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DRKS00013730
Alternativer Eintrag mit zusätzlichen lokalen Informationen: NCT03083431

Oral Propranolol for prevention of thresholdretinopathy of prematurity

Datenbasis: WHO (Import vom 19.12.2024)
Geändert: 13.12.2024, 01:01
Krankheitskategorie:

Health conditions (Datenquelle: WHO)


H35.1;Retinopathy of prematurity;H35.1

Interventions (Datenquelle: 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 (Datenquelle: 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.

Weitere Angaben zur Studie im WHO-Primärregister

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

Weitere Angaben zur Studie aus der Datenbank der WHO (ICTRP)

https://trialsearch.who.int/Trial2.aspx?TrialID=DRKS00013730
Weitere Informationen zur Studie

Datum der Studienregistrierung

08.01.2018

Einschluss der ersten teilnehmenden Person

01.06.2021

Rekrutierungsstatus

Recruiting withdrawn before recruiting started

Wissenschaftlicher Titel (Datenquelle: WHO)

Oral Propranolol for prevention of thresholdretinopathy of prematurity - ROPROP

Studientyp (Datenquelle: WHO)

interventional

Design der Studie (Datenquelle: WHO)

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

Phase (Datenquelle: WHO)

2

Primäre Endpunkte (Datenquelle: 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

Sekundäre Endpunkte (Datenquelle: WHO)

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

Kontakt für Auskünfte (Datenquelle: WHO)

BMBF/ DLR Projekttr?ge

Ergebnisse der Studie (Datenquelle: WHO)

Zusammenfassung der Ergebnisse

noch keine Angaben verfügbar

Link zu den Ergebnissen im Primärregister

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

Angaben zur Verfügbarkeit von individuellen Teilnehmerdaten

No

Studiendurchführungsorte

Durchführungsländer (Datenquelle: WHO)

Germany, Israel, Switzerland, Turkey

Kontakt für weitere Auskünfte zur Studie

Kontakt für allgemeine Auskünfte (Datenquelle: WHO)

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

Kontakt für wissenschaftliche Auskünfte (Datenquelle: WHO)

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

Weitere Studienidentifikationsnummern

Secondary ID (Datenquelle: WHO)

Alternativer Eintrag mit zusätzlichen lokalen Informationen: NCT03083431
2017-002124-24
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