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145 studies found for:    "Portal hypertension"
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Rank Status Study
1 Unknown  MRI in Portal Hypertension
Condition: Portal Hypertension
Intervention: Procedure: MRI Scan
2 Not yet recruiting Treatment of Low-grade Cirrhotic Portal Hypertension Due to Hepatitis B Virus With Fuzheng Huayu and Entecavir
Condition: Portal Hypertension
Interventions: Drug: Entecavir + Placebo;   Drug: Entecavir + Fuzheng Huayu
3 Not yet recruiting Treatment of Moderate and Severe Cirrhotic Portal Hypertension Due to HBV With Traditional Chinese Medicine and Entecavir
Condition: Portal Hypertension
Interventions: Drug: Entecavir+Carvedilol+ Placebo;   Drug: Entecavir+Carvedilol+ Fuzheng Huayu;   Drug: Entecavir+Carvedilol+ Fuzheng Huayu +TCM analysis
4 Completed Comparison of Endoscopic Variceal Ligation (EVL) With Propranolol in Non Cirrhotic Portal Hypertension (NCPH)
Condition: Non Cirrhotic Portal Hypertension
Interventions: Drug: Propranolol;   Device: multi band ligator for esophageal varices
5 Completed
Has Results
An Exploratory Haemodynamic Study in Patients With Compensated Cirrhosis and Portal Hypertension
Condition: Compensated Cirrhosis and Portal Hypertension
Interventions: Drug: Terlipressin acetate;   Drug: Serelaxin (RLX030)
6 Completed Risk Factors for Variceal Bleeding in Egyptian Patients With Non-Cirrhotic Portal Hypertension
Condition: Portal Hypertension
Intervention: Procedure: Upper gastrointestinal endoscopy
7 Terminated
Has Results
Efficacy and Safety of Cobiprostone in Patients With Portal Hypertension
Condition: Portal Hypertension
Interventions: Drug: Placebo;   Drug: Cobiprostone
8 Recruiting Doppler Ultrasound Hepatic Vein Waveform as a Non-invasive Tool in the Assessment of Severity of Portal Hypertension
Condition: Portal Hypertension
Intervention: Drug: Carvedilol
9 Recruiting A Study to Investigate the Effect of the Study Drug (FE 204205) in Patients With Cirrhotic Portal Hypertension
Condition: Portal Hypertension
Interventions: Drug: FE 204205;   Drug: Placebo
10 Recruiting Non-invasive Diagnosis of Portal Hypertension With Acoustic Radiation Force Impulse (ARFI)
Conditions: Portal Hypertension;   Chronic Liver Disease
Intervention: Device: ARFI ultrasound
11 Recruiting Laparoscopic Versus Open Devascularization for Portal Hypertension, a Randomized Controlled Trial
Conditions: Portal Hypertension;   Liver Cirrhosis
Interventions: Procedure: open surgical procedure;   Procedure: laparoscopic surgical procedure
12 Completed Assessing Outcome After H-graft Shunt Placement
Condition: Portal Hypertension
Intervention: Other: Chart Review
13 Completed Danish Carvedilol Study in Portal Hypertension
Conditions: Cirrhosis;   Portal Hypertension
Interventions: Drug: carvedilol;   Drug: propranolol
14 Recruiting Value of Von Willebrand Factor in Portal Hypertension
Conditions: Liver Cirrhosis;   Portal Hypertension
Intervention:
15 Completed Microparticles in Cirrhosis and Portal Hypertension
Conditions: Liver Cirrhosis;   Portal Hypertension
Intervention: Other: research on interactions between portal hypertension and microparticles
16 Completed
Has Results
Probiotics for Liver Cirrhosis With Portal Hypertension
Conditions: Liver Cirrhosis;   Portal Hypertension
Interventions: Dietary Supplement: GK#10;   Drug: Placebo
17 Recruiting Noninvasive Subharmonic Aided Pressure Estimation of Portal Hypertension
Conditions: Liver Diseases;   Portal Hypertension
Intervention: Drug: SHAPE measurement (Sonazoid ultrasoud contrast agent)
18 Not yet recruiting Spironolactone on Fibrosis Progrssion-Portal Hypertension(FP-PH)in Cirrhosis
Conditions: Cirrhosis;   Portal Hypertension
Interventions: Drug: Spironolactone;   Drug: Carvedilol
19 Recruiting Viatorr CX Case-control Study for Complications of Portal Hypertension
Conditions: Liver Cirrhoses;   Portal Hypertension
Intervention: Device: TIPS
20 Recruiting Study to Assess Safety and Efficacy of Ifetroban for Treatment of Portal Hypertension in Cirrhotic Patients
Conditions: Portal Hypertension;   Liver Cirrhosis
Interventions: Drug: Ifetroban;   Drug: Placebo

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Study has passed its completion date and status has not been verified in more than two years.