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Safety and Efficacy of Midodrine Hydrochloride in the Management of Refractory Ascites Due to Cirrhosis in Children

Primary Purpose

Refractory Ascites, Children, Only

Status
Unknown status
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
Midodrine 2.5 mg tab
Sponsored by
National Liver Institute, Egypt
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Refractory Ascites

Eligibility Criteria

7 Years - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Children aged 7-18 years
  • Both sexes
  • Having refractory ascites (not responding to maximal dose of diuretics
  • Diuretic-induced complications necessitate discontinuation of the drug

Exclusion Criteria:

  • Non-cirrhotic causes of ascites
  • Intrinsic renal disease ( e.g; polycystic kidney disease)
  • Active gastrointestinal bleeding or the presence of risky varices
  • Patients with Portal vein thrombosis and Budd-Chiari
  • Cardiovascular disease
  • Systemic hypertension or prehypertension
  • Hyperthyroidism
  • Patients with narrow-angle glucoma

Sites / Locations

  • Pediatric Hepatology, Gastroenterology and Nutrition Department, National Liver Institute, Menoufia UniversityRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Midodrine daily

Arm Description

Midodrine hydrochloride 2.5 mg tab once per day

Outcomes

Primary Outcome Measures

Side effect no 1
number of patients with Elevated BP: ≥90th percentile to <95th percentile
Side effect no 2
number of patients with Stage 1 HTN: ≥95th percentile to <95th percentile + 12 mmHg or 130/80 to 139/89 mm Hg (whichever is lower)
Side effect no 3
number of patients with Stage 2 HTN: ≥95th percentile + 12 mm Hg or ≥140/90 mm Hg (whichever is lower) mmHg or 130/80 to 139/89 mm Hg (whichever is lower)
Side effect no 4
number of patients with low heart rate
Side effect no 5
number of patients with urine retention
Side effect no 6
number of patients with severe itching
Side effect no 7
number of patients with skin rash

Secondary Outcome Measures

Complete Response
absence of ascites by abdominal ultrasound
Partial response
ascites cannot be mobilized completely but not symptomatic or needs paracentesis
non-response
no decrease in ascites which still in need for paracentesis after 3 months of duration

Full Information

First Posted
August 1, 2019
Last Updated
August 20, 2020
Sponsor
National Liver Institute, Egypt
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1. Study Identification

Unique Protocol Identification Number
NCT04043858
Brief Title
Safety and Efficacy of Midodrine Hydrochloride in the Management of Refractory Ascites Due to Cirrhosis in Children
Official Title
Safety and Efficacy of Midodrine Hydrochloride in the Management of Refractory Ascites Due to Cirrhosis in Children: a Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
August 2020
Overall Recruitment Status
Unknown status
Study Start Date
June 5, 2020 (Actual)
Primary Completion Date
June 5, 2021 (Anticipated)
Study Completion Date
December 1, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Liver Institute, Egypt

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Ascites in liver cirrhosis is explained by increased production of vasoactive substances leading to renal vasoconstriction and salt and water retention. The retained water then accumulates in the peritoneal cavity under the effect of portal hypertension and low albumin. Refractory ascites is defined as ascites that cannot be mobilized or prevented from early recurrence after large-volume paracentesis despite medical therapy and dietary sodium restriction. Midodrine is an α1 receptor agonist that can improve systemic and renal hemodynamics in non-azotemic cirrhotic patients by counteracting mesenteric vasodilatation, which is accentuated in cirrhosis.
Detailed Description
Ascites in liver cirrhosis is explained by increased production of vasoactive substances, such as nitric oxide, carbon monoxide, and endocannabinoids, which cause splanchnic vasodilatation, increased blood flow through this area, and a decrease in peripheral vascular resistance and the effective arterial volume with resulting reduction in renal blood flow with subsequent activation of rennin-angiotensin-aldosterone system which in turn leads to renal vasoconstriction and salt and water retention. The retained water then accumulates in the peritoneal cavity under the effect of portal hypertension and low albumin. The International Ascites Club defines refractory ascites as ascites that cannot be mobilized or prevented from early recurrence after large-volume paracentesis despite medical therapy and dietary sodium restriction. There are two varieties of refractory ascites: diuretic-resistant ascites that is unresponsive to the maximal tolerable dose of diuretic therapy and diuretic-intractable ascites when complications such as hepatic encephalopathy, renal dysfunction, or electrolyte abnormalities limit the use of diuretics in the effective therapeutic dose (Cárdenas and Arroyo, 2005) The therapeutic options for refractory ascites are serial therapeutic paracentesis, transjugular intrahepatic portosystemic shunt, peritoneovenous shunt, and liver transplantation. Midodrine is transformed into the active metabolite desglymidodrine, which is an α1 receptor agonist causing an increase in vascular tone and increase in blood pressure without β-adrenergic receptors stimulation so, it can improve systemic and renal hemodynamics in non-azotemic cirrhotic patients by counteracting mesenteric vasodilatation, which is accentuated in cirrhosis. It diffuses poorly across the blood-brain barrier with no central effects. In a study included 600 adult patients with refractory ascites, midodrine was added to diuretic therapy and lead to enhancement of diuresis with the improvement of systemic, renal hemodynamics and short-term survival. Approximately, the only use of midodrine hydrochloride in children was in postural orthostatic tachycardia syndrome (POTS) which showed a good efficacy and safety profile.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Refractory Ascites, Children, Only

