Adjunctive Local Application of Lidocaine During Scleral Buckling Under General Anesthesia

Status

UNKNOWN

Phases

Phase 4

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT01417572

Enrollment

Registered

2011-08-16

Start date

2010-01-31

Completion date

2011-09-30

Last updated

2011-08-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Retinal Detachment

Brief summary

The purpose of this study is to evaluate the effect of topical lidocaine in scleral buckling surgery.

Interventions

DRUGlidocaine

to evaluate the effect of lidocaine on oculocardiac reflex during the surgery

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender

ALL

Age

20 Years to 60 Years

Healthy volunteers

Yes

Inclusion criteria

* Retinal detachment * Retinal tear less than 3 hour clock

Exclusion criteria

* Vitreous hemorrhage * Proliferative vitreoretinopathy

Design outcomes

Primary

Measure	Time frame
decrease in pain and nausea,vomiting after surgery	6 month
decrease in ocr after application of topical lidocaine	6 month
postoperative nausea and vommitting	6 month
postoperative pain	6 month
intraoperative heart rate measurement	6 month

Countries

Iran

Contacts

Primary ContactAmin Masjedi, MD

Masjedi1827@gmail.com+983112211915

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026