Midodrine and Albumin in Patients With Refractory Ascites
Primary Purpose
Refractory Ascites
Status
Unknown status
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Albumin
Midodrine
Standard medical therapy (SMT)
Sponsored by
About this trial
This is an interventional treatment trial for Refractory Ascites
Eligibility Criteria
Inclusion Criteria:
- Age between 18 and 80 years
- Refractory ascites in cirrhosis of any etiology
Exclusion Criteria:
- Mixed ascites: cirrhosis plus another cause of ascites
- Gastrointestinal bleed within 7 days of enrolment.
- Presence of hepatorenal syndrome
- Hepatic encephalopathy grade 2 or higher
- Infection within 1 month preceding the study
- Cardiovascular disease (ejection fraction < 35% or abnormal ECG) or arterial hypertension (BP > 140/90 mm of Hg)
- Abnormal urine analysis with proteinuria > 500 mg/24 hour or 50 red blood cells/high power field, or granular casts or ultrasonographic evidence of intrinsic renal disease
- Presence of hepatocellular carcinoma or portal vein thrombosis
- Treatment with drug with known effects on systemic and renal hemodynamics within 7 days of inclusion excepting beta-blockers
- Patient not willing for study.
- Patient opting for liver transplantation/ transjugular intrahepatic portosystemic shunt
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
Placebo Comparator
Arm Label
Albumin + Midodrine + SMT
Albumin + SMT
SMT
Arm Description
Human albumin plus oral midodrine
Human albumin plus placebo of midodrine
standard medical therapy plus placebo of midodrine
Outcomes
Primary Outcome Measures
Number of patients with control of ascites at 1 year
Control of ascites will be defined as-
Complete response will be total absence of ascites.
Partial response as presence of ascites not requiring paracentesis
Non response will be defined as persistence of severe ascites requiring paracentesis.
Secondary Outcome Measures
Change in estimated glomerular filtration rate (eGFR) measured by modified diet in renal disease 6 (MDRD6) formula at 3 months intervals
eGFR will be measured using MDRD6 formula
Changes in concentration of albumin at 3 months intervals
Change in concentration of serum albumin (g/dl)
Change in model for end stage liver disease (MELD) score
Change in MELD score. The MELD score incorporates the variables of serum bilirubin, creatinine and Internation Normalised Ratio (INR). Higher MELD score indicates worse prognosis
Change in mean arterial pressure at 3 months interval
Change in mean arterial pressure (mm of Hg) will be noted
Changes in serum and 24- hour urine sodium
Serum and urine sodium concentration will be measured in meq/L
Incidence of spontaneous bacterial peritonitis (SBP) and other infections
The diagnosis of SBP will be based on neutrophil count in ascitic fluid of >250/mm3 as determined by microscopy and positive ascitic fluid culture or >250 /mm3 with negative culture called as culture negative neutrocytic ascites.20 Other infections will be diagnosed as per CDC criteria.
Number of patients who develop paracentesis induced circulatory dysfunction (PICD)
PICD will be defined as an increase in plasma renin activity (PRA) of >50% of the pre-treatment value to a level > 4ng/ml/hr on 6th day after paracentesis
Number of patients who develop hyponatremia
Hyponatremia will be defined using serum sodium concentrations of <130meq/L.
Change in Child-Turcotte-Pugh (CTP) score
Change in CTP score. The CTP score incorporates the variables of serum bilirubin, albumin, prothrombin time-INR, grade of ascites and hepatic encephalopathy. The score ranges from 5-15 and a higher score portends a worse prognosis
Number of patients who develop hypokalemia
Hypokalemia will be defined using serum potassium levels <3 meq/L
Number of patients who develop hyperkalemia
hyperkalemia will be defined using serum potassium levels >6 meq/L
Full Information
NCT ID
NCT04621617
First Posted
October 27, 2020
Last Updated
November 3, 2020
Sponsor
Postgraduate Institute of Medical Education and Research
1. Study Identification
Unique Protocol Identification Number
NCT04621617
Brief Title
Midodrine and Albumin in Patients With Refractory Ascites
Official Title
Midodrine and Albumin in Patients With Refractory Ascites. A Randomised Controlled Trial.
Study Type
Interventional
2. Study Status
Record Verification Date
November 2020
Overall Recruitment Status
Unknown status
Study Start Date
November 2020 (Anticipated)
Primary Completion Date
December 2021 (Anticipated)
Study Completion Date
April 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Postgraduate Institute of Medical Education and Research
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Refractory ascites is seen in 5-10% of patients with cirrhosis.Decompensated cirrhosis with refractory ascites has a mortality rate of around 40% in a year and a median survival of 6 months.Portal hypertension and splanchnic vasodilation are major factors in the development of ascites.The treatment of refractory ascites involves salt restriction, diuretics, large volume paracentesis (LVP), transjugular Intrahepatic Portosystemic shunt (TIPS) and Liver Transplantation (LT). Currently the only curative treatment is LT. However, LT is limited due to organ shortage and high cost.
