Caffeine; Sleep DisorderNCT04376749
Influence of Caffeine Therapy in Preterm Infants
An observational study of Caffeine; Sleep Disorder, run by Marmara University at 1 site in Turkey (Türkiye).
Trial summary
The development of sleep wake cycles is indicative of child's neurocognitive functions. Caffeine therapy is commonly used in neonatal intensive care units for treatment of apnea of prematurity (AOP), to reduce mechanical ventilation, and improve the success of extubation. Read more about this study
- Who is it for?
- Ages 28 to 34 weeks
- Conditions the study is for
- Caffeine; Sleep Disorder
- How many people
- 40 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- May 2020to May 2021
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 28 to 34 weeks
- All sexes
- No healthy volunteers
- Child
Study population: Preterm infants born between 28 to 34 gestational weeks admitted to the Marmara University Neonatal Intensive Care Unit (NICU) during one year period
Who may be able to join
- Preterm infants born between 28 to 34 gestational weeks admitted to the Marmara University Neonatal Intensive Care Unit (NICU)
Who cannot join
- perinatal asphyxia intraventricular hemorrhage grade 3 or higher retinopathy of prematurity(ROP) of stage 3 or higher major congenital anomalies infants using sedative or anticonvulsant drugs at the time of data collection
Trial locations and contacts
1 site in 1 country.
Turkey (Türkiye)1 site
Marmara University School of Medicine
Istanbul
About this study
Official title: Influence of Caffeine Therapy in Preterm Infants on Sleep and Neurodevelopmental Outcomes During the First Year of Life: a Single Center Experience
The development of sleep wake cycles is indicative of child's neurocognitive functions. Caffeine therapy is commonly used in neonatal intensive care units for treatment of apnea of prematurity (AOP), to reduce mechanical ventilation, and improve the success of extubation. In addition, it is suggested to be associated with positive long-term outcomes on pulmonary function and neurodevelopment. However, it is still not clear how caffeine therapy affects the sleep architecture and neurodevelopment of preterm infants. Furthermore, optimal dosing and timing of caffeine therapy is controversial.
We aimed to evaluate the effects of caffeine therapy on sleep architecture and neurodevelopment in preterm infants during the first year of life.
Read more
A prospective observational case-control study will be conducted. Forty preterm infants aged between 28 to 34 gestational weeks admitted to the Marmara University Neonatal Intensive Care Unit (NICU) from May 2020 to May 2021 will be included. Infants with neonatal risk factors for poor neurodevelopmental outcomes will be excluded. Duration, timing and cumulative dosage of caffeine therapy will be calculated. Follow up outcome for neurodevelopment and sleep architecture of preterm infants who received caffeine therapy will be compared with those who did not receive caffeine therapy.
Sleep and activity behavior recorded by actigraphy, sleep diary and polysomnography at 6, and 12 months corrected age will be compared to noncaffeine group. Neurodevelopment will be assessed by neurological examination defined by Hammersmith, Ages and Stages Questionnaire (ASQ-2), and Bayley Scales of Infant and Toddler Development.
Read the detailed description
Methylxanthines have been prescribed in preterm infants to treat and prevent Apnea of Prematurity (AOP), for extubation success, for reduction of incidence of BPD, need for treatment of PDA, retinopathy of prematurity, IVH, and for neuroprotective effects. Caffeine is the most common drug of choice. Despite its frequent use there are no standardized protocols for optimal timing and dosage. It is suggested to have a neuroprotective effect, and associated with reduction of neurological disabilities, cognitive delay. However, there are studies which found no difference in poor neurological outcomes compared to control.
Premature infants have more active sleep compared to term infants, and their sleep patterns mature gradually. Studies about the effects of caffeine therapy on sleep of premature infants are few. It is known that sleep is associated with child's neurodevelopmental outcomes. Identifying the impact of caffeine therapy on sleep will help clinicians to identify and improve neurodevelopmental problems in this vulnerable study population.
