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Sildenofil in Persistent Pulmonary Hypertension in Newborns (Sildeno)

Primary Purpose

Persistent Fetal Circulation Syndrome

Status
Unknown status
Phase
Phase 3
Locations
Qatar
Study Type
Interventional
Intervention
Sildenafil
diluent
Sponsored by
Hamad Medical Corporation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Persistent Fetal Circulation Syndrome focused on measuring newborn, INO, Sildenafil, PPHN

Eligibility Criteria

36 Weeks - 41 Weeks (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Newborn infants of post natal age less than 48 hours
  2. Gestational age equal to or more than 34 weeks
  3. Oxygen index of more than or equal to 20 (moderately ill infants)
  4. Radiological, clinical and biochemical evidence of acute hypoxic respiratory failure
  5. Surfactant therapy has been established when indicated
  6. Presence of arterial line

Exclusion Criteria:

  1. Congenital diaphragmatic hernia
  2. Major congenital abnormalities
  3. Significant congenital heart disease
  4. Cyanotic congenital heart disease

Sites / Locations

  • Women's hospital, NICURecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Active Comparator

Arm Label

Group A - Placebo

Group B- Sildenafil

Arm Description

iNO combined with placebo will be administered

iNO combined with Sildenafil

Outcomes

Primary Outcome Measures

Oxygen index
OI= PaO2 X FiO2/100( Absolute values and change from baseline measurement after first dose, measured every 6 hours for 7 days while on therapy. Improvement in OI is defined as decrease in OI of 20% from the previously calculated value.
A-a gradient
Alveolar arterial oxygen difference gradient
Hemodynamic parameters
Hemodynamic parameters ( absolute values and change from baseline measured after the first dose, after 24 hours, after 36 hours, and after 48 hours and every 12 hours thereafter for a total of 7 days while receiving therapy and 7 days after the end of treatment including : 1. Heart rate, mean blood pressure, respiratory rate, oxygen saturation and blood gas b. Pulmonary arterial pressure in mm Hg measured by echocardiography c. cArdiac output in liter/kg/min d. Oxygenation ( PaO2) and FiO2 requirement

Secondary Outcome Measures

Days of hospitalization
Length of hospitalization and mortality, morbidity, ventialtion dats , adverse events
mortality
All cause mortality within 28 days of life

Full Information

First Posted
March 11, 2012
Last Updated
September 23, 2012
Sponsor
Hamad Medical Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT01558466
Brief Title
Sildenofil in Persistent Pulmonary Hypertension in Newborns
Acronym
Sildeno
Official Title
Early Combined Use of Inhaled Nitric Oxide and Oral Sildenafil on the Outcome of Pulmonary Hypertension in New Born Infants
Study Type
Interventional

2. Study Status

Record Verification Date
September 2012
Overall Recruitment Status
Unknown status
Study Start Date
November 2011 (undefined)
Primary Completion Date
November 2014 (Anticipated)
Study Completion Date
June 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hamad Medical Corporation

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study hopes to evaluate the effectiveness of early combined use of Sildenafil and nitric oxide (iNO) in newborns with Persistent pulmonary hypertension (PPHN) and or hypoxemic respiratory failure and assess whether this would improve oxygenation, improve time on mechanical ventilation for these babies and also prevent rebound hypoxic episodes.
Detailed Description
PPHN is characterized by hyper reactivity of the muscle layer in pulmonary arterioles and right to left shunt across the ductus arteriosus and the foramen ovale in the absence of structural heart defects. It could also include right ventricle dysfunction in many cases. The reported incidence of this disease is 0.43 to 6.8/1000 live new born infants with a mortality of 10-20%. The main objective of therapy in PPHN is to reduce pulmonary vascular resistance. To this purpose, inhaled nitric oxide has been used in developed and several under developed countries. However 30-40% of these patients do not respond to this therapy. Extra corporeal membrane oxygenation is also useful but is an invasive therapy in PPHN with serious adverse effects reported. Recently Sildenafil has been evaluated as an alternative or adjunctive pulmonary vasodilator. It inhibits phosphodiesterase type 5 and elevates the concentration of cyclic guanosine monophosphate in the muscle cells of pulmonary vessels, which in turn decreases pulmonary vascular resistance. The FDA in the USA has recently approved the use of Sildenafil for use in adults with PPHN. Recently 3 clinical trials have evaluated Sildenafil versus Placebo or control in newborns with PPHN,all of them showing a significant improvement in oxygenation index, decreased mortality and reduced risk of rebounds after discontinuing iNO. The use of Sildenafil in treating PPHN secondary to Chronic lung disease in older infants had been receiving significant attention over the last few years. At HMC, Women's hospital, the number of deliveries average 15,000 to 16,000 per year with an admission rate to the NICU of about 10%. The number of PPHN cases admitted to our NICU ranges between 14-20 cases per year. In this study the investigators plan to compare the effectiveness of the use of early combined Sildenafil and iNO in newborns with PPHN and or hypoxemic respiratory failure and whether it would improve oxygenation, decrease the time spent in mechanical ventilation and prevent rebound hypoxic episodes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Persistent Fetal Circulation Syndrome
Keywords
newborn, INO, Sildenafil, PPHN

