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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT05075148
Other study ID # RECHMPL21_0029
Secondary ID
Status Enrolling by invitation
Phase
First received
Last updated
Start date January 1, 2021
Est. completion date March 30, 2022

Study information

Verified date July 2021
Source University Hospital, Montpellier
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study aims to describe the clinical outcomeand the radiological appearance of aneurysmal bone cyst treated by means of interventional radiology procedures (percutaneous sclerosis and endovascular embolization)


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 20
Est. completion date March 30, 2022
Est. primary completion date December 1, 2021
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion criteria: - Male of female - Aging from 0 to 30 years - With typical aneurysmal bone cyst at initial imaging - At least one interventional radiology procedure performed Exclusion criteria: - No initial surgery - Patient refuses to participate

Study Design


Related Conditions & MeSH terms


Intervention

Other:
radiology
Interventional radiology for aneurysmal bone cyst ( percutaneous alcoholization, vascualr embolisation)

Locations

Country Name City State
France Uhmontpellier Montpellier

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Montpellier

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Difference of size lesion after treatement Percentage of peripheral reossification after treatment :
0%: no reossification
< 25%: low reossification
Between 25% -50%: Partial reossification
Between 50-75%: significant reossification
> 75%: very significant reossification
100%: complete reossifcation
day 1
Secondary Number of pain Pain measured with Pain scale ( 0 = no pain , 10 = maximum pain) day 1
Secondary number of deficience Number of patients needs second treatment 3- Fracture ? (yes or no) day 1
Secondary number of complication Fracture ? (yes or no) day 1
See also
  Status Clinical Trial Phase
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Completed NCT03076138 - Gene-activated Bone Substitute for Maxillofacial Bone Regeneration N/A
Withdrawn NCT00459641 - Safety and Tolerability of I-040302 in Children and Young Adults With Solitary Bone Cysts Phase 2
Recruiting NCT05880628 - Evaluation of Faisability, Safety and Effectiveness and of Discogel in Patients With Aneurysmal and Simple Bone Cysts