The aim of this study is to evaluate the effects of caffeine therapy on sleep, activity patterns and neurodevelopment in preterm infants during the first year of life.
Based on the assumption that each year approximately 20 infants receive neonatal caffeine therapy in the unit, forty preterm infants aged between 28 to 34 gestational weeks admitted to the Marmara University Neonatal Intensive Care Unit (NICU) from May 2020 to May 2021 will be included. Duration, timing and cumulative dosage of caffeine therapy will be calculated. The routine practice of Marmara University NICU protocol is to administer caffeine prophylaxis to infants born at less than 30 weeks of gestational age and/or infants with less than 1250 grams gestational weight. Infants born between 30 to 34 weeks of gestational age who has AOP are treated with caffeine therapy with the commonly prescribed dose of 20 mg/kg loading, and 5-10 mg/kg/day maintenance. Neonatal caffeine therapy continues until the infants are 34 weeks corrected gestational age and free of any apnea episodes for at least 7 days. Infants with neonatal risk factors for poor neurodevelopmental outcomes such as infants with perinatal asphyxia, intraventricular hemorrhage grade 3 or higher, retinopathy of prematurity(ROP) of stage 3 or higher, infants using sedative or anticonvulsant drugs at the time of data collection will be excluded.
Follow up outcome for sleep architecture and neurodevelopment of preterm infants who received caffeine therapy will be compared with those who did not receive caffeine therapy.
Actigraphy Sleep and activity behavior recorded by sleep diary, actigraphy and polysomnography at 6, and 12 months corrected age will be compared to noncaffeine group. Sleep wake patterns will be assessed by Philips Respironics Mini-Mitter Actiwatch-2 for at least 3 days at home environment and sleep diaries within 5-minute intervals will be filled out by parents simultaneously. Actigraphy is a validated wristwatch-like device that distinguishes sleep from wakefulness based on accelerometer measured movement. The actiwatch weighs 16 grams and will be placed on the infant's left ankle. For actigraphy interpretation, if the activity count exceeds a predefined threshold value the epoch is scored as wake state. 10 minutes with no movements on autograph will be determined as sleep phase. High frequency movements with >40 movements in each epoch lasting >10 minutes will be determined as wake state. According to the frequency of infants' movements, a number of sleep-wake variables will be calculated for analyses with Philips Actiware 6.1.8 software. Mean total sleep duration, mean sleep duration during the day, mean sleep duration at night, sleep onset latency (SOL: time taken to fall asleep after reported lights out), wake after sleep onset (WASO: number of minutes recorded as wake between sleep onset and sleep offset), longest consolidated sleep period at night (midnight and 6 am), number of night waking, and sleep efficiency (TST/ time in bed, reported as percent) will be determined.
Polysomnography Infants will undergo 3-4 hours polysomnography (Embla Systems N7000) in the pediatric sleep laboratory. Further validation of the actigraphy will be performed by an epoch-by-epoch comparison of actigraphy and simultaneous polysomnography data. The following variables will be monitored: electroencephalography, electromyography, electrocardiography, heart rate and respiratory rate. Respiration will be monitored with a nasal-cannula- pressure transducer, thoracic and abdominal inductive plethysmography bands and pulse-oximetry. Polysomnography will be recorded with Embla RemLogic software. For polysomnography scoring, recommendations of the American Academy of Sleep Medicine Guidelines-2017 will be followed. The polysomnography data will be analyzed by an expert physician blinded to the actigraphy results or the newborn infant's clinical data, except for gestational age and days of life. Apnea-hypopnea index (AHI) will be determined.
Our secondary objective is to assess neurodevelopment of these infants. Neurodevelopment will be assessed by neurological examination defined by Hammersmith, Ages and Stages Questionnaire (ASQ), and Bayley Scales of Infant and Toddler Development at 6, and 12 months corrected age and will be compared to noncaffeine group.
