Evaluation of Quality of Life After Facial Hyaluroic Acid Injections Following Treatment for Breast Cancer.
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Inject of hyaluronic acid in the face.
- Who it may be relevant to
- Registry conditions: Breast Cancer, Aesthetic Improvement of the Skin. Basic parameters: 18 years — 50 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
Breast cancer, the most common cancer in women, is increasingly managed as a chronic disease thanks to therapeutic advances. However, treatments such as chemotherapy and hormonotherapy often induce premature menopause in younger women, leading to skin aging, atrophy, and distressing symptoms that negatively affect quality of life. These cutaneous effects are frequently overlooked despite their psychological and social impact. Hyaluronic acid injections, already well established in aesthetic and reconstructive medicine, may offer a safe, minimally invasive option to restore skin quality, improve self-esteem, and enhance overall well-being in breast cancer survivors. This study aims to assess their efficacy and safety in this specific population.
Interventions
- Device Inject of hyaluronic acid in the face
The patient may receive up to 1 ml (volume of one syringe) of each of the three HA references (between 1 ml and 3 ml maximum). The HA reference(s) to be injected will be chosen on the basis of the investigator's assessment and the patient's desired correction.
Primary outcome measures
- Facial appearance following facial hyaluronic acid injection following breast cancer treatment. [Time frame: 3 months]
- Health-related quality of life followig facial hyaluronic acid injection following breast cancer treatment. [Time frame: 3 months]
- Adverse effects following facial hyaluronic acid injection following breast cancer treatment. [Time frame: 3 months]
Eligibility criteria
Inclusion criteria
- Women ≥ 18 years old and ≤ 50 years old.
- Non-menopausal status at time of diagnosis of breast cancer (self-reporting).
- Patient with breast cancer (uni or bilateral):
- treated at the Institut Bergonié by chemotherapy (+/- targeted/immunotherapy) and surgical treatment (conservative or not) and/or hormone therapy and/or radiotherapy
- who completed their treatment at least 6 months ago including end of treatment with Herceptin but with the exception for ongoing hormone therapy
- in complete remission
- Non-immunosuppressed patient.
- Voluntarily signed and dated written informed consent prior to any study specific procedure.
- Patient affiliated to a social security in compliance with Article 1121-11 of the French Public Health Code.
Exclusion criteria
- Patients with a history of or declared autoimmune disease or immune system deficiency or undergoing immunosuppressive treatment. A 6-month washout is required.
- Patients undergoing or planning to undergo peeling treatment or laser/ultrasound-based or botox treatment or hyaluronic acid injections during the study or having had one of these treatments in the 6 months preceding the study.
- Patients showing cutaneous disorders, inflammation or infection (acne, herpes labialis, scars…) at the treatment site or near to this site.
- Patients having a known hypersensibility to lidocaine and/or amide local anaesthetic agents or hyaluronic acid and/or proteins from gram-positive bacteria, or with a history of severe allergy or anaphylactic shock.
- Patients with a history of streptococcal disease (recurrent sore throat, rheumatic fever)
- Patients with autoimmune or cardiac diseases (i.e. heart conduction disorders) and/or undergoing treatment for heart diseases (beta-blockers).
- Patients with hepatocellular insufficiency and/or undergoing treatment for liver disease.
- Patients suffering from epilepsy not controlled by a treatment or porphyria.
- Patients with a tendency to develop hypertrophic scars.
- Patients with severe, ongoing and/or uncontrolled disease that may pose a health risk to the patient during the study and/or may have an impact on the study assessments.
- Patients receiving or planning to receive high dose Vitamin E, aspirin, anti-inflammatories, or anti-coagulant during the week preceding each injection
- Patients receiving any long-term medical treatment or any treatment that, in the opinion of the clinical investigator, may interfere with test results or put the patient at undue risk.
- Patients under guardianship/tutorship.
- Pregnant women or breastfeeding mothers.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Supportive care
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07425548 · IB 2025-01