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The role and comparison of EMLA and 4% tetracaine gel in reducing local anesthetic pain in patients undergoing upper blepharoplasty: A randomized, double-blinded, controlled trial

The role and comparison of EMLA and 4% tetracaine gel in reducing local anesthetic pain in patients undergoing upper blepharoplasty: A randomized, double-blinded, controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300070153
Enrollment
Unknown
Registered
2023-04-03
Start date
2023-04-03
Completion date
Unknown
Last updated
2023-06-26

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

Conditions

local anesthetic injection pain of upper blepharoplasty

Interventions

Blank control group:None
30 Minutes Group(GroupA):Two topical anesthetics were applied to the upper eyelids of both eyes of the subjects in random pairs for 30 minutes
60 Minutes Group(Group B):Two topical anesthetics were applied to the upper eyelids of both eyes of the subjects in random pairs for 60 minutes

Sponsors

The second hospital of Da Lian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients undergoing bilateral upper blepharoplasty.

Exclusion criteria

Exclusion criteria: 1. Age =18 years; 2. Presence of skin wounds in the upper eyelids; 3. History of local anesthetic allergy; 4. Preoperative long-term use of analgetics; 5. History of dermatosis; 6. Pregnant women and lactating women; 7. History of upper eyelid surgery and; 8. Unable to cooperate with the investigation because of understanding problems.

Design outcomes

Primary

MeasureTime frame
local anesthetic injection pain of upper eyelids;

Secondary

MeasureTime frame
local cutaneous reacion;eyelid edema after 24 hours of operation;

Countries

China

Contacts

Public ContactWei Lu

The second hospital of Da Lian Medical University

drluweicn@163.com+86 133 0411 0960

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 6, 2026