Clinical trial · Interventional
Bliss DTx Assessment During Course Care Including Port-A-Catheter Setting
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
Setting a Port-a Cath is performed in a surgical room, under ambulatory, by a specialist, under local anesthesia. This Port-a Cath is placed in the upper part of the thorax, under the clavicle, and facilitate the administration of certain anticancer drugs or to inject other treatments throughout the course of care. Setting a Port-a Cath is painful and stressful. In addition to local anesthesia, patients are often offered a sedation: anxiolytics, hypnotics or inhalation of MEOPA. Butterfly Therapeutics has developed a Digital Therapeutics (DTx) called Bliss DTx which uses virtual reality augmented by sound and visual stimuli. A first clinical study with Bliss DTx showed that the pain level was not significantly different between "Bliss DTx" arm and "MEOPA" arm when performing osteomedullary biopsy. This study is based on the hypothesis that Bliss DTx use would : * Be clinically equivalent to a standard protocol (use of hypnotics and/or anxiolytics and/or MEOPA and/or hypnosis conversational) to manage pain during Port-a Cath setting under local anesthesia * Reduce anxiety before setting a Port-a Cath * Provide greater satisfaction with the treatment process from patient point of view * Have organizational impacts, some of which could be economically valued
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Cancer | Malignant Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Pain management with BLISS DTx | Device | — | UNRESOLVED |
| Pain Management with site standard of care sedation protocol | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- BLISS Arm
- description
- Port-A-Cath setting under local anesthesia combined with Bliss DTx use
- interventionNames
- Device: Pain management with BLISS DTx
- type
- OTHER
- label
- GOLD STANDARD Arm
- description
- Port-A-Cath setting under local anesthesia combined with site standard of care sedation protocol
- interventionNames
- Other: Pain Management with site standard of care sedation protocol
Primary outcomes (3)
- measure
- Pain level
- timeFrame
- 1 day
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: * Patient, male or female, aged ≥ 18 years * Patient with a cancer diagnosis * Patient with Port-A-Cath setting under ambulatory * Patient affiliated to or beneficiary of a social security system * French speaking patient having signed informed consent Exclusion Criteria: * Patient with previous Port-A-Cath setting * Patient with pain perception disorder * Patient with contraindication to the use of virtual reality (VR) and screens * Pregnant woman * Protected patient
References
Publications (0)
Data not yet available