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DRKS00013730
Alternative entry with additional local information: NCT03083431

Oral Propranolol for prevention of thresholdretinopathy of prematurity

Data source: WHO (Imported from 19.12.2024)
Changed: Dec 13, 2024, 1:01 AM
Disease category:

Health conditions (Data source: WHO)


H35.1;Retinopathy of prematurity;H35.1

Interventions (Data source: 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 (Data source: 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.

Further information on the trial in WHO primary registry

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

Further information on the trial from WHO database (ICTRP)

https://trialsearch.who.int/Trial2.aspx?TrialID=DRKS00013730
Further information on trial

Date trial registered

Jan 8, 2018

Incorporation of the first participant

Jun 1, 2021

Recruitment status

Recruiting withdrawn before recruiting started

Academic title (Data source: WHO)

Oral Propranolol for prevention of thresholdretinopathy of prematurity - ROPROP

Type of trial (Data source: WHO)

interventional

Design of the trial (Data source: WHO)

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

Phase (Data source: WHO)

2

Primary end point (Data source: 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

Secundary end point (Data source: WHO)

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

Contact information (Data source: WHO)

BMBF/ DLR Projekttr?ge

Trial results (Data source: WHO)

Results summary

no information available yet

Link to the results in the primary register

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

Information on the availability of individual participant data

No

Trial sites

Countries (Data source: WHO)

Germany, Israel, Switzerland, Turkey

Contact for further information on the trial

Contact for general information (Data source: WHO)

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

Contact for scientific information (Data source: WHO)

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

Further trial identification numbers

Secondary ID (Data source: WHO)

Alternative entry with additional local information: NCT03083431
2017-002124-24
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