MedPath

Trial Evaluating Hypnosis Using Virtural Reality vs Standard Pain Management During Musculoskelettal Biopsy

Not Applicable
Completed
Conditions
Musculoskeletal Cancers
Interventions
Procedure: Deep local anesthesia + Virtual reality
Procedure: Deep local anesthesia alone
Registration Number
NCT03418597
Lead Sponsor
Centre Leon Berard
Brief Summary

The primary objective of this trial is to evaluate the benefit of the virtual reality technology in the pain management for patients having a radio-guided musculoskeletal biopsy indication

Detailed Description

During the last years, the percutaneous biopsies took a growing importance in the diagnosis of musculoskeletal cancers. The most important advantages of percutaneous biopsies are: 1) Often performed under local anesthesia in out-patient department, 2) No visible scars, 3) Surgical intervention avoided in case of benign tumor with a low level of complications (infection, hematoma, pain).

The technology improvement of percutaneous biopsy leads to a high diagnosis success rate (80.8% for bone tumors and 83.2% for soft tissues tumors') with a low complication rate (0.7%) and then justifies the use of percutaneous biopsy as first-line diagnostic exam.

During a percutaneous biopsy, the pain is frequently felt with an increase in the "pain numeric scale" evaluated after the procedure.

The nitrous oxide is a gas mixture which can be used for its anesthetic and antalgic properties, making the pain tolerable for the patients during short procedures. However, it can cause adverse events such as nausea, vomiting and nervous system affections (excessive sedation, anxiety). Moreover, this gas is not always efficient for the pain management.

Other options have been investigated such as hypnosis and music therapy which improve patients' experience of the medical interventional procedures.

The virtual reality is a digital tool existing for about 10 years. It enables to isolate a patient from the real world which can be useful in some medical indications. It is a 3-D immersive experience, created using a visual and audio headset. Virtual reality can reduce the pain experienced during surgical interventions and has widely shown its interest in algogenic cares.

While the results are promising, a recent review of the literature shows that very few randomized clinical trials document the virtual reality benefit in pain and/or anxiety management for burn patients or patients suffering from acute or chronic pains.

The objective of this study is to demonstrate the benefit of the virtual reality in addition to a deep local anesthesia vs a deep local anesthesia alone in the pain management linked to musculoskeletal tumors biopsy.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
99
Inclusion Criteria
  • Man or woman, aged >= 18 years at the day of consenting to the study (no upper limit)
  • Requiring a radio-guided biopsy of the musculoskeletal system,
  • Informed and signed consent,
  • Patient covered by a medical insurance.
Exclusion Criteria
  • Deaf patient;
  • Visually-impaired patient;
  • Claustrophobic and/or aquaphobic patient;
  • Contraindication to a musculoskeletal biopsy, including to the premedication protocol and to the lidocaine;
  • Person deprived of liberty or placed under guardianship;
  • Absence of French language skills;
  • History of psychiatric disease such as paranoia, schizophrenia, manic-depressive psychosis, patient with a high risk of suicide.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Deep local anesthesia + Virtual realityDeep local anesthesia + Virtual realityPre-medication procedures and lidocaïne injection are the same as in the current practice. During the intervention delay, the patient will also experience hypnosis through a virtual reality procedure .
Deep local anesthesia aloneDeep local anesthesia aloneThe musculoskeletal biopsy is performed according to the standard practice using a deep local anesthesia with premedication and lidocaïne.
Primary Outcome Measures
NameTimeMethod
Evaluate the benefit of the virtual reality in the pain management of patients needing a radio-guided musculoskeletal biopsy.Day 0

The main outcome will be the pain level auto-evaluated by the patient using a numeric scale composed of 11 graduations (from 0 to 10)

Secondary Outcome Measures
NameTimeMethod
Evaluate the global satisfaction of patients in both armsDay 0

The score "0" corresponds to " Absence of satisfaction " and the score " 10 " corresponds to " Full satisfaction ".

Evaluate the analgesics consumption in both armsthrough study completion, an average of 24 hours

Evaluation according to the following classification and recording the dosages and units taken: Level 1 - Non morphinic analgesics; Level 2 - Weak opioides analgesics; Level 3 - Strong opioides analgesic

Evaluate in both arms, the pain linked to the biopsy procedure using a numeric scale graduated from 0 to 10.Day 1 (+/-2h) post biopsy

The score " 0 " corresponds to " No pain " and the score " 10 " corresponds to " Maximum amount of imaginable pain "

Evaluate in both arms, the anxiety linked to the biopsy procedure using a numeric scale graduated from 0 to 10Day 0

The score " 0 " corresponds to " No anxiety " and the score " 10 " corresponds to " Maximum imaginable anxiety "

Evaluate costs in both armsthrough study completion, an average of 24 hours

Evaluation of costs involved for the patient's treatment and care

Trial Locations

Locations (1)

Centre Leon Berard

🇫🇷

Lyon, France

© Copyright 2025. All Rights Reserved by MedPath