Dropless Pars Plana 硝子体切除研究 (DVS)
To demonstrate that intraoperative use of subtenon triamcinolone acetonide at the time of surgery without postoperative eye drops is non-inferior to the regimen of postoperative eye drops following primary pars plana vitrectomy for retinal detachment.
調査の概要
状態
条件
詳細な説明
This is a non-inferiority, single-center, randomized, controlled, open-label clinical trial. Investigators will recruit patients that present to their clinic or emergency department with newly diagnosed mac-on or mac-off rhegmatogenous retinal detachment. Patients will be randomized to one of the following groups:
- Group 1: A total of 84 study subjects (84 eyes) will receive topical antibiotic qid for one week after surgery, topical prednisolone 1% qid tapered by one drop weekly for four weeks (4/3/2/1 taper), and topical atropine 1% daily for one week.
- Group 2: A total of 84 study subjects (84 eyes) will receive sub-tenon injection of triamcinolone acetonide (40 mg/mL) at the time of surgery, with no post-operative eye drops.
Both groups will receive subconjunctival injection of antibiotic (cefazolin 50 mg/0.5 ml, moxifloxacin 0.5 mg/0.1 ml, or vancomycin 1 mg/0.1 ml) and subconjunctival injection of dexamethasone (4 mg/ml) at the time of surgery, as well as atropine 1% and antibiotic-steroid ointment (neomycin-polymyxin B-dexamethasone) at the time of surgery.
研究の種類
入学 (実際)
段階
- フェーズ 4
連絡先と場所
研究場所
-
-
Massachusetts
-
Boston、Massachusetts、アメリカ、02114
- Massachusetts Eye and Ear
-
-
参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
Inclusion Criteria:
- Primary rhegmatogenous retinal detachment (mac-on or mac-off) requiring pars plana vitrectomy (23, 25 and 27-gauge)
Exclusion Criteria:
- Need for concomitant lensectomy or cataract surgery
- Pars plana vitrectomy taking place more than seven days after the initial diagnosis
- History of any prior vitreoretinal surgery (excluding laser surgery) in surgical eye
- History of previous retinal detachment in surgical eye
- History of ocular incisional surgery within six months of surgery (excluding laser surgery) in surgical eye
- History of ocular laser surgery within 1 month in surgical eye
- History of intravitreal injection within 1 month in surgical eye
- Diagnosis of glaucoma or intraocular pressure more than 21 mmHg in either eye
- Active or chronic or recurrent uncontrolled ocular or systemic disease
- Active or history of chronic or recurrent inflammatory eye disease
- Previous history of steroid response
- Current treatment with oral, topical, or intravitreal corticosteroids
- Presence of proliferative vitreoretinopathy at the time of diagnosis
- Presence of giant retinal tear at the time of diagnosis
- Diagnosis of proliferative diabetic retinopathy
- Anterior chamber inflammation on presentation in either eye
- Signs of ocular infection at presentation in either eye
- Acute external ocular infections
- Known or suspected sensitivity or allergy to any of the medications used in the operation or postoperatively
- Inability to use or apply topical eye drops
- Requirement for silicone oil as a tamponade agent
- Individuals with impaired decision-making capacity
- Non-English-speaking subjects
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
アクティブコンパレータ:Group 1
|
Standard of care surgery Antibiotic eye drop 4 times per day for 1 week after surgery
他の名前:
Steroid eye drop 4 times per day tapered by one drop weekly for 4 weeks (4/3/2/1 taper) after surgery
他の名前:
Eye drop daily for 1 week after surgery
他の名前:
|
|
アクティブコンパレータ:Group 2
|
Standard of care surgery Sub-tenon injection of triamcinolone acetonide (40mg/mL) at the time of surgery
他の名前:
|
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Mean anterior chamber cell
時間枠:Day 7 after surgical procedure
|
Mean anterior chamber cell based on SUN (Standardization of Uveitis Nomenclature) criteria as measured by Slit Lamp Biomicroscopy |
Day 7 after surgical procedure
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Mean anterior chamber cell
時間枠:Day 1, 30 and 90 after surgical procedure
|
Mean anterior chamber cell based on Standardization of Uveitis Nomenclature (SUN) criteria as measured by Slit Lamp Biomicroscopy |
