Local Treatment of Breast Pain Based on the Daily Use of a Topical Gel
NCT ID: NCT07257770
Last Updated: 2025-12-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
50 participants
INTERVENTIONAL
2025-09-11
2026-04-11
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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treatment inositol
daily administration of the gel
inositol
Topical application of a medical device based on inositol
Control
No treatment, clinical follow up
No interventions assigned to this group
Interventions
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inositol
Topical application of a medical device based on inositol
Eligibility Criteria
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Inclusion Criteria
* Women who underwent breast surgery at least 15 days prior
* Women experiencing breast pain associated with the surgical wound
Exclusion Criteria
* Ongoing systemic and/or local pain therapy
* Pregnant women
18 Years
70 Years
FEMALE
No
Sponsors
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Lo.Li.Pharma s.r.l
INDUSTRY
Responsible Party
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Locations
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Policlinico Umberto I
Roma, , Italy
Countries
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Central Contacts
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Other Identifiers
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INO-BREAST
Identifier Type: -
Identifier Source: org_study_id
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