BridgeMD
New treatment option for Breast Cancer Surgery
Official title Improvement in Breast Skin Sensibility After Breast Reconstruction: a Comparison of 3 Surgical Techniques
ClinicalTrials.gov ID: NCT06930378
What this study is testing
- What it's testing
- The goal of this clinical trial is to learn if nerve sutures in free flap breast reconstruction can optimize sensibility in the reconstructed breast in patients opting for DIEP flap breast reconstruction due to breast cancer or genetic conditions. Affected women 18 to 80 years old can be included.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 80, women only
You may be able to join if
- A) Pilot study
- 18-80 years old
- having received DIEP flap breast reconstruction with a flap not completely buried
- having given written informed consent for participating in the study
You likely can't join if
- postoperative radiotherapy on the flap
- neurological conditions as diabetic neuropathy, alcoholism or any other severe underlying peripheral neuropathy including chemotherapy-induced...
- active smoking
- language barrier
- pregnancy or lactating women B) Main study Inclusion Criteria:
- 18 to 80 years old
See the full eligibility criteria
- A) Pilot study
- 18-80 years old
- having received DIEP flap breast reconstruction with a flap not completely buried
- having given written informed consent for participating in the study
- postoperative radiotherapy on the flap
- neurological conditions as diabetic neuropathy, alcoholism or any other severe underlying peripheral neuropathy including chemotherapy-induced neuropathy or neuropathy induced by other medications
- active smoking
- language barrier
- pregnancy or lactating women B) Main study Inclusion Criteria:
- 18 to 80 years old
- having given written informed consent for participating in the study
- receiving immediate or delayed unilateral DIEP breast reconstruction with a DIEP flap which will not be completely buried Exclusion Criteria:
- autologous reconstruction where the flap is completely buried
- patients in need of both-sided reconstruction (double DIEP)
- postoperative radiotherapy on the flap
- neurological conditions as diabetic neuropathy, alcoholism, or any other severe underlying peripheral neuropathy including chemotherapy-induced neuropathy or neuropathy induced by other medications
- active smoking
- language barrier
- pregnancy at time of planned DIEP flap surgery and lactation
The study team makes the final eligibility decision.
Where it's taking place
- Geneva, Canton of Geneva, Switzerland
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling female, 18 years to 80 years. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Geneva, Canton of Geneva, Switzerland. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.