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Granulomatous MastitisPhase 1/2GRANMASNCT07454772

Antibiotics vs Corticosteroids in Treatment of Granulomatous Lobular Mastitis

A Phase 1/2 study testing Steroid and Antibiotic in people with Granulomatous Mastitis, run by All India Institute of Medical Sciences, Bhubaneswar at 1 site in India.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

The goal of this clinical trial is to find the most effective and safe medical treatment for Granulomatous Lobular Mastitis (GLM) - a rare, chronic inflammatory breast disease that affects young and middle-aged women, often following childbirth. Read more about this study

Who is it for?
Any age, women only
Conditions the study is for
Granulomatous Mastitis
What is being tested?
Steroid and Antibiotic
Type of treatment
Pill or oral medicine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
72 participants
Where
1 siteIndia
Study dates
15 Mar 2026to 4 Jul 2027
Phase
Phase 1/2
Are there results?
Not yet: the study is under way

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 Any age
  • Women only
  • No healthy volunteers
  • Child, Adult, Older adult

Who may be able to join

  • Women histologically diagnosed with GLM willing to participate in the study and to come for follow up.

Who cannot join

  • Declining to participate in the study
  • Pregnant or lactating women
  • Patient already on antibiotic/steroid therapy and are responding to treatment
  • Known immunosuppression or diabetes mellitus uncontrolled
  • Patient already on immunosuppression therapy for any other disorder
  • Lost to follow-up before 3 months post-treatment
Show all 9Show fewer
  • Allergic to one of the antibiotics/steroids which will be used
  • Contraindications to oral steroids therapy
  • Contraindications to methotrexate therapy

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Maniteja Ravipati, MBBS contact

+91 7619508903

maniteja.ravipati@gmail.com

Tushar Subhadarshan Mishra, MBBS,MS contact

+91 9438884251

surg_tushar@aiimsbhubaneswar.edu.in

India1 site
  • AIIMS Bhubaneswar

    Bhubaneswar, Odisha, 751019

    Maniteja R, MS, 7619508903, maniteja.ravipati@gmail.com

Other trials in India

About this study

Official title: Antibiotics vs Corticosteroids in Treatment of Granulomatous Lobular Mastitis - A Randomized Controlled Trail

The goal of this clinical trial is to find the most effective and safe medical treatment for Granulomatous Lobular Mastitis (GLM) - a rare, chronic inflammatory breast disease that affects young and middle-aged women, often following childbirth.

The main questions it aims to answer are:

Read more

Does an antibiotic regimen (clarithromycin, ofloxacin, rifaximin) lead to faster and complete healing (Complete Clinical Response) compared to steroids?

Do steroids (prednisolone in tapering doses) provide better symptom control or cause more side effects?

Researchers will compare the antibiotic group (Group A) and the steroid group (Group B) to see which treatment results in quicker recovery, fewer side effects, and lower recurrence rates.

Participants will:

Receive a 14-day antibiotic trial initially (screening phase).

If no improvement, be randomly assigned to:

Group A (Antibiotic therapy) - Clarithromycin, Ofloxacin, Rifaximin for 8 weeks, or

Group B (Steroid therapy) - Prednisolone in tapering doses for 8 weeks.

Undergo evaluation after 2 months:

If not fully recovered, receive Methotrexate + Folic acid for another 8 weeks.

If still no improvement, switch to the alternate treatment or undergo surgery if required.

Attend regular follow-ups for 6 months for clinical assessment and monitoring of side effects.

This 2-year study aims to develop a standardized, step-by-step treatment protocol for GLM, helping improve outcomes and reduce unnecessary surgeries for affected women.

Read the detailed description

What is this study about?

This research is being done at AIIMS Bhubaneswar to find the best medical treatment for a breast condition called Granulomatous Lobular Mastitis (GLM).

GLM is a rare, long-lasting inflammation of the breast that mainly affects young and middle-aged women, often those who have recently had children. It can look very similar to breast cancer or a breast abscess, causing anxiety and sometimes unnecessary surgery.

Common symptoms include:

Painful or painless breast lump

Swelling, redness, or abscess (collection of pus)

Discharge from the nipple or retraction (nipple pulled inward)

Skin changes over the breast It can occur in one or both breasts and may come back after treatment.

Why is this study important?

At present, there is no single, standard treatment for GLM. Doctors use antibiotics, steroids, immunosuppressants (like methotrexate), or surgery - but the results vary widely. Some medicines help one patient but not another, and some cause unwanted side effects or recurrences.

This study aims to compare antibiotics and steroids directly, to identify which gives better and faster healing with fewer side effects. The goal is to develop a clear, step-by-step treatment plan for all patients with GLM.

