Clinical trial · Interventional
Algology in Oncology Osteopathic Support (ALGOS)
Algology in Oncology Osteopathic Support
NCT05726929CI-TRIAL-00086167ALGOScompletedN/AClinicalTrials.gov clinicaltrialsProvenance
- 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)
The aim of the study is to evaluate the Impact of add-on osteopathic treatment in the algological course of patients treated for breast cancer : Randomized Controlled Trial.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
| Neuropathic Pain | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Capsaicin QUTENZA Patch (TAU) | Other | — | UNRESOLVED |
| Osteopathic treatment | Other | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Osteopathic treatment (OT)
- description
- Osteopathic treatment, 3 sessions of 1h + Treatment As Usual (TAU)
- interventionNames
- Other: Osteopathic treatment
- Other: Capsaicin QUTENZA Patch (TAU)
- type
- ACTIVE_COMPARATOR
- label
- Treatment As Usual (TAU)
- description
- Treatment As Usual, Capsaicin Qutenza Patch (Conventionnal Treatment in algology in supportive care)
- interventionNames
- Other: Capsaicin QUTENZA Patch (TAU)
Primary outcomes (1)
- measure
- Changes in Neuropathic pain assessment from baseline to 9 months
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 80 Years
Show eligibility criteria text
Inclusion Criteria: * Major patients with sequelae of pain following breast cancer surgery with or without other treatments and who have been in pain for more than 3 months. Neuropathic pain may be experienced in the upper and middle chest, armpit and/or arm ipsilateral to the surgery and/or radiotherapy. Exclusion Criteria: * Unemancipated minors, protected adults and adults who are not in a position to give their consent are excluded from the protocol. * Patients who do not have social security coverage * Patients with non-iatrogenic peripheral neuropathy * Patients who do not speak French * Patients with confusional disorders * Patients with a brain tumour * Any patient with healing disorders at the surgical site
References
Publications (0)
Data not yet available
No reference posted for this study.