Trials / Not Yet Recruiting
Not Yet RecruitingNCT07512648
Efficacy and Safety of Sanyong Jiedu Granules in Treating Lumps-Type Non-Lactational Mastiti
Efficacy and Safety of Sanyong Jiedu Granules in Treating Lumps-Type Non-Lactational Mastitis: A Prospective Multicentre Randomised Controlled Trial
- Status
- Not Yet Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 210 (estimated)
- Sponsor
- Caigang Liu · Academic / Other
- Sex
- Female
- Age
- 20 Years – 50 Years
- Healthy volunteers
- Not accepted
Summary
To evaluate the efficacy and safety of Sanyong Jiedu Granules in treating non-lactational mastitis with lump formation, and to investigate the relationship between its clinical efficacy and treatment duration.
Detailed description
This study is a randomised controlled trial comprising three phases: the screening phase, the treatment phase and the follow-up phase. 1. Screening phase: A total of 210 patients with mastitis who were not breastfeeding and met the inclusion and exclusion criteria were enrolled in either the experimental group or the control group, with 70 patients in each of Experimental Group 1, Experimental Group 2 and the control group. 2. Treatment phase: Experimental Group 1: San Yong Jie Du Granules group: San Yong Jie Du Granules were taken with boiled water, 10 g per dose, three times daily, for 56 consecutive days or until symptoms were completely resolved or stabilised; Experimental Group 2: San Yong Jie Du Granules + guideline-based medication group: Treatment regimen for plasma cell mastitis: Patients without cephalosporin allergy: Oral cefuroxime axetil tablets (brand name: Dalixin®), 250 mg twice daily + oral metronidazole tablets, 0.4 g three times daily, for 7-10 consecutive days; In addition, take San Yong Jie Du Granules, 10g three times daily, for 56 consecutive days or until symptoms have completely resolved or stabilised; For patients allergic to cephalosporins: Oral levofloxacin tablets, 0.5g once daily + oral metronidazole tablets, 0.4g three times daily, for 7-14 consecutive days; In addition, take San Yong Jie Du Granules three times daily, 10g per dose, for 5-6 days or until symptoms have completely resolved or stabilised; Treatment regimen for granulomatous lobular mastitis: Take oral methylprednisolone tablets (brand name: Metrol®), 20 mg once daily, for 14 consecutive days. Once symptoms have subsided, gradually reduce the dose every 1-2 weeks to 16, 12, 8, and 4 mg/day; In addition, take San Yong Jie Du Granules, 10 g three times daily, for 56 consecutive days or until symptoms have completely resolved or stabilised; Control group: Standard guideline treatment group, i.e. treatment is based on the 2016 'Expert Consensus on the Diagnosis and Treatment of Non-lactational Mastitis' issued by the Breast Health and Breast Disease Prevention and Control Working Group of the Women's Health Branch of the Chinese Preventive Medicine Association. The two main types of non-lactational mastitis-plasma cell mastitis and granulomatous lobular mastitis-are treated in accordance with the expert consensus respectively. Treatment regimen for plasma cell mastitis: For patients without cephalosporin allergy: oral cefuroxime axetil tablets (brand name: Dalixin®), 250 mg twice daily, plus oral metronidazole tablets, 0.4 g three times daily, for 7-10 consecutive days. For patients allergic to cephalosporins: oral levofloxacin tablets, 0.5 g once daily, plus oral metronidazole tablets, 0.4 g three times daily, for 7-14 consecutive days. Treatment regimen for granulomatous lobular mastitis: Oral methylprednisolone tablets (brand name: Metrol®), 20 mg once daily for 14 consecutive days; following symptom relief, the dose should be gradually reduced every 1-2 weeks to 16, 12, 8, and 4 mg/day, and continued for 56 days or until symptoms are completely resolved or stabilised. Prior to the completion of the primary efficacy endpoint assessment (i.e. before week 8 of treatment), no destructive surgical procedures aimed at lesion clearance are permitted in any group, except in cases meeting the criteria for initiation of salvage therapy. 3. Follow-up points and time windows: 2 weeks (±1 day) after commencement of medication, 4 weeks (±2 days) after commencement of medication, and upon completion of treatment/discontinuation of medication (±4 days). 4. Follow-up period: Follow-up points and time windows: 4 weeks (±7 days) after discontinuation of treatment, 3 months (±7 days) after discontinuation of treatment.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Sanyong Jiedu Granules | Prescribe Sanyong Jiedu Granules, to be taken with hot water, 10 g per dose, three times daily, for a course of 56 days or until symptoms have completely resolved or stabilised. |
| DRUG | Standard Medication | Treatment regimen for plasma cell mastitis: For patients without cephalosporin allergy: oral cefuroxime axetil tablets (brand name: Dalixin®), 250 mg twice daily, plus oral metronidazole tablets, 0.4 g three times daily, for 7-10 consecutive days. For patients allergic to cephalosporins: oral levofloxacin tablets, 0.5 g once daily, plus oral metronidazole tablets, 0.4 g three times daily, for 7-14 consecutive days. Treatment regimen for granulomatous lobular mastitis: Oral methylprednisolone tablets (brand name: Metrol®), 20 mg once daily for 14 consecutive days; following symptom relief, the dose should be gradually reduced every 1-2 weeks to 16, 12, 8, and 4 mg/day, and continued for 56 days or until symptoms are completely resolved or stabilised. |
Timeline
- Start date
- 2026-03-20
- Primary completion
- 2028-04-29
- Completion
- 2028-07-31
- First posted
- 2026-04-06
- Last updated
- 2026-04-06
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT07512648. Inclusion in this directory is not an endorsement.