Day 1, 30 and 90 after surgical procedure
|
|
Need for rescue medication (corticosteroid)
時間枠:Day 1, 7, 30 and 90 after surgical procedure
|
Need for additional medication (corticosteroid) to control post-operative inflammation |
Day 1, 7, 30 and 90 after surgical procedure
|
|
Intraocular pressure less than 5 or more 30 mmHg
時間枠:Day 1, 7, 30 and 90 after surgical procedure
|
Intraocular pressure measured by applanation tonometer or tono-pen |
Day 1, 7, 30 and 90 after surgical procedure
|
|
Need for medications to reduce intraocular pressure
時間枠:Day 1, 7, 30 and 90 after surgical procedure
|
Need for additional medication to reduce intraocular pressure |
Day 1, 7, 30 and 90 after surgical procedure
|
|
Visual acuity
時間枠:Day 1, 7, 30 and 90 after surgical procedure
|
Best-corrected visual acuity measured using Snellen chart |
Day 1, 7, 30 and 90 after surgical procedure
|
|
Degree of pain
時間枠:Day 1, 7, 30 and 90 after surgical procedure
|
Degree of pain on a pain scale of 1-10 (0: pain free, 10: unspeakable pain) |
Day 1, 7, 30 and 90 after surgical procedure
|
|
Self-reported adherence to positioning
時間枠:Day 1 and 7 after surgical procedure
|
Assessment of self-reported adherence to positioning: "Over the past day or week, what percentage of time or number of hours per day do you think you adhered with the recommended positioning?" |
Day 1 and 7 after surgical procedure
|
|
Self-reported adherence to eye drops
時間枠:Day 1, 7 and 30 after surgical procedure
|
Assessment of self-reported adherence to eye drops in the control group: "Over the past week or month, what percentage of your drops do you think you took correctly?" |
Day 1, 7 and 30 after surgical procedure
|
|
Progression of cataract
時間枠:Day 30 and 90 after surgical procedure
|
Evaluation of progression of cataract by Slit Lamp Biomicroscopy |
Day 30 and 90 after surgical procedure
|
|
Adverse events
時間枠:Day 1, 7, 30 and 90 after surgical procedure
|
Adverse Events including: Endophthalmitis, Re-detachment requiring surgery, Intraocular pressure requiring medication, Need for additional procedures, Any other adverse events |
Day 1, 7, 30 and 90 after surgical procedure
|
協力者と研究者
捜査官
- 主任研究者:Nimesh A. Patel, MD、Massachusetts Eye and Ear
出版物と役立つリンク
一般刊行物
- Paccola L, Jorge R, Barbosa JC, Costa RA, Scott IU. Anti-inflammatory efficacy of a single posterior subtenon injection of triamcinolone acetonide versus prednisolone acetate 1% eyedrops after pars plana vitrectomy. Acta Ophthalmol Scand. 2007 Sep;85(6):603-8. doi: 10.1111/j.1600-0420.2007.00923.x. Epub 2007 Apr 24.
- Brown GT, Karth PA, Hunter AA. Novel Postoperative Dropless Protocol for Micro-Incision Vitrectomy Surgery. Ophthalmic Surg Lasers Imaging Retina. 2021 Nov;52(11):587-591. doi: 10.3928/23258160-20211014-01. Epub 2021 Nov 1.
- Bonfiglio V, Reibaldi M, Macchi I, Fallico M, Pizzo C, Patane C, Russo A, Longo A, Pizzo A, Cillino G, Cillino S, Vadala M, Rinaldi M, Rejdak R, Nowomiejska K, Toro MD, Avitabile T, Ortisi E. Preoperative, Intraoperative and Postoperative Corticosteroid Use as an Adjunctive Treatment for Rhegmatogenous Retinal Detachment. J Clin Med. 2020 May 21;9(5):1556. doi: 10.3390/jcm9051556.
- Assil KK, Greenwood MD, Gibson A, Vantipalli S, Metzinger JL, Goldstein MH. Dropless cataract surgery: modernizing perioperative medical therapy to improve outcomes and patient satisfaction. Curr Opin Ophthalmol. 2021 Jan;32 Suppl 1:S1-S12. doi: 10.1097/ICU.0000000000000708.
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
- 病理学的プロセス
- 病理学的状態、徴候および症状
- 炎症
- ペプチド
- アミノ酸、ペプチド、およびタンパク質
- タンパク質
- 有機化学物質
- 複素環化化合物
- 複素環化化合物、2リング
- 複素環化化合物、融合リング
- 脂質
- アルカロイド
- 多環式化合物
- 妊娠
- 妊娠
- ステロイド
- 融合リング化合物
- ステロイド、フッ素化
- 膜タンパク質
- AZA化合物
- 大環性化合物
- フルオロキノロン
- 4-キノロン
- キノロン
- キノリン
- ペプチド、周期的
- リポペプチド
- 複素環化化合物、ブリッジ型リング
- アトロピン誘導体
- トロパーン
- アザビシクロ化合物
- ベラドンナアルカロイド
- 太陽アルカロイド
- 架橋ビシクロ化合物、複素環
- 抗菌性カチオンペプチド
- 抗菌ペプチド
- 孔形成細胞傷害性タンパク質
- モキシフロキサシン
- アトロピン
- トリアムシノロン
- トリアムシノロンアセトニド
- ポリミキシン
- 酢酸プレドニゾロン
- 1(beta)-D-arabinofuranosylcytosine-5'-diphosphate prednisolone
その他の研究ID番号
- 2022P000046
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
米国で製造され、米国から輸出された製品。
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