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DRKS00013730
Iscrizione alternativa con informazioni locali ulteriori: NCT03083431

Oral Propranolol for prevention of thresholdretinopathy of prematurity

Base di dati: WHO (Importata da 19.12.2024)
Cambiato: 13 dic 2024, 01:01
Categoria di malattie:

Health conditions (Fonte di dati: WHO)


H35.1;Retinopathy of prematurity;H35.1

Interventions (Fonte di dati: WHO)

Group 1: Verum - Oral Propranolol-HCl (1.6 mg/ kg*d) given for 4-10 weeks
Group 2: Placebo - same duration as oral propranolol solution

Inclusion/Exclusion Criteria (Fonte di dati: WHO)

Gender: All
Maximum age: 104 Days
Minimum age: 35 Days
Inclusion criteria: ? Preterm infant born before 28 weeks gestation
? Birth weight below 1250 g
? Alive at 5 weeks of age
? Postmenstrual age 310/7 ? 36 6/7 weeks
? Ophthalmoscopic evidence of incipient ROP (stage 1 or 2, with or without plus disease)
? Written informed consent by parents or legal guardian, including saving and propagation of pseudonymous medical data for study purposes, according to national requirements
Exclusion criteria: ? ROP stage 3 at time of inclusion (endpoint already reached)
? Thyrotoxicosis, arterial hypertension or congenital heart diseases requiring open-label propranolol treatment (such as tetralogy of Fallot, paroxysmal supraventricular tachycardia,
or long QT syndrome)
? Atrio-ventricular block grade 2 or 3 (contraindication for propranolol)
? Sinuatrial block (contraindication for propranolol)
? Uncontrolled heart failure or cardiogenic shock (contraindication for propranolol)
? Acute severe infection (inclusion may be postponed until infection has resolved)
? Bronchial asthma
? Major congenital malformations or known chromosomal anomalies
? Colobomas and other eye malformations
? PHACE syndrome (posterior fossa anomalies, large infantile hemangiomas of the face, neck, and/or scalp, arterial lesions, cardiac abnormalities/coarctation of the aorta, eye anomalies) (risk of cerebrovascular complications)
? Very large hemangioma (risk of hyperkalemia), as judged by the attending physician
? Heart rate consistently (>1 h) < 100/min
? Noninvasive mean arterial pressure consistently (>1 h)
<40 mmHg
? Medication of the infant or the mother if breastfeeding with clonidine, reserpine, angiotensin-converting enzyme inhibitors, angiotensin-receptor antagonists, antiarrhythmic
drugs including amiodarone, propafenone, lidocaine, digoxin/digitoxin, quinidine, verapamil, diltiazem, or bepridil (pharmacodynamic interaction)
? Medication of the infant with rifampicin or phenobarbitone (enhanced metabolic clearance)
? Concurrent treatment with insulin (risk of hypoglycemia)
? Severe liver dysfunction (GPT > 900 U/L)
? Chronic kidney impairment (creatinine > 1.3 mg/dl [100 ?M])
? Persistent hypoglycemia (blood glucose < 36 mg/dl [2.0 mM] in 3 consecutive samples immediately preceding enrollment)
? Persistent hyperkalemia (venous serum potassium > 5.9 mM in 3 consecutive samples immediately preceding enrollment)
? Persistent neutropenia (absolute neutrophil counts <1,000/?L in 3 consecutive samples immediately preceding enrollment)
? Known hypersensitivity to propranolol or any of the excipients
? Prinzmetal?s angina, Raynaud?s phenomenon (severe peripheral arterial circulatory disturbance), or pheochromocytoma (contraindications for propranolol in adults, not occurring in newborn infants)
? Participation in another pharmacological interventional clinical trial
? Any circumstances that make the investigator believe that participation in the study leads to exceptional medical or organizational problems for the patient.

Altri dati sulla sperimentazione nel registro primario dell’OMS

http://drks.de/search/en/trial/DRKS00013730

Altri dati sulla sperimentazione dalla banca dati dell’OMS (ICTRP)

https://trialsearch.who.int/Trial2.aspx?TrialID=DRKS00013730
Altre informazioni sulla sperimentazione

Data di registrazione della sperimentazione

8 gen 2018

Inserimento del primo partecipante

1 giu 2021

Stato di reclutamento

Recruiting withdrawn before recruiting started

Titolo scientifico (Fonte di dati: WHO)

Oral Propranolol for prevention of thresholdretinopathy of prematurity - ROPROP

Tipo di sperimentazione (Fonte di dati: WHO)

interventional

Disegno della sperimentazione (Fonte di dati: WHO)

Allocation: Randomized controlled study; Masking: Blinded (masking used); Control: placebo; Assignment: parallel; Study design purpose: treatment

Fase (Fonte di dati: WHO)

2

Punti finali primari (Fonte di dati: WHO)

Survival without threshold ROP (retinopathy of prematurity) (stage 3 or more)
[time frame: 48 weeks postmenstrual age]
Endpoint: ROP-grade; timepoint: 48 weeks corrected postmenstrual age;
method: ophthalmoscopy

Punti finali secondari (Fonte di dati: WHO)

Survival without ROP treated with ablative laser surgery or intravitreal VEGF antagonists
[time frame: 48 weeks postmenstrual age]

Contatto per informazioni (Fonte di dati: WHO)

BMBF/ DLR Projekttr?ge

Risultati della sperimentazione (Fonte di dati: WHO)

Sintesi dei risultati

ancora nessuna informazione disponibile

Collegamento ai risultati nel registro primario

http://drks.de/search/en/trial/DRKS00013730#studyResults

Informazioni sulla disponibilità dei dati dei singoli partecipanti

No

Siti di esecuzione della sperimentazione

Paesi di esecuzione (Fonte di dati: WHO)

Germany, Israel, Switzerland, Turkey

Contatto per maggiori informazioni sulla sperimentazione

Contatto per informazioni generali (Fonte di dati: WHO)

Charit?platz 1
Charit? - Universit?tsmedizin Berlin, Klinik f?r Neonatologie - CCM
030 450 566 122
rop-rop@charite.de

Contatto per informazioni scientifiche (Fonte di dati: WHO)

Christoph
B?hrer
Augustenburger Platz 1
Charit? - Universit?tsmedizin Berlin, Klinik f?r Neonatologie
030-450 566122
christoph.buehrer@charite.de

Altri numeri di identificazione delle sperimentazioni

Secondary ID (Fonte di dati: WHO)

Iscrizione alternativa con informazioni locali ulteriori: NCT03083431
2017-002124-24
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