Use of Probiotic Lactobacilli for the Treatment of Lactational Mastitis
This study has been completed.
Sponsor:
Universidad Complutense de Madrid
Information provided by:
Universidad Complutense de Madrid
ClinicalTrials.gov Identifier:
NCT00716183
First received: July 14, 2008
Last updated: May 22, 2009
Last verified: May 2009
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Purpose
A total of 300 women with lactational infectious mastitis will daily ingest 9 log10 cfu of Lactobacillus salivarius HN6, Lactobacillus reuteri CR20 or Lactobacillus fermentum LC40 for 4 weeks. The three lactobacilli strains were originally isolated from milk of healthy women. On days 0 and 28, milk samples will be collected, and staphylococci/streptococci and lactobacilli will be counted and identified. Evolution of clinical signs will be recorded by midwifes on days 0, 7, 14 and 28.
| Condition | Intervention | Phase |
|---|---|---|
| Mastitis | Biological: Lactobacillus salivarius HN6 Biological: Lactobacillus reuteri CR20 Biological: Lactobacillus fermentum LC40 Drug: Beta-lactam antibiotic | Phase 2 Phase 3 |
| Study Type: | Interventional |
| Study Design: | Allocation: Non-Randomized Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Phase 2/3 Evaluation of Three Lactobacilli Strains Isolated From Human Milk for the Treatment of Infectious Mastitis During the Lactation Period |
Resource links provided by NLM:
MedlinePlus related topics:
Breast Diseases
Drug Information available for:
Lactobacillus
U.S. FDA Resources
Further study details as provided by Universidad Complutense de Madrid:
Primary Outcome Measures:
- Staphylococcal and/or streptococcal count in milk [ Time Frame: 0 and 28 days ]
Secondary Outcome Measures:
- Assessment of local and systemic symptoms associated to mastitis [ Time Frame: days 0, 7, 14 and 28 ]
| Enrollment: | 300 |
| Study Start Date: | July 2008 |
| Study Completion Date: | May 2009 |
| Primary Completion Date: | July 2008 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: Probiotic 1
Women receiving Lactobacillus salivarius HN6
|
Biological: Lactobacillus salivarius HN6
9 log colony-forming units, capsules, daily, four weeks
|
|
Experimental: Probiotic 2
Women receiving Lactobacillus reuteri CR20
|
Biological: Lactobacillus reuteri CR20
9 log colony-forming units, capsules, daily, four weeks
|
|
Experimental: Probiotic 3
Women receiving Lactobacillus fermentum LC40
|
Biological: Lactobacillus fermentum LC40
9 log colony-forming units, capsules, daily, four weeks
|
|
Active Comparator: beta-lactam
The evolution of the women ascribed to the other three arms will be compared with that of 100 women suffering lactational mastitis that will follow a conventional antibiotic treatment as prescribed by the pediatrician/gynecologist
|
Drug: Beta-lactam antibiotic
Use of amoxicillin, cloxacillin or amoxicillin/clavulanic acid(500-750 mg), orally, every 8-12 h, for 2-3 weeks (as prescribed by the physician responsible for the clinical diagnosis of lactational mastitis)
Other Name: Amoxicillin (generic), Cloxacillin (generic), Amoxicillin/clavulanic acid (generic), Clamoxyl, Orbenin, Augmentine
|
Eligibility| Ages Eligible for Study: | 19 Years to 38 Years (Adult) |
| Sexes Eligible for Study: | Female |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Clinical diagnosis of mastitis
- Staphylococcal and/or streptococcal count higher than 3000 colony-forming units per ml of milk
- Milk leukocyte count higher 6 log10/mL
- Must be able to provide a milk sample without the aid of a milk pump
Exclusion Criteria:
- Mammary abscesses
- Any kind of parallel disease
Contacts and Locations
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For general information, see Learn About Clinical Studies.
Please refer to this study by its ClinicalTrials.gov identifier: NCT00716183
Please refer to this study by its ClinicalTrials.gov identifier: NCT00716183
Locations
| Spain | |
| Dpt. Nutricion, Bromatologia y Tecnologia de los Alimentos | |
| Madrid, Spain, 28040 | |
Sponsors and Collaborators
Universidad Complutense de Madrid
More Information
Publications:
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Juan M. Rodríguez, Universidad Complutense de Madrid |
| ClinicalTrials.gov Identifier: | NCT00716183 History of Changes |
| Other Study ID Numbers: |
Promast08 |
| Study First Received: | July 14, 2008 |
| Last Updated: | May 22, 2009 |
Keywords provided by Universidad Complutense de Madrid:
|
mastitis Staphylococcus Streptococcus lactation breastfeeding |
Additional relevant MeSH terms:
|
Mastitis Puerperal Disorders Pregnancy Complications Breast Diseases Skin Diseases Anti-Bacterial Agents Amoxicillin Clavulanic Acids Clavulanic Acid |
Lactams beta-Lactams Cloxacillin Antibiotics, Antitubercular Anti-Infective Agents Antitubercular Agents Enzyme Inhibitors Molecular Mechanisms of Pharmacological Action beta-Lactamase Inhibitors |
ClinicalTrials.gov processed this record on July 17, 2017


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