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Midodrine daily
Arm Type
Experimental
Arm Description
Midodrine hydrochloride 2.5 mg tab once per day
Intervention Type
Drug
Intervention Name(s)
Midodrine 2.5 mg tab
Other Intervention Name(s)
ProAmatine
Intervention Description
Patients receive an oral daily dose of 2.5 mg midodrine if age 7-12 years and receive 2.5 mg twice daily of more than 12 years
Primary Outcome Measure Information:
Title
Side effect no 1
Description
number of patients with Elevated BP: ≥90th percentile to <95th percentile
Time Frame
3 months
Title
Side effect no 2
Description
number of patients with Stage 1 HTN: ≥95th percentile to <95th percentile + 12 mmHg or 130/80 to 139/89 mm Hg (whichever is lower)
Time Frame
3 months
Title
Side effect no 3
Description
number of patients with Stage 2 HTN: ≥95th percentile + 12 mm Hg or ≥140/90 mm Hg (whichever is lower) mmHg or 130/80 to 139/89 mm Hg (whichever is lower)
Time Frame
3 months
Title
Side effect no 4
Description
number of patients with low heart rate
Time Frame
3 months
Title
Side effect no 5
Description
number of patients with urine retention
Time Frame
3 months
Title
Side effect no 6
Description
number of patients with severe itching
Time Frame
3 months
Title
Side effect no 7
Description
number of patients with skin rash
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Complete Response
Description
absence of ascites by abdominal ultrasound
Time Frame
12 months
Title
Partial response
Description
ascites cannot be mobilized completely but not symptomatic or needs paracentesis
Time Frame
12 months
Title
non-response
Description
no decrease in ascites which still in need for paracentesis after 3 months of duration
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
7 Years
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Children aged 7-18 years Both sexes Having refractory ascites (not responding to maximal dose of diuretics Diuretic-induced complications necessitate discontinuation of the drug Exclusion Criteria: Non-cirrhotic causes of ascites Intrinsic renal disease ( e.g; polycystic kidney disease) Active gastrointestinal bleeding or the presence of risky varices Patients with Portal vein thrombosis and Budd-Chiari Cardiovascular disease Systemic hypertension or prehypertension Hyperthyroidism Patients with narrow-angle glucoma
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Bassam Ayoub, MD
Phone
+201000936418
Email
bassamayob@yahoo.com
First Name & Middle Initial & Last Name or Official Title & Degree
Mohamed Abdel Hafeez, MD
Phone
+201002362768
Email
abdelhafeez64@yahoo.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bassam Ayoub, MD
Organizational Affiliation
Pediatric Hepatology Dep; National Liver Institute, Menoufia University, Egypt
Official's Role
Principal Investigator
Facility Information:
Facility Name
Pediatric Hepatology, Gastroenterology and Nutrition Department, National Liver Institute, Menoufia University
City
Shibīn Al Kawm
State/Province
Menofiya
ZIP/Postal Code
32511
Country
Egypt
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bassam Ayoub, MD
Phone
+201000936418
Email
bassamayob@yahoo.com
First Name & Middle Initial & Last Name & Degree
Mohamed Abdel Hafeez, MD
Phone
+201002362768
Email
abdelhafeez64@yahoo.com
First Name & Middle Initial & Last Name & Degree
Tahany A Salem, MD
First Name & Middle Initial & Last Name & Degree
Marwa S Rizk, MD
First Name & Middle Initial & Last Name & Degree
Salma A Nage, MD
First Name & Middle Initial & Last Name & Degree
Rasha A Ali, MD

12. IPD Sharing Statement

Citations:
PubMed Identifier
16139922
Citation
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Results Reference
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PubMed Identifier
28895701
Citation
Bes DF, Cristina Fernandez M, Malla I, Repetto HA, Buamscha D, Lopez S, Martinitto R, Cuarterolo M, Alvarez F. Management of cirrhotic ascites in children: Review and recommendations. Part 2: Electrolyte disturbances, nonelectrolyte disturbances, therapeutic options. Arch Argent Pediatr. 2017 Oct 1;115(5):505-511. doi: 10.5546/aap.2017.eng.505. English, Spanish.
Results Reference
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PubMed Identifier
15920323
Citation
Cardenas A, Arroyo V. Refractory ascites. Dig Dis. 2005;23(1):30-8. doi: 10.1159/000084723.
Results Reference
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PubMed Identifier
21301135
Citation
Chen L, Wang L, Sun J, Qin J, Tang C, Jin H, Du J. Midodrine hydrochloride is effective in the treatment of children with postural orthostatic tachycardia syndrome. Circ J. 2011;75(4):927-31. doi: 10.1253/circj.cj-10-0514. Epub 2011 Feb 2.
Results Reference
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PubMed Identifier
29035421
Citation
Dionne JM. Updated Guideline May Improve the Recognition and Diagnosis of Hypertension in Children and Adolescents; Review of the 2017 AAP Blood Pressure Clinical Practice Guideline. Curr Hypertens Rep. 2017 Oct 16;19(10):84. doi: 10.1007/s11906-017-0780-8.
Results Reference
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PubMed Identifier
24369273
Citation
JCS Joint Working Group. Guidelines for drug therapy in pediatric patients with cardiovascular diseases (JCS 2012). Digest version. Circ J. 2014;78(2):507-33. doi: 10.1253/circj.cj-66-0083. Epub 2013 Dec 26. No abstract available.
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PubMed Identifier
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Citation
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Results Reference
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PubMed Identifier
30126937
Citation
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Results Reference
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Citation
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Results Reference
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Safety and Efficacy of Midodrine Hydrochloride in the Management of Refractory Ascites Due to Cirrhosis in Children

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