What will happen in this study? Who can take part?

Women diagnosed with GLM by biopsy (tissue test).

Participants must be willing to attend regular follow-ups.

Women who are pregnant, breastfeeding, diabetic (uncontrolled), on other immunosuppressive treatment, or allergic to study drugs cannot participate.

How the study works:

First step (screening):

All participants will receive a short course of antibiotics for 14 days.

If the infection improves, treatment continues outside the study.

If it doesn't improve, the person will be included in the main trial.

Random assignment:

Patients will be randomly divided into two groups:

Group A - Antibiotic group: Receives clarithromycin, ofloxacin, and rifaximin tablets for 8 weeks.

Group B - Steroid group: Receives prednisolone (steroid tablets) in reducing doses for 8 weeks.

Review after 2 months:

Doctors will check whether the breast swelling and pain are gone.

If completely cured (called Complete Clinical Response or CCR), medicines are stopped.

If not cured, the patient is given an additional medicine (methotrexate + folic acid) for 8 weeks.

If still not improved:

The treatment groups are switched (antibiotic patients receive steroids, and vice versa).

If there's still no recovery, surgery (like abscess drainage or lump removal) will be considered.

Throughout the study, symptoms, side effects, and any need for surgery will be recorded carefully.

How long does participation last?

Each participant will be followed for around 6 months - this includes treatment, monitoring, and follow-up visits.

Possible benefits for participants

Regular medical check-ups, follow-ups, and investigations by specialist doctors.

Chance of receiving an effective, well-monitored treatment plan.

Early detection of complications and quick medical management.

Contribution to medical knowledge that may help future patients avoid prolonged or incorrect treatment.

Possible side effects or risks

All medicines used in this study are commonly prescribed and generally safe under supervision.

However, possible side effects may include:

For antibiotics: stomach upset, nausea, mild diarrhea, or allergy (rare).

For steroids: weight gain, bloating, mood changes, increased appetite, or joint pain.

For methotrexate: mild fatigue, nausea, or rare liver enzyme changes (monitored closely).

Doctors will monitor all participants closely and adjust or stop treatment if any problems arise.

Any abscess or fluid collection will be drained if needed, and pain will be managed with appropriate medicines.

Confidentiality and voluntary participation

All personal information will be kept strictly confidential. Participants' names will not appear in any reports or publications. Joining this study is completely voluntary. You may leave the study at any time without affecting your future medical care.

Costs and compensation

All investigations and medicines that are part of routine care are free or low-cost.

The average expected expense is about ₹2500, which includes only the patient's regular medical costs.

If any research-related injury occurs, the hospital will provide free treatment.

Expected outcomes

By comparing results between antibiotics and steroids, this study aims to:

Identify which treatment helps more women achieve complete healing faster.

Understand which drugs have fewer side effects.

Reduce the need for surgery and recurrence.

Develop a standardized treatment protocol for GLM.

If antibiotics are found to be equally effective or better, they could become the first-line, low-cost, safer option - especially in areas with limited resources.

If steroids prove superior, their dosage and duration can be refined to minimize side effects.

Study time - 2 years

Being tested
Steroid, Antibiotic
Medical subject headings
Granulomatous Mastitis

What participants receive

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

  • SteroidDrug

    Also called Tab Prednisolone, Inj Triamcinalone

    Once randomized into the steroid arm, oral therapy with Tab. Prednisolone 20mg BD will be given for 14days, Tab. Prednisolone 10mg BD will be given for 21 days, Tab. Prednisolone 5mg BD will be given for 14days and Tab. Prednisolone 2.5mg BD will be given for 7 days(tapering dose) will be used in this intervention compared to antibiotics which are used in other.

    If the rate of response to oral steroids is slow and therapy prolonged, intralesional steroids (Inj. Triamcinalone 40mg) will be given as deemed required.

  • AntibioticDrug

    Also called Tab Clarithromycin 500, Tab Ofloxacin 400

    Once randomized into the antibiotic arm, dual oral antibiotic therapy with Ofloxacin 400mg and Clarithromycin 500mg will be used in this intervention compared to steroids which are used in other

Study groups in NCT07454772
Study groupRoleWhat they receive
ARM CorticosteroidActive comparatorSteroids are used to treat GLM
Receives: Drug: Steroid
ARM AntibioticActive comparatorAntibiotics are used to treat GLM
Receives: Drug: Antibiotic

What is being measured

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

  1. Primary outcome

    To compare the efficacy of antibiotics vs corticosteroids in achieving Complete Clinical Response (CCR) via clinical and radiological assessment in GLM patients at two months of the treatment started in the adaptive randomized arm.

