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Puncture Breast Abscess

Continuation of Breastfeeding After Management of Breast Abscesses by Ultrasound-guided Punctures

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03730467
Acronym
PONCTABCESEIN
Enrollment
0
Registered
2018-11-05
Start date
2018-09-04
Completion date
2018-09-04
Last updated
2026-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Abscess

Keywords

Breast feeding, breast abscess, ultrasound-guide, puncture, health

Brief summary

Several breast diseases can complicate breastfeeding : 4% of women develop a mastitis and 1% develop an abscess. The study deals with cases of breast abscess that have been treated according to a defined protocol (Parisian Perinatal Health Network), by a multidisciplinary team (center of Medical Imaging Duroc) trained in breastfeeding and ultrasound-guided punctures. The aim of the study is to define the risk factors for the onset of a breast abscess, to evaluate the indications and methods of management of abscess by ultrasound puncture, and to provide arguments motivating the continuation of breastfeeding.

Interventions

BEHAVIORALPhone call to the patient

Phone call to the patient

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER
URC-CIC Paris Descartes Necker Cochin
CollaboratorOTHER

Study design

Observational model
COHORT
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Nursing mothers * Patients referred for breast abscesses during lactation * Having an abscess confirmed ultrasoundly and indicating a puncture * Women punctured of an abscess of the breast abscess in the center of Medical Imaging Duroc * Not opposing the use of them given and to answer the questionnaire on the immediate and medium-term future by telephone * Women aged \> 18 years old * Women understanding French * Affiliated to Social Security

Exclusion criteria

No

Design outcomes

Primary

MeasureTime frameDescription
Continuation of breastfeeding1 week to 6 months after the puncturePhone call to the patient

Secondary

MeasureTime frameDescription
Etiology of the abscess1 week to 6 months after the punctureMedical record and phone call to the patient
Adequacy of medical care with the protocol of the Parisian Perinatal Health Network1 week to 6 months after the punctureMedical record and phone call to the patient
Relationship between puncture breastfeeding continuation1 week to 6 months after the punctureMedical record and phone call to the patient
Relationship between surgery and weaning1 week to 6 months after the punctureMedical record and phone call to the patient

Countries

France

Contacts

PRINCIPAL_INVESTIGATORVirginie Rigourd, MD

Assistance Publique - Hôpitaux de Paris

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 4, 2026