Status unknownNCT01417572Updated Aug 16, 2011

Adjunctive Local Application of Lidocaine During Scleral Buckling Under General Anesthesia

A Phase 4 interventional study of lidocaine in Retinal Detachment, sponsored by Isfahan University of Medical Sciences. Status unknown at 1 site in Iran, Islamic Republic of. Open to participants aged 20 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2011-08-16.

Sponsored by Isfahan University of Medical Sciences · Phase 4, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Jan 2010), so the status shown — last known as Recruiting — may be out of date.

Phase: Phase 4
Study type: Interventional
Enrollment: 30
Allocation: Randomized
Ages: 20 Years to 60 Years
Sex: All

Study summary

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

Conditions studied

Retinal Detachment

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Retinal Detachment 207

In context

Retinal Detachment

207 studies on the registry are indexed under Retinal Detachment; 27 are open to participants now.

This study's planned enrollment of 30 is below the median of 50 across 136 interventional studies indexed under Retinal Detachment.

Browse Retinal Detachment studies →

Lead sponsor

Isfahan University of Medical Sciences is the lead sponsor of 145 studies on the registry; 8 are open to participants now.

Counted across the registry records on this site, refreshed daily.

Who can participate

Ages eligible: 20 Years to 60 Years
Sexes eligible: All
Accepts healthy volunteers: Yes

Inclusion criteria

Retinal detachment
Retinal tear less than 3 hour clock

Exclusion criteria

Exclusion Criteria:

Vitreous hemorrhage
Proliferative vitreoretinopathy

Study design

Phase: Phase 4
Primary purpose: Treatment
Allocation: Randomized
Intervention model: Parallel assignment
Masking: Triple (Participant, Care provider, Investigator)
Enrollment: 30 participants (estimated)

Study arms

Experimental
lidocaine
Drug: lidocaine

Interventions

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

What researchers measure

Primary outcomes

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

Study locations

1 of 1 sites recruiting

Isfahan University of Medical Sciences
Isfahan, 7864329800, Iran, Islamic Republic of
- amin masjedi, MD · Contact · Masjedi1827@gmail.com · +983112211915
- Amin Masjedi, MD · Principal investigator
Recruiting

Updates

Tracking since Sep 25, 2026

No changes since tracking began. The registry record was last updated on Aug 16, 2011, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗

Registry details

Key details

Study ID: NCT01417572
Lead sponsor: Isfahan University of Medical Sciences
First posted: Aug 16, 2011
Start date: Jan 2010
Primary completion: Aug 2010
Completion: Sep 2011 (estimated)
Last update: Aug 16, 2011

Study contacts

Amin Masjedi, MD

Contact

Masjedi1827@gmail.com

+983112211915

View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Jan 2010. You cannot join it, but the record below documents what was studied.

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