General information
  • Disease category Other Cancer (BASEC)
  • Recruitment status recruitment completed (BASEC/ICTRP)
  • Trial sites
    Geneva
    (BASEC)
  • Contact Sana Boudabbous Sana.boudabbous@hcuge.ch (BASEC)
  • Data Source(s) BASEC: Import from 20.03.2025 ICTRP: N/A
  • Last update 20.03.2025 09:55
HumRes55296 | SNCTP000004423 | BASEC2020-02998

HIFU META BONE HYPERTHERMIA

  • Disease category Other Cancer (BASEC)
  • Recruitment status recruitment completed (BASEC/ICTRP)
  • Trial sites
    Geneva
    (BASEC)
  • Contact Sana Boudabbous Sana.boudabbous@hcuge.ch (BASEC)
  • Data Source(s) BASEC: Import from 20.03.2025 ICTRP: N/A
  • Last update 20.03.2025 09:55

Summary description of the study

HIF FOR BOEN META AS ADJUVANT HYYPERTHERMIA BEFORE RADIOTHERAPY TO IMPROVE RADIOTHERAPY EFFECT

(BASEC)

Intervention under investigation

HIFU UNDER MR guidance

(BASEC)

Disease under investigation

METASTASES OF BONE

(BASEC)

Criteria for participation in trial
bone meta in limbs and pelvis with cortical defect 5cm or less in diameter (BASEC)

Exclusion criteria
spine and no bone defect and CI of MRI (BASEC)

Trial sites

Geneva

(BASEC)

not available

Sponsor

NOT APPLICABLE

(BASEC)

Contact

Contact Person Switzerland

Sana Boudabbous

+41795532444

Sana.boudabbous@hcuge.ch

HUG

(BASEC)

Scientific Information

not available

Name of the authorising ethics committee (for multicentre studies, only the lead committee)

Ethics Committee Geneva

(BASEC)

Date of authorisation

21.05.2021

(BASEC)


ICTRP Trial ID
not available

Official title (approved by ethics committee)
Pain relief in patients with symptomatic bone metastases: a feasibility pilot study on palliative radiotherapy with adjuvant hyperthermia by magnetic resonance-guided focused ultrasound. (BASEC)

Academic title
not available

Public title
not available

Disease under investigation
not available

Intervention under investigation
not available

Type of trial
not available

Trial design
not available

Inclusion/Exclusion criteria
not available

not available

Primary and secondary end points
not available

not available

Registration date
not available

Incorporation of the first participant
not available

Secondary sponsors
not available

Additional contacts
not available

Secondary trial IDs
not available

Results-Individual Participant Data (IPD)
not available

Further information on the trial
not available

Results of the trial

Results summary

not available

Link to the results in the primary register

not available