Neurological examination will be performed with Hammersmith Neurological Examination. Hammersmith Neurological Examination is a quick examination for 3 to 24 months old infants. It consists of 26 items assessing neurological function in 5 groups: cranial nerve function (max 15 points), posture (maximum 18 points), movements (maximum 6 points), tone (maximum 24 points) and reflexes and reactions (maximum 15 points). Each subgroup is scored from 0 to 3 points and all scores are summed at the end of the examination.
Ages and Stages Questionnaire helps to evaluate developmental progress in children between the ages of 1 month and 66 months. Ages and Stages Questionnaire lasts approximately 10-15 minutes and assess the child development in 5 developmental areas: gross motor, fine motor, communication, problem solving and personal- social. Each area consists of 6 questions and the questions are answered in 3 simple responses: yes, sometimes or not yet. The questionnaire is scored with a simple 0, 5- and 10-point scoring system (yes: 10 points, sometimes: 5 points, not yet: 0 points) in 2-3 minutes by parents and the results are interpreted according to standardized cutoffs by professionals. Ages and Stages Questionnaire-2 (ASQ-2) is a parent-friendly developmental scale with 0.86 sensitivity, 0.85 specifity, 0.92 test-retest reliability and 0.93 inter-rater reliability. If the score on any domain is <2SDs below the cut-off point for the Turkish reference group, the child is defined as at risk for neurodevelopmental delay.
The Bayley Scales of Infant and Toddler Development, 3rd Edition produces three composite scores: the Cognitive Scale (range 55-145), the Language scale (range 45-155) which has receptive and expressive communication subtests, and the Motor scale (range 45-155), which consists of Fine Motor, and Gross Motor subtests.
Child's scores will be compared to the standardized age norms.
- Conditions
- Caffeine; Sleep Disorder
- Keywords
- caffeine,, sleep wake disorder, preterm, neurodevelopment, actigraphy
- Medical subject headings
- Sleep Wake Disorders, Premature Birth
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| preterm infants received caffeine | preterm infants aged between 28 to 34 weeks gestational age who received caffeine therapy either for prophylaxis or treatment | |
| preterm infants received no caffeine | preterm infants aged between 28 to 34 weeks gestational age who received no caffeine therapy |
What is being measured
The primary outcome is the main question the study is designed to answer.
Sleep and activity behavior
Sleep and activity behavior recorded by actigraphy
Measured: 6 months corrected age
Sleep and activity behavior
Sleep and activity behavior recorded by actigraphy
Measured: 12 months corrected age
Obstructive Apnea and Hypopnea Index
Obstrcutive Apnea and Hypopnea Index recorded by Polysomnography
Measured: 6 months corrected age
Obstructive Apnea and Hypopnea Index
Obstrcutive Apnea and Hypopnea Index recorded by Polysomnography
Measured: 12 months corrected age
Secondary outcomes (3)
Neurodevelopment
Neurological examination by Hammersmith
Measured: 6 and 12 months corrected age
Neurodevelopment
Neurodevelopment assessed by Ages and Stages Questionnaire (ASQ-2)
Measured: 6 and 12 months corrected age
Neurodevelopment
Neurodevelopment assessed by Bayley Scales of Infant and Toddler Development, 3rd edition
Measured: 6 and 12 months corrected age
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted6 May 2020
- Study startMay 2020 (estimated)
- Primary completionMay 2021 (estimated)
- Study completionMay 2021 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Caffeine; Sleep DisorderStudies of the same condition, open and under way.
- More trials run by Marmara UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Case-control
- Time perspective
- Prospective
- Enrolment
- 40 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Marmara University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Perran Boran, MD, PhD, Principal investigator, Marmara University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04376749
- Sponsor's protocol ID
- 09.2019.950
- Status last verified
- May 2020
- First submitted
- 3 May 2020
- Last updated
- 6 May 2020
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Atalah YEY, Baris HE, Akdere SK, Sabanci M, Ozdemir H, Gucuyener K, Eralp EE, Ozek E, Boran P. Effects of caffeine therapy for apnea of prematurity on sleep and neurodevelopment of preterm infants at 6 months of corrected age. J Clin Sleep Med. 2023 Dec 1;19(12):2075-2085. doi: 10.5664/jcsm.10760.
