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New treatment option for Amputation
Official title Early Evaluation of the Introduction of Pre- and Post-operative Psychological and Physiotherapeutic Follow-up in Vascular Surgery in Amputee Patients
ClinicalTrials.gov ID: NCT04750876
What this study is testing
- What it's testing
- An amputation represents a real ordeal for the person who will have to overcome the loss of a limb and face long months of rehabilitation. It is most often carried out following arterial insufficiency.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join if
- Patient over the age of majority, no age limit
- Amputation related to obliterative arteriopathy of the lower limbs
- Trans-tibial or trans-femoral amputation
- Patient with an indication of discharge to a rehabilitation and re-education service
- Patient with the ability to understand the protocol
You likely can't join if
- Trauma related amputation
- Amputation of upper limb, trans-metatarsal or one or more toes
- Amputation of comfort in a palliative care setting
- Patient leaving home after surgery
- Patient undergoing psychological or psychiatric treatment
- Pregnant or breastfeeding woman, or a woman who is able to procreate without effective contraception
See the full eligibility criteria
- Patient over the age of majority, no age limit
- Amputation related to obliterative arteriopathy of the lower limbs
- Trans-tibial or trans-femoral amputation
- Patient with an indication of discharge to a rehabilitation and re-education service
- Patient with the ability to understand the protocol
- Patient who has agreed to participate in the study and has given express oral consent
- Patient receiving social security cover or entitled to it
- Trauma related amputation
- Amputation of upper limb, trans-metatarsal or one or more toes
- Amputation of comfort in a palliative care setting
- Patient leaving home after surgery
- Patient undergoing psychological or psychiatric treatment
- Pregnant or breastfeeding woman, or a woman who is able to procreate without effective contraception
- Patient unable to follow the protocol as judged by the investigator
- Patient participating in another treatment research protocol involving a drug or medical device
- Patient under guardianship, curators or legal protection measure
The study team makes the final eligibility decision.
Where it's taking place
- La Roche-sur-Yon, France
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 all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include La Roche-sur-Yon, France. 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.