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Multi-modality Evaluation of Flow Rate, Pressure and Size of Spine Epidural Venous Plexus

Multi-modality Evaluation of Flow Rate, Pressure and Size of Spine Epidural Venous Plexus

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05519618
Enrollment
32
Registered
2022-08-29
Start date
2022-08-01
Completion date
2023-07-31
Last updated
2022-08-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Neoplasms, Spine Tumor, Venous Hypertension

Keywords

Spine tumor, Venous pressure, Internal vertebral venous plexus, Epidural venous plexus

Brief summary

Vertebra is one of the most common site of metastatic disease, which may cause severe pain or neurological deficit. Debulking surgery usually has better local control and survival benefit as compared with decompression or radiotherapy. However, debulking surgery often accompany with massive blood loss, which may cause hemorrhagic shock or death. The major bleeding point during operation including tumor parenchyma, arteries that are difficult to ligate, and epidural venous plexus. Vascularity of tumor parenchyma had been associated with increased intraoperative blood loss, on the other hand, there is a lack in the literature regarding to evaluation of the size, flow and pressure of epidural venous plexus, and their changes after embolization.

Interventions

PROCEDUREEpidural veins pressure and flow measurement

The purpose of this study is to measure to pressure and flow of epidural venous plexus. The procedure will be performed alongside during pre-operative embolization at the angiography suite. It will be performed under general anesthesia. A the start of the procedure, a venous access will be established at the inguinal region. Co-axial catheters will be navigated to epidural venous plexus under the guidance of fluoroscopy. After the placement of catheter, the pressure and flow of epidural venous plexus will be measured at three time points: 1. Right after catheter reach the targeted location 2. Right before embolization. 3. After embolization. The participant will be instructed to control their breathe during measurement. After measurement, the catheter will be removed alongside with embolization devices, and achieved hemostasis as routine.

Sponsors

Ministry of Science and Technology, Taiwan
CollaboratorOTHER_GOV
National Taiwan University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Patient who receive pre-operative angiography and possible embolization before debulking surgery or en bloc resection of the spinal tumor. 2. The tumor has to be located in thoracic or lumbar spine.

Exclusion criteria

1. Confirmed non-tumor diagnosis. 2. Patient who cannot tolerate the procedure due to severe pain. 3. Patients who cannot receive angiography or embolization due to contraindications, including poor renal function (Serum creatinine \>2.0 deciliter/mg or estimated glomerular filtration rate(eGFR)) \< 30ml/min) , severe allergy to contrast medium, uncorrectable coagulopathy and bleeding diathesis. 4. Patient who has severe neurological deficit that should receive emergent decompression. 5. Poor image quality. 6. Expected life expectancy \< 6 months.

Design outcomes

Primary

MeasureTime frameDescription
Epidural venous pressureDuring the embolization intervention.Epidural venous pressure measured with pressure wire after reach the targeted location, before embolization and after embolization during the embolization procedure.
Epidural venous flow rate.During the embolization intervention.Epidural venous flow rate measured with fluoroscopy after reach the targeted location, before embolization and after embolization during the embolization procedure.

Secondary

MeasureTime frameDescription
Size of epidural venous plexus.During the embolization intervention.Measuring the size of epidural venous plexus with fluoroscopy after reach the targeted location, before embolization and after embolization during the embolization procedure.

Countries

Taiwan

Contacts

Primary ContactYuCheng Huang, M.D.
squll1peter@gmail.com+886223123456

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026