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Group A - Placebo
Arm Type
Placebo Comparator
Arm Description
iNO combined with placebo will be administered
Arm Title
Group B- Sildenafil
Arm Type
Active Comparator
Arm Description
iNO combined with Sildenafil
Intervention Type
Drug
Intervention Name(s)
Sildenafil
Other Intervention Name(s)
Viagra
Intervention Description
50 mg tablet will be thoroughly crushed into powder form and diluted in 10 ml ora base suspension syrup agent and a dilution will be performed to prepare 5 mg/ml. All doses required for 48 hours will be available; solutions will be stored at 2-8 degrees C where solution should be stable for at least a month.
Intervention Type
Drug
Intervention Name(s)
diluent
Other Intervention Name(s)
Normal saline
Intervention Description
The placebo will have an equal volume of diluent - Orabase syrup of the same colour and viscosity as the active comparator. Infants in this group will receive normal saline as placebo every 6 hours
Primary Outcome Measure Information:
Title
Oxygen index
Description
OI= PaO2 X FiO2/100( Absolute values and change from baseline measurement after first dose, measured every 6 hours for 7 days while on therapy. Improvement in OI is defined as decrease in OI of 20% from the previously calculated value.
Time Frame
7 days after birth and admission to the NICU
Title
A-a gradient
Description
Alveolar arterial oxygen difference gradient
Time Frame
7 days after admission to the NICU
Title
Hemodynamic parameters
Description
Hemodynamic parameters ( absolute values and change from baseline measured after the first dose, after 24 hours, after 36 hours, and after 48 hours and every 12 hours thereafter for a total of 7 days while receiving therapy and 7 days after the end of treatment including : 1. Heart rate, mean blood pressure, respiratory rate, oxygen saturation and blood gas b. Pulmonary arterial pressure in mm Hg measured by echocardiography c. cArdiac output in liter/kg/min d. Oxygenation ( PaO2) and FiO2 requirement
Time Frame
7 days
Secondary Outcome Measure Information:
Title
Days of hospitalization
Description
Length of hospitalization and mortality, morbidity, ventialtion dats , adverse events
Time Frame
7 days after admission to the NICU
Title
mortality
Description
All cause mortality within 28 days of life
Time Frame
28 days of life

10. Eligibility

Sex
All
Minimum Age & Unit of Time
36 Weeks
Maximum Age & Unit of Time
41 Weeks
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Newborn infants of post natal age less than 48 hours Gestational age equal to or more than 34 weeks Oxygen index of more than or equal to 20 (moderately ill infants) Radiological, clinical and biochemical evidence of acute hypoxic respiratory failure Surfactant therapy has been established when indicated Presence of arterial line Exclusion Criteria: Congenital diaphragmatic hernia Major congenital abnormalities Significant congenital heart disease Cyanotic congenital heart disease
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Husam Em Salama, MRCP
Phone
00974- 55262159
Email
hsalama1@hmc.org.qa
First Name & Middle Initial & Last Name or Official Title & Degree
Ahmed Masoud, MD
Phone
00974-55112369
Email
amasoud@hmc.org.qa
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Husam Salama, MD
Organizational Affiliation
Hamad Medical Corporation, Doha, Qatar
Official's Role
Principal Investigator
Facility Information:
Facility Name
Women's hospital, NICU
City
Doha
ZIP/Postal Code
00974
Country
Qatar
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Husam Salama, MD
Phone
552262159
Email
hsalama1@hmc.org.qa
First Name & Middle Initial & Last Name & Degree
Ahmad Masoud, MD
Phone
55112369
Email
amasoud@hmc.org.qa
First Name & Middle Initial & Last Name & Degree
Husam Salama, MD
First Name & Middle Initial & Last Name & Degree
Ahmad Masoud, MD
First Name & Middle Initial & Last Name & Degree
Moza Al Hail, BpH
First Name & Middle Initial & Last Name & Degree
Hilal Al Rifai, MD
First Name & Middle Initial & Last Name & Degree
Mohamed Bunaiha, BpH
First Name & Middle Initial & Last Name & Degree
Samawal Lutfi, MD
First Name & Middle Initial & Last Name & Degree
Mohamad Delawar, MD
First Name & Middle Initial & Last Name & Degree
Badr Kurdi, MD
First Name & Middle Initial & Last Name & Degree
Afif Ali, B.PH
First Name & Middle Initial & Last Name & Degree
Robert Hightree, RT
First Name & Middle Initial & Last Name & Degree
Ghassan Abdoh, MD
First Name & Middle Initial & Last Name & Degree
Samer Taha, Fellowship

12. IPD Sharing Statement

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Sildenofil in Persistent Pulmonary Hypertension in Newborns

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