NCT04216992View on ClinicalTrials.gov

Value of Three-dimensional Rotational Epidurography on Percutaneous Epidural Adhesiolysis

CompletedOBSERVATIONAL
Enrollment

30

Participants

Timeline

Start Date

January 4, 2018

Primary Completion Date

October 24, 2019

Study Completion Date

December 6, 2019

Conditions
Failed Back Surgery SyndromeSpinal Stenosis
Interventions
DEVICE

Cone beam computed tomography

The contrast agent (Omnipaque, GE Healthcare, Ireland) was instilled to confirm the epidural space. With use of a calibrated angiographic C-arm system and a postprocessing workstation, we acquired volume data sets from two dimensional digital projection images obtained to reconstruct the 3D-RE during a C-arm rotation around the patient axis.

Trial Locations (1)

886

No. 325, Sec. 2, Cheng-kung Rd., Neihu 114, Taipei

All Listed Sponsors
lead

Tri-Service General Hospital

OTHER

NCT04216992 - Value of Three-dimensional Rotational Epidurography on Percutaneous Epidural Adhesiolysis | Biotech Hunter | Biotech Hunter