PubMed 37559530
Study at a glance
From the registry record, last updated by the sponsor on 6 May 2020. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Influence of Caffeine Therapy in Preterm Infants on Sleep and Neurodevelopmental Outcomes During the First Year of Life: a Single Center Experience
- ClinicalTrials.gov ID
- NCT04376749
- Acronym / sponsor ID
- 09.2019.950
- Conditions
- Caffeine; Sleep Disorder
- Keywords
- caffeine,, sleep wake disorder, preterm, neurodevelopment, actigraphy
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 40 participants (estimated)
- Lead sponsor
- Marmara UniversityUniversity, hospital or other
- Study start
- May 2020 (estimated)
- Primary completion
- May 2021 (estimated)
- Study completion
- May 2021 (estimated)
- First posted
- 6 May 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The development of sleep wake cycles is indicative of child's neurocognitive functions. Caffeine therapy is commonly used in neonatal intensive care units for treatment of apnea of prematurity (AOP), to reduce mechanical ventilation, and improve the success of extubation. In addition, it is suggested to be associated with positive long-term outcomes on pulmonary function and neurodevelopment. However, it is still not clear how caffeine therapy affects the sleep architecture and neurodevelopment of preterm infants. Furthermore, optimal dosing and timing of caffeine therapy is controversial.
We aimed to evaluate the effects of caffeine therapy on sleep architecture and neurodevelopment in preterm infants during the first year of life.
A prospective observational case-control study will be conducted. Forty preterm infants aged between 28 to 34 gestational weeks admitted to the Marmara University Neonatal Intensive Care Unit (NICU) from May 2020 to May 2021 will be included. Infants with neonatal risk factors for poor neurodevelopmental outcomes will be excluded. Duration, timing and cumulative dosage of caffeine therapy will be calculated. Follow up outcome for neurodevelopment and sleep architecture of preterm infants who received caffeine therapy will be compared with those who did not receive caffeine therapy.
Sleep and activity behavior recorded by actigraphy, sleep diary and polysomnography at 6, and 12 months corrected age will be compared to noncaffeine group. Neurodevelopment will be assessed by neurological examination defined by Hammersmith, Ages and Stages Questionnaire (ASQ-2), and Bayley Scales of Infant and Toddler Development.
Detailed description
Methylxanthines have been prescribed in preterm infants to treat and prevent Apnea of Prematurity (AOP), for extubation success, for reduction of incidence of BPD, need for treatment of PDA, retinopathy of prematurity, IVH, and for neuroprotective effects. Caffeine is the most common drug of choice. Despite its frequent use there are no standardized protocols for optimal timing and dosage. It is suggested to have a neuroprotective effect, and associated with reduction of neurological disabilities, cognitive delay. However, there are studies which found no difference in poor neurological outcomes compared to control.
Premature infants have more active sleep compared to term infants, and their sleep patterns mature gradually. Studies about the effects of caffeine therapy on sleep of premature infants are few. It is known that sleep is associated with child's neurodevelopmental outcomes. Identifying the impact of caffeine therapy on sleep will help clinicians to identify and improve neurodevelopmental problems in this vulnerable study population.
The aim of this study is to evaluate the effects of caffeine therapy on sleep, activity patterns and neurodevelopment in preterm infants during the first year of life.
