Trials / Unknown
UnknownNCT06336850
Safety and Efficacy of Endoscopic Ultrasound-Guided Portal Pressure Gradient Measurement
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 100 (estimated)
- Sponsor
- Methodist Health System · Academic / Other
- Sex
- All
- Age
- 18 Years – 85 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate the efficacy, safety, and adequacy of Endoscopic Ultrasound (EUS) Portal Pressure Gradient Measurement (PPGM) in patients undergoing EUS-guided liver biopsies.
Detailed description
Patients undergoing EUS-guided liver biopsy may qualify to participate in this study. The purpose of this study is to evaluate the efficacy, safety, and adequacy of EUS- Portal Pressure Gradient Measurement (PPGM) in patients with liver disease referred for EUS-guided liver biopsy.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Endoscopic Ultrasound-Guided Portal Pressure Gradient Measurement | The endoscopic ultrasound (EUS)-guided 25G fine needle aspirate (FNA) needle procedure is a straightforward minimally invasive technique for direct portal pressure measurements. |
Timeline
- Start date
- 2020-12-23
- Primary completion
- 2025-01-01
- Completion
- 2025-01-01
- First posted
- 2024-03-29
- Last updated
- 2024-03-29
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT06336850. Inclusion in this directory is not an endorsement.