Transient Elastography in Autoimmune Hepatitis
|
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
| ClinicalTrials.gov Identifier: NCT01905254 |
|
Recruitment Status :
Completed
First Posted : July 23, 2013
Results First Posted : May 6, 2015
Last Update Posted : May 6, 2015
|
- Study Details
- Tabular View
- Study Results
- Disclaimer
- How to Read a Study Record
| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Liver Cirrhosis | Device: Transient elastography (TE) Other: Liver biopsy | Not Applicable |
The aim of the current study was to assess the diagnostic performance of transient elastography for the determination of cirrhosis in patients with autoimmune hepatitis compared to the diagnosis of cirrhosis made on Laparoscopic guided liver biopsy. Patients referred for liver biopsy and transient elastography with a clinical diagnosis of AIH followed in the liver clinic of the Department of Gastroenterology at the UKE were prospectively included in the study.
Inclusion criteria were as follows: Confirmed diagnosis of AIH based on the diagnostic criteria revised by the International Autoimmune Hepatitis Group 2008 (20): 1. liver related autoantibodies, 2. hypergammaglobulinaemia, 3.typical histological findings and 4. absence of viral markers. Exclusion criteria were morbid obesity (BMI > 40), ascites, ileus or subileus, peritonitis, pregnancy, extrahepatic cholestasis and a severe inflammatory flare of AIH.
Blood liver tests including gamma-globulines, IgG, IgM, liver related autoantibodies (ANA, AMA, LKM, SMA, SLA) and viral markers (HBsAg, Anti HBs, Anti HBc, Anti HCV, Anti HAV) were performed before LB.
Each patient underwent abdominal ultrasound to exclude extrahepatic cholestasis prior to TE and minilaparoscopic liver biopsy. TE and minilaparoscopy were performed by physicians blinded to the results the other within a period of less than 3 months.
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 34 participants |
| Allocation: | N/A |
| Intervention Model: | Single Group Assignment |
| Masking: | Single (Investigator) |
| Primary Purpose: | Diagnostic |
| Official Title: | Prospective Comparison of Transient Elastography and Mini-laparoscopic Guided Liver Biopsy in Autoimmune Hepatitis |
| Study Start Date : | August 2007 |
| Actual Primary Completion Date : | August 2010 |
| Actual Study Completion Date : | January 2013 |
| Arm | Intervention/treatment |
|---|---|
|
Transient elastography and liver biopsy
All patients with Autoimmune hepatitis (AIH) were investigated with Transient Elastography before liver biopsy
|
Device: Transient elastography (TE)
TE and minilaparoscopic guided liver biopsy were performed by physicians blinded to the results the other within a period of less than 3 months. Other: Liver biopsy Minilaparoscopic guided liver biopsy was performed within a period of 3 months of Transient Elastography |
- Sensitivity and Specifity of Transient Elastography in Detection of Liver Cirrhosis [ Time Frame: Transient Elastography compared to liver histology ]The aim of the current study was to assess the diagnostic accuracy (Sens., Spec.) of transient elastography for the determination of cirrhosis in patients with autoimmune hepatitis. TE was compared to the diagnosis of cirrhosis made on histology yielded by laparoscopic guided liver biopsy.
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
| Ages Eligible for Study: | 18 Years to 80 Years (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Confirmed diagnosis of AIH based on the diagnostic criteria revised by the International Autoimmune Hepatitis Group 2008 (20):
- liver related autoantibodies,
- hypergammaglobulinaemia,
- typical histological findings and
- absence of viral markers.
Exclusion Criteria:
- morbid obesity (BMI > 40),
- ascites, ileus or subileus,
- peritonitis,
- pregnancy,
- extrahepatic cholestasis and
- a severe inflammatory flare of AIH.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01905254
| Germany | |
| Dept of Gastroenterology and Hepatology, University Medical Center Hamburg Eppendorf | |
| Hamburg, Germany, 20246 | |
| Principal Investigator: | Ulrike W Denzer, MD | Universitätsklinikum Hamburg-Eppendorf | |
| Study Chair: | Ansgar W Lohse, MD | Universitätsklinikum Hamburg-Eppendorf |
| Responsible Party: | PD Dr. med. Ulrike Denzer, Attending physician, Universitätsklinikum Hamburg-Eppendorf |
| ClinicalTrials.gov Identifier: | NCT01905254 |
| Other Study ID Numbers: |
UKE IRB 2742 |
| First Posted: | July 23, 2013 Key Record Dates |
| Results First Posted: | May 6, 2015 |
| Last Update Posted: | May 6, 2015 |
| Last Verified: | May 2015 |
|
Transient elastography mini-laparoscopy liver biopsy liver cirrhosis autoimmune hepatitis |
|
Hepatitis Liver Cirrhosis Hepatitis, Autoimmune Fibrosis Liver Diseases |
Digestive System Diseases Pathologic Processes Hepatitis, Chronic Autoimmune Diseases Immune System Diseases |