Based on the assumption that each year approximately 20 infants receive neonatal caffeine therapy in the unit, forty preterm infants aged between 28 to 34 gestational weeks admitted to the Marmara University Neonatal Intensive Care Unit (NICU) from May 2020 to May 2021 will be included. Duration, timing and cumulative dosage of caffeine therapy will be calculated. The routine practice of Marmara University NICU protocol is to administer caffeine prophylaxis to infants born at less than 30 weeks of gestational age and/or infants with less than 1250 grams gestational weight. Infants born between 30 to 34 weeks of gestational age who has AOP are treated with caffeine therapy with the commonly prescribed dose of 20 mg/kg loading, and 5-10 mg/kg/day maintenance. Neonatal caffeine therapy continues until the infants are 34 weeks corrected gestational age and free of any apnea episodes for at least 7 days. Infants with neonatal risk factors for poor neurodevelopmental outcomes such as infants with perinatal asphyxia, intraventricular hemorrhage grade 3 or higher, retinopathy of prematurity(ROP) of stage 3 or higher, infants using sedative or anticonvulsant drugs at the time of data collection will be excluded.
Follow up outcome for sleep architecture and neurodevelopment of preterm infants who received caffeine therapy will be compared with those who did not receive caffeine therapy.
Actigraphy Sleep and activity behavior recorded by sleep diary, actigraphy and polysomnography at 6, and 12 months corrected age will be compared to noncaffeine group. Sleep wake patterns will be assessed by Philips Respironics Mini-Mitter Actiwatch-2 for at least 3 days at home environment and sleep diaries within 5-minute intervals will be filled out by parents simultaneously. Actigraphy is a validated wristwatch-like device that distinguishes sleep from wakefulness based on accelerometer measured movement. The actiwatch weighs 16 grams and will be placed on the infant's left ankle. For actigraphy interpretation, if the activity count exceeds a predefined threshold value the epoch is scored as wake state. 10 minutes with no movements on autograph will be determined as sleep phase. High frequency movements with >40 movements in each epoch lasting >10 minutes will be determined as wake state. According to the frequency of infants' movements, a number of sleep-wake variables will be calculated for analyses with Philips Actiware 6.1.8 software. Mean total sleep duration, mean sleep duration during the day, mean sleep duration at night, sleep onset latency (SOL: time taken to fall asleep after reported lights out), wake after sleep onset (WASO: number of minutes recorded as wake between sleep onset and sleep offset), longest consolidated sleep period at night (midnight and 6 am), number of night waking, and sleep efficiency (TST/ time in bed, reported as percent) will be determined.
Polysomnography Infants will undergo 3-4 hours polysomnography (Embla Systems N7000) in the pediatric sleep laboratory. Further validation of the actigraphy will be performed by an epoch-by-epoch comparison of actigraphy and simultaneous polysomnography data. The following variables will be monitored: electroencephalography, electromyography, electrocardiography, heart rate and respiratory rate. Respiration will be monitored with a nasal-cannula- pressure transducer, thoracic and abdominal inductive plethysmography bands and pulse-oximetry. Polysomnography will be recorded with Embla RemLogic software. For polysomnography scoring, recommendations of the American Academy of Sleep Medicine Guidelines-2017 will be followed. The polysomnography data will be analyzed by an expert physician blinded to the actigraphy results or the newborn infant's clinical data, except for gestational age and days of life. Apnea-hypopnea index (AHI) will be determined.
Our secondary objective is to assess neurodevelopment of these infants. Neurodevelopment will be assessed by neurological examination defined by Hammersmith, Ages and Stages Questionnaire (ASQ), and Bayley Scales of Infant and Toddler Development at 6, and 12 months corrected age and will be compared to noncaffeine group.
Neurological examination will be performed with Hammersmith Neurological Examination. Hammersmith Neurological Examination is a quick examination for 3 to 24 months old infants. It consists of 26 items assessing neurological function in 5 groups: cranial nerve function (max 15 points), posture (maximum 18 points), movements (maximum 6 points), tone (maximum 24 points) and reflexes and reactions (maximum 15 points). Each subgroup is scored from 0 to 3 points and all scores are summed at the end of the examination.
