 6 Dec 2018. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in China. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

Contact Yanna Zhang, M.D. (86-10-69158703, pumchzyn@sohu.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

clinical response rate (time frame: six months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02959580, which also lists 3 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 Dec 2018.

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