Comparison of Continuous Positive Airway Pressure and Non Invasive Positive Pressure Ventilation

NCT ID: NCT03347136

Last Updated: 2017-11-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

80 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-01-10

Study Completion Date

2015-12-28

Brief Summary

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The objective of the study is to compare the effectiveness of treatment with Non Invasive Positive Pressure Ventilation (NIPPV) and continuous positive airway pressure (CPAP) in decreasing the requirement for endotracheal ventilation in neonates with respiratory distress within the first hours of birth.Primary outcome is the non invasive respiratory support failure and the need for intubated ventilatory support during the first 72 hours of life.

Randomized control , single center trial. Eighty neonates admitted to Neonatal Intensive Care Unit (NICU) were randomly allocated to NIPPV and CPAP. Outcomes of respiratory support were observed and information on risk factors were obtained by going through bed head ticket.

Detailed Description

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Objective of the study:

To compare the effectiveness of CPAP and NIPPV in neonates with mild to moderate respiratory distress.

Specific objectives To determine the effectiveness of CPAP and NIPPV in neonates with mild to moderate respiratory distress To describe neonatal factors associated with CPAP and NIPPV support. To compare the length of hospital stay in neonates who received CPAP and NIPPV To compare the time taken to achieve full enteral nutrition in neonates who received CPAP and NIPPV.

Study design:

Randomized controlled trial

Study setting:

Study carried out in NICU of the Sri Jayawardanapura General Hospital There are 06 ventilators in NICU of Sri Jayawardanapura Hospital. (Three SLE 2000 infant ventilators and three Bear CUB 750 psv infant ventilators.) Respiratory support (conventional ventilation, CPAP and NIPPV) gave through these ventilators. The neonatal soft tip curved nasal canula with tubing will be use for non invasive respiratory support. The nasal canula connected to the ventilator via an endotracheal tube connector. Systems were regularly monitored. Canula size was chosen to comfortably fit the infant's nostrils.

CPAP started with Positive end expiratory pressure (PEEP) 05 and increased up to PEEP 09 according to the severity of baby's condition.

NIPPV started with intermittent Mandatory ventilation (IMV) rate 30, peak inspiratory pressure (PIP) 20 and PEEP 5.Increased the settings according to the severity of baby's condition.

Sampling Method. All neonates fulfilling inclusion and exclusion criteria registered in the study. And a serial number issued. They were allocated to the two arms of study randomly based on a previously generated random allocation schedule.

They were managed according to hospital management protocol and outcome data were collected from the bed head ticket.

The ethical approval taken from the Ethical Review Committee of Sri Jayawardenepura General Hospital kotte.

Approval taken from Medical Technology and supplies sub committee on clinical trials Written informed consent obtained from parents or guardians of eligible infants before randomization The data sheets did not contain the name and be anonymous. Data stored under lock and key with restricted access only to the principal investigators. The computerized data were password protected and is only available to the investigators.

Conditions

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Respiratory Distress of Newborn

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

The neonates with mild to moderate respiratory distress were randomly allocated to tratment with NIPPV and CPAP.
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Due to type of intervention masking was not possible.

Study Groups

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Newborns with CPAP support

Newborn with mild to moderate respiratory distress randomly allocated to CPAP arm. CPAP started with Positive End Expiatory Pressure(PEEEP) 05 and increased up to PEEP 09 according to the severity of baby's condition.

Group Type ACTIVE_COMPARATOR

CPAP

Intervention Type DEVICE

Newborns with NIPPV support

Newborn with mild to moderate respiratory distress randomly allocated to NIPPV arm. NIPPV started with Intermittent Mandatory Ventilation rate 30, Peak Inspiratory Pressure 20 and PEEP 5.Increased the settings according to the severity of baby's condition

Group Type EXPERIMENTAL

NIPPV

Intervention Type DEVICE

Interventions

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CPAP

Intervention Type DEVICE

NIPPV

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

All neonates with mild to moderate respiratory distress, requiring non invasive respiratory support on admission as defined by one or more of the following

1. Respiratory distress needing 3L of O2 to maintain saturation of \>90%
2. Silverman Anderson score of 4 - 6
3. Apnoea

1. \>2 apnoeic attacks needing tactile stimulation for recovery.
2. One apnoea needs resuscitation

Exclusion Criteria

1. Major congenital anomalies
2. Presence of cardiovascular instability {sepsis, anemia or severe intraventricular haemorrhage (IVH)}.
3. Intubation needed on admission to the NICU
4. Consent not provided or refused
5. Major cardiac disease (not including patent ductus arteriosus \[PDA\]),

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Minimum Eligible Age

20 Minutes

Maximum Eligible Age

24 Hours

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Ministry of Health, Sri Lanka

OTHER_GOV

Sponsor Role lead

Responsible Party

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Dr. Anne kaushalya Shilani Gomez,MBBS,MD

acting consultant neonatologist

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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ANNE KS GOMEZ, MBBS,MD

Role: PRINCIPAL_INVESTIGATOR

Teaching Hospital Mahamodara

Locations

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Sri Jayawardanapura teaching hospital

Colombo, Western Province, Sri Lanka

Site Status

Countries

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Sri Lanka

References

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DK Guha, editors, Jaypee Brothers. NNF Recommended Basic Perinatal-Neonatal Nomenclature. Neonatology- Principles and Practice. 1st ed. New Delhi, 1998: 131-2

Reference Type BACKGROUND

J Crowther ANNP Updated by Dr Smith. East Cheshire NHS trust Endotracheal Intubation guide line February 2013 Version 2.0 3

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Perinatal society of Sri Lanka in collaborating with WHO collaborating centre for training and research in new born care, All India Institute of Medical Science.Work book on neonatal ventilation.Learner's guide April 2008.

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Khalaf MN, Brodsky N, Hurley J, Bhandari V. A prospective randomized, controlled trial comparing synchronized nasal intermittent positive pressure ventilation versus nasal continuous positive airway pressure as modes of extubation. Pediatrics. 2001 Jul;108(1):13-7. doi: 10.1542/peds.108.1.13.

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Reference Type RESULT
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Reference Type RESULT
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Reference Type RESULT
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Reference Type RESULT
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Reference Type RESULT
PMID: 17804519 (View on PubMed)

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Reference Type RESULT
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Reference Type RESULT
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Reference Type RESULT
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Reference Type RESULT

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Reference Type RESULT
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Reference Type RESULT
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Related Links

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https://www.uptodate.com

Mechanical ventilation in neonates.Version 19.3

Other Identifiers

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MOHSriLanka

Identifier Type: -

Identifier Source: org_study_id