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NCT01350024 · ClinicalTrials.gov registry record · NA

Comparison of Postoperative Pain With Two Different Types of Local Anesthesia in Surgery for a Drooping Eyelid

A NA study, sponsored by University of Miami.

Completed
Registry status
NA
Development phase
34
Enrollment target

NCT01350024: Completed NA study, sponsored by University of Miami.

NCT01350024 is a NA study that has completed, run by University of Miami. The registered enrollment target is 34 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01350024, a NA study, has completed, sponsored by University of Miami.

COMPLETED
Registry status
NA
Development phase
34 participants
Enrollment target

Study Summary

Conjunctival Mullerectomy is a well known procedure used to correct upper lid ptosis via a posterior approach. Patients who undergo this procedure are often given local anesthesia to alleviate intraoperative and postoperative pain. Local anesthesia can be given via frontal nerve block or subconjunctival injection combined with sedation in most cases. Both techniques are currently acceptable options for local anesthesia, however postoperative pain has not been systematically evaluated between these two techniques. The investigators aim to compare intra-operative and postoperative pain with these two techniques in patients undergoing conjunctival Mullerectomy for ptosis repair. Patients will be randomized to receive local anesthesia via frontal nerve block or via subconjunctival injection. In addition, the investigators will measure the surgical outcomes of the ptosis surgery with standard measures.

Primary Outcome

Patients will be asked to complete a survey regardning pain assessment twenty-four hours after completion of surgery.

Interventions

  • PROCEDURE Frontal nerve block with 2% lidocaine with 1:100,000 dilution of epinephrine
  • PROCEDURE Subconjunctival injection of 2% lidocaine with 1:100,000 dilution with epinephrine

Trial Details

FieldValue
Enrollment Target 34 participants
Start Date 2011-05-01
Est. Completion 2016-07-30
Phase NA
University of Miami

721 total trials

What the finished NCT01350024 record still lists

NCT01350024 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 34 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 2 interventions - of which Frontal nerve block with 2% lidocaine with 1:100,000 dilution of epinephrine is the first listed.

NCT01350024 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01350024 about?

NCT01350024 is a clinical study titled "Comparison of Postoperative Pain With Two Different Types of Local Anesthesia in Surgery for a Drooping Eyelid". Conjunctival Mullerectomy is a well known procedure used to correct upper lid ptosis via a posterior approach. Patients who undergo this procedure are often given local anesthesia to alleviate intraoperative and postoperative pain. Local anesthesia can be given via frontal nerve block or subconjunct...

What is the current status of trial NCT01350024?

This trial is currently completed. It is a NA study. The enrollment target is 34 participants. The study started on 2011-05-01. Estimated completion is 2016-07-30.

What interventions are being tested in trial NCT01350024?

The interventions under investigation include: Frontal nerve block with 2% lidocaine with 1:100,000 dilution of epinephrine (PROCEDURE), Subconjunctival injection of 2% lidocaine with 1:100,000 dilution with epinephrine (PROCEDURE).

Who is sponsoring clinical trial NCT01350024?

This trial is sponsored by University of Miami, which has 721 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01350024's enrollment target sits among peer trials

34 1570th of 2000 higher than 427 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01350024, the US trial registry maintained by the National Library of Medicine. NCT01350024 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.