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96 studies found for:    "progressive familial intrahepatic cholestasis" OR "Cholestasis, Intrahepatic"
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Rank Status Study
1 Active, not recruiting Open Label Study to Evaluate Efficacy and Long Term Safety of LUM001 in the Treatment of Cholestatic Liver Disease in Patients With Progressive Familial Intrahepatic Cholestasis
Condition: Progressive Familial Intrahepatic Cholestasis (PFIC)
Intervention: Drug: LUM001
2 No longer available Buphenyl Therapy for Byler's Disease
Condition: Byler Disease
Intervention: Drug: Buphenyl
3 No longer available Transition From Buphenyl to RAVICTI for the Therapy of Byler Disease
Condition: Byler Disease
Intervention: Drug: Glycerol phenylbutyrate
4 Temporarily not available Expanded Access Protocol for an Intermediate Size Population - RAVICTI for Byler Disease
Condition: Byler Disease
Intervention: Drug: RAVICTI
5 Completed Induction of Labor in Intrahepatic Cholestasis of Pregnancy
Condition: Intrahepatic Cholestasis
Intervention:
6 Withdrawn The Use of Fish Oil Supplementation in Treatment of Intrahepatic Cholestasis of Pregnancy
Condition: Intrahepatic Cholestasis of Pregnancy
Intervention: Dietary Supplement: Fish Oil Supplement Group
7 Unknown  Il-17 Levels in Intrahepatic Cholestasis of Pregnancy
Condition: Intrahepatic Cholestasis of Pregnancy
Intervention:
8 Completed ABCB4 Gene Mutations in Intrahepatic Cholestasis of Pregnancy and Controls
Condition: Intrahepatic Cholestasis of Pregnancy
Intervention:
9 Completed Ursodeoxycholic Acid in the Treatment of Intrahepatic Cholestasis of Pregnancy
Conditions: Intrahepatic Cholestasis;   Pregnancy
Interventions: Drug: ursodeoxycholic acid;   Drug: Placebo
10 Completed Validation of the Itch Reported Outcome (ItchRO) Diaries in Pediatric Cholestatic Liver Disease
Conditions: Alagille Syndrome;   Progressive Familial Intrahepatic Cholestasis
Intervention:
11 Completed Study With Heptral in Subjects With Liver Disease Due to Alcohol Consumption
Condition: Intrahepatic Cholestasis Associated With Alcoholic Liver Disease
Interventions: Drug: Ademetionine IV+tablet;   Drug: Ademetionine tablet
12 Recruiting The Metabolic Profile in Intrahepatic Cholestasis of Pregnancy and Diabetes Mellitus
Conditions: Intrahepatic Cholestasis of Pregnancy;   Gestational Diabetes Mellitus
Intervention:
13 Withdrawn Ursodeoxycholic Acid And Cholestasis Of Pregnancy
Condition: Intrahepatic Cholestasis of Pregnancy
Interventions: Drug: Ursodeoxycholic Acid;   Drug: Placebo
14 Completed A Study to Evaluate the Safety, Tolerability, Pharmacokinetics (PK) and Pharmacodynamics (PD) of Repeat Doses of GSK2330672 Administration in Subjects With Primary Biliary Cirrhosis (PBC) and Symptoms of Pruritus
Condition: Cholestasis, Intrahepatic
Interventions: Drug: GSK2330672;   Drug: Placebo;   Drug: Ursodeoxycholic acid
15 Recruiting Serum Autotaxin Levels in Cholestasis of Pregnancy
Condition: Intrahepatic Cholestasis of Pregnancy
Intervention:
16 Unknown  P-wave Duration and Dispersion in Intrahepatic Cholestasis of Pregnancy
Conditions: Intrahepatic Cholestasis of Pregnancy;   Arrhythmia
Intervention:
17 Completed A Safety and Pharmakokinetic Study of A4250 Alone or in Combination With A3384
Conditions: Orphan Cholestatic Liver Diseases;   Primary Biliary Cirrhosis;   Progressive Familial Intrahepatic Cholestasis;   Alagille Syndrome
Interventions: Drug: A4250;   Drug: CRC (A3384);   Drug: Questran;   Drug: Placebo
18 Recruiting Evaluating the Genetic Causes and Progression of Cholestatic Liver Diseases (LOGIC)
Conditions: Liver Diseases;   Alagille Syndrome;   Alpha 1-Antitrypsin Deficiency
Intervention:
19 Terminated Second-line Therapy of Unresectable Cholangiocarcinoma by RADIOEMBOLIZATION
Condition: Cholestasis, Progressive Familial Intrahepatic 3
Intervention: Device: Yttrium microsphere injection
20 Recruiting Retrospective Study About Primary Biliary Cholangitis During January 2001 to July 2016 at West China Hospital
Conditions: Cholangitis;   Liver Cirrhosis, Biliary;   Cholestasis;   Liver Diseases;   Liver Cirrhosis;   Bile Duct Diseases
Intervention:

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