Long-term human albumin (HA) administration in patients with uncomplicated and refractory ascites, has shown to improve survival or delay the complications of cirrhosis. Midodrine, an oral α1- adrenergic agonist has been used in refractory ascites with variable results. However, there is no study on the use of long term Midodrine and HA in patients with refractory ascites. Therefore, we plan to study the effect of long term midodrine and HA in patients with refractory ascites.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Refractory Ascites
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
114 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Albumin + Midodrine + SMT
Arm Type
Active Comparator
Arm Description
Human albumin plus oral midodrine
Arm Title
Albumin + SMT
Arm Type
Active Comparator
Arm Description
Human albumin plus placebo of midodrine
Arm Title
SMT
Arm Type
Placebo Comparator
Arm Description
standard medical therapy plus placebo of midodrine
Intervention Type
Drug
Intervention Name(s)
Albumin
Intervention Description
Human albumin will be administered by intravenous infusion at a dose of 1.5 gm/kg/week for 2 weeks followed by HA 40 grams every 7days
Intervention Type
Drug
Intervention Name(s)
Midodrine
Intervention Description
Oral Midodrine will be given at a dose of 7.5 mg three times in a day
Intervention Type
Drug
Intervention Name(s)
Standard medical therapy (SMT)
Intervention Description
SMT will include nutritional support, rifaximin, lactulose or lactitol, diuretics, SBP prophylaxis with norfloxacin, restriction of sodium, multivitamins, and other supportive measures as deemed necessary. LVP will be done as needed. Patients on non-selective beta blockers will continue to do so with dose modifications/withdrawal as per Baveno VI guidelines.
Primary Outcome Measure Information:
Title
Number of patients with control of ascites at 1 year
Description
Control of ascites will be defined as-
Complete response will be total absence of ascites.
Partial response as presence of ascites not requiring paracentesis
Non response will be defined as persistence of severe ascites requiring paracentesis.
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Change in estimated glomerular filtration rate (eGFR) measured by modified diet in renal disease 6 (MDRD6) formula at 3 months intervals
Description
eGFR will be measured using MDRD6 formula
Time Frame
1 year
Title
Changes in concentration of albumin at 3 months intervals
Description
Change in concentration of serum albumin (g/dl)
Time Frame
1 year
Title
Change in model for end stage liver disease (MELD) score
Description
Change in MELD score. The MELD score incorporates the variables of serum bilirubin, creatinine and Internation Normalised Ratio (INR). Higher MELD score indicates worse prognosis
Time Frame
1 year
Title
Change in mean arterial pressure at 3 months interval
Description
Change in mean arterial pressure (mm of Hg) will be noted
Time Frame
1 year
Title
Changes in serum and 24- hour urine sodium
Description
Serum and urine sodium concentration will be measured in meq/L
Time Frame
1 year
Title
Incidence of spontaneous bacterial peritonitis (SBP) and other infections
Description
The diagnosis of SBP will be based on neutrophil count in ascitic fluid of >250/mm3 as determined by microscopy and positive ascitic fluid culture or >250 /mm3 with negative culture called as culture negative neutrocytic ascites.20 Other infections will be diagnosed as per CDC criteria.
Time Frame
1 year
Title
Number of patients who develop paracentesis induced circulatory dysfunction (PICD)
Description
PICD will be defined as an increase in plasma renin activity (PRA) of >50% of the pre-treatment value to a level > 4ng/ml/hr on 6th day after paracentesis
Time Frame
1 year
Title
Number of patients who develop hyponatremia
Description
Hyponatremia will be defined using serum sodium concentrations of <130meq/L.
Time Frame
1 year
Title
Change in Child-Turcotte-Pugh (CTP) score
Description
Change in CTP score. The CTP score incorporates the variables of serum bilirubin, albumin, prothrombin time-INR, grade of ascites and hepatic encephalopathy. The score ranges from 5-15 and a higher score portends a worse prognosis
Time Frame
1 year
Title
Number of patients who develop hypokalemia
Description
Hypokalemia will be defined using serum potassium levels <3 meq/L
Time Frame
1 year
Title
Number of patients who develop hyperkalemia
Description
hyperkalemia will be defined using serum potassium levels >6 meq/L
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age between 18 and 80 years
Refractory ascites in cirrhosis of any etiology
Exclusion Criteria:
Mixed ascites: cirrhosis plus another cause of ascites
Gastrointestinal bleed within 7 days of enrolment.
Presence of hepatorenal syndrome
Hepatic encephalopathy grade 2 or higher
Infection within 1 month preceding the study
Cardiovascular disease (ejection fraction < 35% or abnormal ECG) or arterial hypertension (BP > 140/90 mm of Hg)
Abnormal urine analysis with proteinuria > 500 mg/24 hour or 50 red blood cells/high power field, or granular casts or ultrasonographic evidence of intrinsic renal disease
Presence of hepatocellular carcinoma or portal vein thrombosis
Treatment with drug with known effects on systemic and renal hemodynamics within 7 days of inclusion excepting beta-blockers
Patient not willing for study.
Patient opting for liver transplantation/ transjugular intrahepatic portosystemic shunt
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Virendra Singh, MD, DM
Phone
0172-275-6338
Email
virendrasingh100@hotmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Amandeep Singh, MD
Phone
9815252928
Email
amandeep48@yahoo.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Virendra Singh, MD, DM
Organizational Affiliation
PGIMER, Chandigarh
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
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Midodrine and Albumin in Patients With Refractory Ascites
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