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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COMPLETED
419 participants
OBSERVATIONAL
2016-04-08
2017-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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ambulatory surgery description
Medical questionnaire
* quality of life questionnaire (EORTC QLQ-C30 and QLQ-BR23)
* Hospital Anxiety and Depression scale
* satisfaction care questionnaire (IN-PATSAT32)
Interventions
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Medical questionnaire
* quality of life questionnaire (EORTC QLQ-C30 and QLQ-BR23)
* Hospital Anxiety and Depression scale
* satisfaction care questionnaire (IN-PATSAT32)
Eligibility Criteria
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Inclusion Criteria
* age \>18 years old
* understand and comply with the requirements of the study
* patient must be affiliated to a social security system
Exclusion Criteria
* bilateral breast surgery
* patient already included in another clinical trial with an experimental molecule
* men
* patient deprived of liberty or under supervision
* neoadjuvant therapy
18 Years
FEMALE
No
Sponsors
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Institut de Cancérologie de Lorraine
OTHER
Responsible Party
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Principal Investigators
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MARCHAL FREDERIC, MD, PU-PH
Role: PRINCIPAL_INVESTIGATOR
Institut de Cancérologie de Lorraine
Locations
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Institut de Cancérologie de Lorraine
Vandœuvre-lès-Nancy, , France
Countries
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References
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Hejl L, Raft J, Leufflen L, Rauch P, Buhler J, Abel-Decollogne F, Routiot T, Hotton J, Salleron J, Marchal F. Quality of life, anxiety, and postoperative complications of patients undergoing breast cancer surgery as ambulatory surgery compared to non-ambulatory surgery: A prospective non-randomized study. J Gynecol Obstet Hum Reprod. 2021 Feb;50(2):101779. doi: 10.1016/j.jogoh.2020.101779. Epub 2020 May 11.
Other Identifiers
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ICL OBS 01
Identifier Type: -
Identifier Source: org_study_id
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