Menu
Recruiting NCT05779852

Pain Management of Amputation Wounds With AutoHypnosis

No phase Interventional Vascular Surgical Procedures

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: self-hypnosis and dressing, dressing.
Who it may be relevant to
Registry conditions: Vascular Surgical Procedures. Basic parameters: from 18 years · All.
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
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Amputation in vascular surgery mainly concerns the lower limb and is often linked to Obliterative Arterial Disease of the Lower Limbs. It indicates the impossibility or failure of revascularisation after an exhaustive assessment aimed at saving the limb. It is also performed to limit the spread of gangrene, an affection of the limb that can evolve into septicaemia. The principle is to amputate in a healthy and vascularised area to allow good healing of the amputation stump. Amputations of one, several or all toes, called complete transmetatarsal amputations, may take several months to heal. Amputations require directed healing and, above all, monitoring of the underlying tissues of the amputated area by daily detersions and wiping performed by a nurse at home. The mechanical detersion of the wound necessary for the healing process and cell migration, as well as optimal deep meshing, facilitate the evolution of the healing process. These treatments often cause pain, despite oral analgesics and local anaesthetics prior to the treatment. For several years, studies have shown the benefits of hypnosis in modifying the perception of pain, particularly during treatment. Studies have also shown that self-hypnosis allows a reduction in the intensity of pain. The clinical experience of the vascular surgery department of the University Hospital of Rennes suggests that patients who use self-hypnosis during the daily dressing of their amputation experience the moment more serenely, increasing their comfort and decreasing their pain and anxiety.

Interventions

  • Other self-hypnosis and dressing
    self-hypnosis during dressing
  • Other dressing
    dressing without self-hypnosis

Primary outcome measures

  • Level of pain [Time frame: Day 2 (during the 3rd post-operative amputation bandage)]

Eligibility criteria

Inclusion criteria

  • Age ≥ 18 years;
  • Naïve to amputation procedures;
  • Amputated, within 24 hours prior to inclusion, one, more or all toes
  • Pain level on the Numerical Scale ≥ 3 during the first dressing;
  • Affiliated to a social security scheme;
  • Having signed a free, informed and written consent.

Exclusion criteria

  • Cognitive impairments that limit understanding of instructions;
  • Cultural limitations reducing abstraction skills;
  • Previous practice of hypnosis;
  • Contraindications to hypnosis: Bipolar disorder or decompensated schizophrenia;
  • Chronic non-vascular pain;
  • Already in care for painful chronic wounds (ulcer wounds, bedsores...)
  • On morphine before surgery;
  • Analgesia by perineural catheter;
  • Protected person (adult subject to legal protection (safeguard of justice, curatorship, guardianship), person deprived of liberty, pregnant woman (declarative), nursing woman and minor).

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Single blind
Primary purpose
Other

Study locations

France · 1 center
  • CHU Rennes — Rennes

Identifiers

NCT: NCT05779852 · 35RC20_8896_MODOUPAAH · 2022-A00638-35

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