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High Versus Low Dose of Caffeine for Apnea of Prematurity

Primary Purpose

Apnea, Preterm Infants

Status
Completed
Phase
Phase 3
Locations
Egypt
Study Type
Interventional
Intervention
Caffeine citrate
Sponsored by
Mansoura University Children Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Apnea focused on measuring high dose of caffeine, low dose of caffeine, prevention

Eligibility Criteria

1 Day - 10 Days (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • newborn infant less than 32 weeks gestation with the diagnosis of apnea

Exclusion Criteria:

  • newborn infants with gestational age more than 32 weeks.
  • newborn infant with congenital malformations or chromosomal anomalies.

Sites / Locations

  • Mansoura University Children Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

High dose caffeine

Low dose caffeine

Arm Description

High dose (loading 40 mg/kg/day equivalent to 20 mg /kg/day of caffeine base and maintenance of 20 mg/kg/day equivalent to 10 mg /kg/day of caffeine base)

Low dose (loading 20 mg/kg/day equivalent to 10 mg /kg/day of caffeine base and maintenance of 10 mg/kg/day equivalent to 5 mg /kg/day of caffeine base) caffeine.

Outcomes

Primary Outcome Measures

Successful extubation from mechanical ventilation
Need of re-intubation within 72 hours of extubation from mechanical ventilation

Secondary Outcome Measures

Apnea of prematurity
Frequency and documented days of apnea
Duration of mechanical ventilation and oxygen support
length of hospital stay
Neonatal mortality
Death before hospital discharge
Chronic lung disease
Need for oxygen by 36 weeks corrected gestational age
Necrotising enterocolitis
Intraventricular haemorrhage
Periventricular leukomalacia
Hydrocephalus
Retinopathy of prematurity
Caffeine side effects.

Full Information

First Posted
March 27, 2014
Last Updated
April 3, 2014
Sponsor
Mansoura University Children Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02103777
Brief Title
High Versus Low Dose of Caffeine for Apnea of Prematurity
Official Title
High Versus Low Dose of Caffeine for Apnea of Prematurity: A Double Blind Randomized Control Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2014
Overall Recruitment Status
Completed
Study Start Date
September 2011 (undefined)
Primary Completion Date
September 2013 (Actual)
Study Completion Date
September 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mansoura University Children Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The optimum caffeine dose for apnea of prematurity has not been well investigated so the objective of the study is to compare high versus low dose of caffeine citrate to facilitate successful extubation in mechanically ventilated preterm infants.
Detailed Description
A randomized, double blind, clinical trial which will be conducted in Neonatal Intensive Care Unit, Mansoura University Children Hospital, Egypt on preterm infants born less than 32 weeks gestation mechanically ventilated within the first 10 days of life to study the optimum caffeine dose for apnea of prematurity and compare High dose (loading 40 mg/kg/day equivalent to 20 mg /kg/day of caffeine base and maintenance of 20 mg/kg/day equivalent to 10 mg /kg/day of caffeine base) versus low dose (loading 20 mg/kg/day equivalent to 10 mg /kg/day of caffeine base and maintenance of 10 mg/kg/day equivalent to 5 mg /kg/day of caffeine base) caffeine citrate started within the first 10 days of life and its effect on need of re-intubation within 72 hours of extubation from mechanical ventilation as primary outcome and frequency and duration of apnea, duration of mechanical ventilation and oxygen support, length of hospital stay, neonatal mortality, chronic lung disease, necrotising enterocolitis, intraventricular haemorrhage, periventricular leukomalacia, hydrocephalus, retinopathy of prematurity, and caffeine side effects as secondary outcomes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Apnea, Preterm Infants
Keywords
high dose of caffeine, low dose of caffeine, prevention

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
120 (Actual)

8. Arms, Groups, and Interventions

Arm Title
High dose caffeine
Arm Type
Active Comparator
Arm Description
High dose (loading 40 mg/kg/day equivalent to 20 mg /kg/day of caffeine base and maintenance of 20 mg/kg/day equivalent to 10 mg /kg/day of caffeine base)
Arm Title
Low dose caffeine
Arm Type
Active Comparator
Arm Description
Low dose (loading 20 mg/kg/day equivalent to 10 mg /kg/day of caffeine base and maintenance of 10 mg/kg/day equivalent to 5 mg /kg/day of caffeine base) caffeine.
Intervention Type
Drug
Intervention Name(s)
Caffeine citrate
Intervention Description
Caffeine will be given by either high dose in Arm 1 or low dose in Arm 2
Primary Outcome Measure Information:
Title
Successful extubation from mechanical ventilation
Description
Need of re-intubation within 72 hours of extubation from mechanical ventilation
Time Frame
72 hours after extubation from mechanical ventilation
Secondary Outcome Measure Information:
Title
Apnea of prematurity
Description
Frequency and documented days of apnea
Time Frame
Expected average of 8 weeks post natal age
Title
Duration of mechanical ventilation and oxygen support
Time Frame
Expected 4 to 6 weeks postnatal age
Title
length of hospital stay
Time Frame
Expected 8 weeks
Title
Neonatal mortality
Description
Death before hospital discharge
Time Frame
Expected 8 weeks
Title
Chronic lung disease
Description
Need for oxygen by 36 weeks corrected gestational age
Time Frame
By 36 weeks corrected gestational age
Title
Necrotising enterocolitis
Time Frame
Expected 6 weeks
Title
Intraventricular haemorrhage
Time Frame
Expected 2 weeks
Title
Periventricular leukomalacia
Time Frame
Expected 8 weeks
Title
Hydrocephalus
Time Frame
Expected 8 weeks
Title
Retinopathy of prematurity
Time Frame
Expected 8 weeks
Title
Caffeine side effects.
Time Frame
Expected 6 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Day
Maximum Age & Unit of Time
10 Days
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: newborn infant less than 32 weeks gestation with the diagnosis of apnea Exclusion Criteria: newborn infants with gestational age more than 32 weeks. newborn infant with congenital malformations or chromosomal anomalies.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
sameh m abbas, master
Organizational Affiliation
Mansoura University Children Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
nehad a nasef, MD
Organizational Affiliation
Mansoura University Children Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Mansoura University Children Hospital
City
Mansoura
State/Province
El Dakahlya
ZIP/Postal Code
35111
Country
Egypt

12. IPD Sharing Statement

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High Versus Low Dose of Caffeine for Apnea of Prematurity

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