    CCR will be defined as no clinical signs and symptoms of the disease and no recurrence for 6 weeks.

    Measured: 2 months

Secondary outcomes (11)
  1. To assess the safety and tolerability of each treatment regimen

    To assess the safety and tolerability of each treatment regimen via clinical assessment leading to the detection of any side effects, namely weight gain, skin changes, diabetes mellitus, bone pain, menstrual irregularities, hirsuitism, cataract, glaucoma, joint pains, tendonitis, skin ulcers, and heart rhythm changes.

    Any of the above side effects, debilitating enough to warrant stoppage of therapy will define tolerability. Development of irreversible side effects will define safety of the treatment regimen.

    Measured: 2 months

  2. To assess the the proportion of patients requiring surgery in the treatment of GLM

    Determining the proportion of patients requiring surgery, based on surgical procedures performed on basis of clinical examination findings suggestive of abscess.

    Aspiration and minisuction drain(6 french aspiration catheter/pigtail) will be not be considered as a surgical procedure

    Measured: 2 months

  3. To assess the role of different quantum of surgery needed (Incision and Drainage/Resection/mastectomy) in the treatment of GLM

    Determining the Quantum of surgery needed (Incision and Drainage/Resection/mastectomy), based on surgical procedures performed on basis of clinical examination findings suggestive of abscess.

    Aspiration and minisuction drain(6 french aspiration catheter/pigtail) will be not be considered as a surgical procedure

    Measured: 2 months

  4. To assess the number of patients have recurrence after surgery in the treatment of GLM

    Determining the number of patients have recurrence after surgery performed in the institution or outside, based on surgical procedures performed on basis of clinical examination findings suggestive of abscess.

    Aspiration and minisuction drain(6 french aspiration catheter/pigtail) will be not be considered as a surgical procedure

    Measured: 2 months

  5. To assess the number of patients requiring Aspiration/ minisuction drain(6 french aspiration catheter/pigtail) in the treatment of GLM

    Determining the number of patients requiring Aspiration/ minisuction drain(6 french aspiration catheter/pigtail) on basis of clinical examination findings suggestive of abscess.

    Measured: 2 months

  6. To assess the failure rate of aspiration/ minisuction drain(6 french aspiration catheter/pigtail) in the treatment of GLM

    Determining the proportion of aspiration/minisuction drain failures from procedures performed on basis of clinical examination findings suggestive of abscess.

    Measured: 2 months

  7. To determine the Indications of immunosuppressive therapy in the treatment of GLM

    To determine the indications of immunosuppressive therapy (failure to achieve CCR within 2 months/Relapse/cure, side effects of primary medications), started after non response to intervention arm drugs

    Measured: 2 months

  8. To To determine the proportion of patient requiring combination immunosuppressive therapy in the treatment of GLM

    To determine the proportion of patient requiring combination immunosuppressive therapy started after non response to intervention arm drugs

    Measured: 2 months

  9. To determine the average duration of immunosuppressive therapy required in the treatment of GLM

    Average duration of immunosuppressive therapy required, started after non response to intervention arm drugs

    Measured: 2 months

  10. Histological pattern (neutrophilic/lymphocytic/mixed)

    To compare the proportion of patients with each of the histological variety (neutrophilic/lymphocytic/mixed) of GLM attaining complete response to therapy in each arm.

    Measured: 2 months

  11. Proportion of CCR obtained in each histological pattern (neutrophilic/lymphocytic)

    To assess the proportion of CCR obtained in each histological pattern (neutrophilic/lymphocytic).

    Measured: 2 months

Timeline

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

  1. First posted6 Mar 2026
  2. Study start15 Mar 2026 (estimated)
  3. Primary completion4 Apr 2027 (estimated)
  4. Study completion4 Jul 2027 (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 1/2
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Crossover
Masking
None (open label)
Enrolment
72 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07454772
Sponsor's protocol ID
ECR/534/inst/OD/2014/RR-25
Acronym
GRANMAS
Status last verified
Feb 2026
First submitted
17 Nov 2025
Last updated
6 Mar 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A Phase 1/2 study testing Steroid and Antibiotic in people with Granulomatous Mastitis, run by All India Institute of Medical Sciences, Bhubaneswar at 1 site in India.

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 9 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: opening soon, as of the sponsor's last update on 6 Mar 2026. 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 India. 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 combined phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

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

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

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

Contact Maniteja Ravipati, MBBS (+91 7619508903, maniteja.ravipati@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Primary outcome (time frame: 2 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 Mar 2026.

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