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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01350024
Enrollment
34
Registered
2011-05-09
Start date
2011-05-01
Completion date
2016-07-30
Last updated
2017-05-30

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

Conditions

Blepharoptosis

Keywords

Conjunctival Mullerectomy, Blepharoptosis, Ptosis surgery, Pain Control

Brief 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.

Interventions

PROCEDUREFrontal nerve block with 2% lidocaine with 1:100,000 dilution of epinephrine

Frontal Nerve Block 5 cc will be administered preoperatively once.

PROCEDURESubconjunctival injection of 2% lidocaine with 1:100,000 dilution with epinephrine

Patients will receive a 1.5 cc dose of subconjunctival lidocaine as above

Sponsors

University of Miami
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
Yes

Inclusion criteria

* 18 years of age and older * Patient with ptosis that requires correction * Patient is able to consent for themselves

Exclusion criteria

* Patient unable to complete survey * Patient had prior lid surgery * Patient taking chronic pain medication

Design outcomes

Primary

MeasureTime frameDescription
Pain control24 hour after surgeryPatients will be asked to complete a survey regardning pain assessment twenty-four hours after completion of surgery.

Secondary

MeasureTime frameDescription
Efficacy of ptosis surgery2 monthsStandard measures include marginal reflex distanced, palpebral fissure and levator fucntion will be used to assess the efficacy of the ptosis surgery and compared to the type of anesthesia the patient was given.
Pain Control1 hour after surgerycompletion of survey to assess pain after surgery has been completed.

Countries

United States

Outcome results

None listed

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