Intravitreal Ranibizumab in Recurrent ROP

Sponsor
Ameera Gamal Abdelhameed (Other)
Overall Status
Completed
CT.gov ID
NCT04539106
Collaborator
(none)
115
1
8
14.3

Study Details

Study Description

Brief Summary

A retrospective study included reviewing of medical records of preterm babies who were admitted in neonatal intensive care unit (NICU) of Mansoura University children hospital (MUCH) or referred from nearby hospitals for ROP screening during the period from March 2013 to February 2020.

Condition or Disease Intervention/Treatment Phase
  • Drug: intravitreal injection of Ranibizumab

Detailed Description

Retinopathy of prematurity was diagnosed and classified according to the International Classification of ROP. Data of the patients who received IVR for type 1 ROP or aggressive posterior ROP (AP-ROP) according to early treatment ROP study (ETROP) were collected. Intravitreal ranibizumab injection was performed as follows; topical anesthetic drop was applied, standard aseptic eye preparation with 5% betadine was performed, a lid speculum was inserted and intravitreal injection of 0.25 mg/0.025 ml ranibizumab with a 30-gauge needle 1.5mm from limbus was given. In case of bilateral ROP, both eyes are injected in the same session. Infants were examined a day after the procedure and weekly thereafter until full vascularization of the retina was observed.

ROP reactivation was defined as any of the following: recurrent plus disease, recurrent neovascularization, or reformation of ridge despite treatment . Once recurrence was determined, second injection of IVR (0.25mg/0.025mL) was given to patients or surgery was performed if progressed to stage 4 or 5. All treated infants were examined until complete regression of ROP and full retinal vascularization.

Study Design

Study Type:
Observational
Actual Enrollment :
115 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Clinical Outcome Following Reinjection of Ranibizumab in Recurrent Cases With Retinopathy of Prematurity
Actual Study Start Date :
Jun 1, 2019
Actual Primary Completion Date :
Feb 1, 2020
Actual Study Completion Date :
Feb 1, 2020

Outcome Measures

Primary Outcome Measures

  1. full vascularization of the retina [6 months]

    Infants were examined a day after the procedure and weekly thereafter until full vascularization of the retina was observed.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • patients received IVR for type 1 ROP or aggressive posterior ROP (AP-ROP) according to early treatment ROP study (ETROP) and developed recurrence of ROP
Exclusion Criteria:

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mansoura University Mansoura Dakahlia Egypt

Sponsors and Collaborators

  • Ameera Gamal Abdelhameed

Investigators

  • Principal Investigator: Rania MR Bassiouny, MD, Mansoura University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Ameera Gamal Abdelhameed, Lecturer of Ophthalmology, Mansoura University
ClinicalTrials.gov Identifier:
NCT04539106
Other Study ID Numbers:
  • intravitreal Ranibizumab reinj
First Posted:
Sep 4, 2020
Last Update Posted:
Sep 4, 2020
Last Verified:
Aug 1, 2020
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 4, 2020