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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03599492
Other study ID # 16-01360
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 2016
Est. completion date April 12, 2022

Study information

Verified date August 2022
Source NYU Langone Health
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The effect of portal hypertension on gastrointestinal motility, and how reversal or improvement in portal hypertension may alter gastrointestinal motility, remains unclear and further research is needed. Additionally, patients with cirrhosis have altered gut microflora, particularly rich in lactobacilli, including enterococci and bifidobacteria. Transjugular Intraheptic Portosystemic Shunting (TIPS) is a procedure performed by interventional radiologists, in which a connection is made between the portal and venous circulations, allowing high pressure portal blood to more easily enter the systemic circulation and bypass the liver; thus effectively decreased portal pressure.


Recruitment information / eligibility

Status Completed
Enrollment 14
Est. completion date April 12, 2022
Est. primary completion date April 12, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 99 Years
Eligibility Inclusion Criteria: - Patients with either radiographic or biopsy proven decompensated cirrhosis (as determined by ascites, variceal hemorrhage, encephalopathy or jaundice). - Patients undergoing an elective TIPS for any standard of care established indication (examples: worsening ascites, recurrent variceal bleeding). Exclusion Criteria: - Pregnant women. - Patients unwilling or unable to provide informed consent. - Patients undergoing an emergent TIPS for acute or subacute variceal hemorrhage. - Patients with diabetes, significant cardiovascular, renal or other chronic disease which has been known to affect intestinal motility. - Previously diagnosed gastroparesis or other GI dysmotility disorder. - Patients currently taking narcotics, antibiotics excluding rifaximin, prokinetic medications or lactulose. - Patients with a history of gastric bezoar. - Patients with a history of multiple intestinal surgeries or GI surgery within the past 3 months. - Patients with a history of gastrointestinal strictures, fistulas, or physiological or mechanical obstruction. - Patients with a history of gastrointestinal strictures, fistulas, or physiological or mechanical obstruction. - Patients with a history of gastrointestinal strictures, fistulas, or physiological or mechanical obstruction. - Patients with a history of diverticulitis. - Patients with swallowing disorders and increased risk of aspiration (such as prior history of aspiration). - Patient with Celiac disease. - Patients with implanted or portable electro-mechanical medical devices.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
SMART Pill Pre-TIPS
Assessment of motility with Smart Pill, which will be read and confirmed by gastroenterologist trained to interpret motility studies
SMART Pill Post TIPS
Assessment of motility with Smart Pill, which will be read and confirmed by gastroenterologist trained to interpret motility studies

Locations

Country Name City State
United States NYU Langone Health New York New York

Sponsors (1)

Lead Sponsor Collaborator
NYU Langone Health

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pre-TIPS intestinal transit time (measured in hours and minutes), via smart pill in patients with cirrhosis Due to small sample size, Wilcoxon rank-sum test will be used to compare the continuous variable of gut transit times. A p-value of <0.05 will be considered statistically significant. 14 Weeks
Primary Post TIPS intestinal transit time (measured in hours and minutes), via smart pill in patients with cirrhosis Due to small sample size, Wilcoxon rank-sum test will be used to compare the continuous variable of gut transit times. A p-value of <0.05 will be considered statistically significant. 14 Weeks
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