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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
Postgraduate Institute of Medical Education and Research
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Refractory Ascites

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age between 18 and 80 years
  2. Refractory ascites in cirrhosis of any etiology

Exclusion Criteria:

  1. Mixed ascites: cirrhosis plus another cause of ascites
  2. Gastrointestinal bleed within 7 days of enrolment.
  3. Presence of hepatorenal syndrome
  4. Hepatic encephalopathy grade 2 or higher
  5. Infection within 1 month preceding the study
  6. Cardiovascular disease (ejection fraction < 35% or abnormal ECG) or arterial hypertension (BP > 140/90 mm of Hg)
  7. 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
  8. Presence of hepatocellular carcinoma or portal vein thrombosis
  9. Treatment with drug with known effects on systemic and renal hemodynamics within 7 days of inclusion excepting beta-blockers
  10. Patient not willing for study.
  11. 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

    First Posted
    October 27, 2020
    Last Updated
    November 3, 2020
    Sponsor
    Postgraduate Institute of Medical Education and Research
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    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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