Ages and Stages Questionnaire helps to evaluate developmental progress in children between the ages of 1 month and 66 months. Ages and Stages Questionnaire lasts approximately 10-15 minutes and assess the child development in 5 developmental areas: gross motor, fine motor, communication, problem solving and personal- social. Each area consists of 6 questions and the questions are answered in 3 simple responses: yes, sometimes or not yet. The questionnaire is scored with a simple 0, 5- and 10-point scoring system (yes: 10 points, sometimes: 5 points, not yet: 0 points) in 2-3 minutes by parents and the results are interpreted according to standardized cutoffs by professionals. Ages and Stages Questionnaire-2 (ASQ-2) is a parent-friendly developmental scale with 0.86 sensitivity, 0.85 specifity, 0.92 test-retest reliability and 0.93 inter-rater reliability. If the score on any domain is <2SDs below the cut-off point for the Turkish reference group, the child is defined as at risk for neurodevelopmental delay.
The Bayley Scales of Infant and Toddler Development, 3rd Edition produces three composite scores: the Cognitive Scale (range 55-145), the Language scale (range 45-155) which has receptive and expressive communication subtests, and the Motor scale (range 45-155), which consists of Fine Motor, and Gross Motor subtests.
Child's scores will be compared to the standardized age norms.
Study design
- Observational model
- Case-control
- Time perspective
- Prospective
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| preterm infants received caffeine | – | –preterm infants aged between 28 to 34 weeks gestational age who received caffeine therapy either for prophylaxis or treatment |
| preterm infants received no caffeine | – | –preterm infants aged between 28 to 34 weeks gestational age who received no caffeine therapy |
Who may qualify
- Ages
- 28 to 34 weeks
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
- Study population
- Preterm infants born between 28 to 34 gestational weeks admitted to the Marmara University Neonatal Intensive Care Unit (NICU) during one year period
Key inclusion criteria (1 listed)
- Preterm infants born between 28 to 34 gestational weeks admitted to the Marmara University Neonatal Intensive Care Unit (NICU)
Key exclusion criteria (1 listed)
- perinatal asphyxia intraventricular hemorrhage grade 3 or higher retinopathy of prematurity(ROP) of stage 3 or higher major congenital anomalies infants using sedative or anticonvulsant drugs at the time of data collection
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Sleep and activity behavior
Time frame: 6 months corrected age
Sleep and activity behavior recorded by actigraphy
Sleep and activity behavior
Time frame: 12 months corrected age
Sleep and activity behavior recorded by actigraphy
Obstructive Apnea and Hypopnea Index
Time frame: 6 months corrected age
Obstrcutive Apnea and Hypopnea Index recorded by Polysomnography
Obstructive Apnea and Hypopnea Index
Time frame: 12 months corrected age
Obstrcutive Apnea and Hypopnea Index recorded by Polysomnography
3 secondary outcomes
Neurodevelopment
Time frame: 6 and 12 months corrected age
Neurodevelopment
Time frame: 6 and 12 months corrected age
Neurodevelopment
Time frame: 6 and 12 months corrected age
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 6 May 2020.
- Derived from this study: PubMed 37559530Atalah YEY, Baris HE, Akdere SK, Sabanci M, Ozdemir H, Gucuyener K, Eralp EE, Ozek E, Boran P. Effects of caffeine therapy for apnea of prematurity on sleep and neurodevelopment of preterm infants at 6 months of corrected age. J Clin Sleep Med. 2023 Dec 1;19(12):2075-2085. doi: 10.5664/jcsm.10760.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Perran Boran, MD, PhD principal investigator
Marmara University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Caffeine; Sleep Disorder, run by Marmara University at 1 site in Turkey (Türkiye).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 6 May 2020. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Perran Boran, MD, PhD (+905417127756, drperran@yahoo.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Sleep and activity behavior (time frame: 6 months corrected age). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT04376749, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 6 May 2020.