Complications After Lumpectomy, Sentinel Node and Radiotherapy in Breast Cancer Patients and Physiotherapy Care
NCT ID: NCT04444882
Last Updated: 2022-08-09
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
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
71 participants
OBSERVATIONAL
2021-06-01
2022-01-28
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
The investigators expect to see a lack of consultation of physiotherapists by patients despite a significant number of complications, impacting the quality of life.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Local and Regional Radiotherapy for Nipple Sparing Mastectomy With Implant
NCT05213962
Sentinel Node Biopsy in Breast Cancner: Omission of Axillary Clearance After Micrometastasis
NCT02049632
Mastectomy in Ambulatory Breast Surgery
NCT03003169
Multidisciplinary Rehabilitation Programme for Breast Cancer
NCT05306808
Radiotherapy After Mastectomy for Breast Cancer Patients at Increased Risk of Local Recurrence
NCT03101683
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_ONLY
CROSS_SECTIONAL
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Patients with a good command of French in order to understand the letter of information and the questionnaire.
* Patients treated at the "Couple Enfant Hospital" in Grenoble. We have chosen to take patients who have been operated on at least 3 months ago (average time of end of radiotherapy).
Exclusion Criteria
* Patient with difficulties understanding, expressing or reading the French language
* Vulnerable patient or patient with impaired cognitive capacities (dementia, confusion)
* Patient subject to a legal protection measure or out of state to express her opposition (guardianship, curatorship)
FEMALE
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University Hospital, Grenoble
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Caroline Bordin-Goffin
Role: STUDY_DIRECTOR
IFMK Saint Martin d'Hères
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Chu Grenoble Alpes
Grenoble, , France
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2020-A00966-33
Identifier Type: OTHER
Identifier Source: secondary_id
38RC20.120
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.