Intravitreal injections are used more and more frequently in ophthalmology. This trend is mostly caused by the arrival of anti-VEGF agents used for age-related macular degeneration, diabetic macular edema and macular edema secondary to retinal vein…
ID
Bron
Aandoening
intravitreal, intraocular, injection, pain, crossover.
intravitreaal, intraoculair, injectie, pijn.
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
Pain score on 100mm numeric rating scale.
Achtergrond van het onderzoek
Rationale:
Pain and discomfort at the injection site are common side effects of intravitreal injections with bevacizumab. In current practice 30 gauge needles are regularly used for these intravitreal injections and they have been shown to cause less pain than thicker needles.
Objective:
The main objective of this study is to evaluate whether pain caused by intravitreal bevacizumab injections with the regular 30 gauge needle can be reduced by using a 33 gauge needle.
Study design:
Double-blind, randomized, cross-over trial.
Study population:
Patients eligible for treatment with two consecutive injections with intravitreal bevacizumab.
Intervention:
All patients receive two consecutive intravitreal injections with bevacizumab 1.25 mg in 0.05 ml as decided by their treating physician. Patients are randomized to receive the first intravitreal injection either with the regular 30 gauge or the 33 gauge needle. The interval for the second injection will be 2-6 weeks and will be performed using the alternate injection needle.
Study endpoints:
The primary outcome is the degree of pain during the intravitreal injection, as measured on a 100 mm numeric rating scale (NRS) of pain intensity. The secondary endpoint is anxiety experienced during the injection procedure determined using the hospital anxiety depression scale (HADS) and the state-trait anxiety inventory (STA-I).
Burden and risks associated with participation:
Patients are asked to fill in a HADS and STA-I questionnaire prior to the two consecutive injections and to score the degree of pain experienced during the intravitreal injections on a 100 mm NRS immediately after the procedure. There are no known risks associated with a higher needle gauge. Patients will be informed of the risks related to the injection procedure itself, namely endophthalmitis, retinal detachment and increased risk of cataract, which are the same as in normal clinical practice and are unlikely to be associated with needle gauge.
Doel van het onderzoek
Intravitreal injections are used more and more frequently in ophthalmology. This trend is mostly caused by the arrival of anti-VEGF agents used for age-related macular degeneration, diabetic macular edema and macular edema secondary to retinal vein occlusion. It is known from clinical practice that discomfort and pain at the injection site are common side effects from intravitreal injections. In current practice 30 gauge needles are often used for intravitreal injections with bevacizumab and they have been shown to cause less pain and vitreal reflux than thicker needles. We expect pain level can be lowered even further by reducing needle width to 33 gauge.
Onderzoeksopzet
Injection nr 1 at timepoint 0 and injection nr 2 after 1 month.
Onderzoeksproduct en/of interventie
Two consecutive intraocular bevacizumab injections with a 33G and 30G needle.
Publiek
F. Asten, van
Nijmegen 6525 EX
The Netherlands
+31 (0)24 3610241
F.vanAsten@ohk.umcn.nl
Wetenschappelijk
F. Asten, van
Nijmegen 6525 EX
The Netherlands
+31 (0)24 3610241
F.vanAsten@ohk.umcn.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
Patients with an indication for at least two consecutive monthly intravitreal injections with bevacizumab.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
Patients unable to state pain levels or give written informed consent.
Opzet
Deelname
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In overige registers
Register | ID |
---|---|
NTR-new | NL3611 |
NTR-old | NTR3770 |
Ander register | METC : 2012/259 |
ISRCTN | ISRCTN wordt niet meer aangevraagd. |