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OpenTrials
Completed

NCT Number: NCT06111170

Effect of Compression Dressing After Upper Eyelid Blepharoplasty on Edema, Ecchymosis, Pain and Ocular Surface Irritation

Study to analyze whether there is a difference in postoperative outcome regarding edema, ecchymosis, pain, OSI and discomfort of the patients after blepharoplasty if a compression dressing is used or not.

Completed

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Key information

Conditions

Dermatochalasis of Eyelid

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Augenklink LMU

München, Germany

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with upper eyelid dermatochalasis who were scheduled for upper eyelid blepharoplasty

Exclusion criteria

  • previous surgery on the upper eyelid, previous eye lid trauma, congenital lid changes, blepharochalasis syndrome, coagulation disorders or indication for combined ptosis and blepharoplasty surgery

Treatment and study plan

Compression dressing

Device

Application of dressing

Primary outcomes

  1. Edema

    Time frame: Measures are taken the first day after surgery (D1), one week after surgery (D7) and eight weeks after surgery (D56)

    Degree of edema postoperatively, rated on a four point rating scale: 0 = no, 1 = minimal, 2 = moderate, 3 = severe

Sponsors and collaborators

Lead sponsor

Augenklinik LMU

Other

Registry information

Important dates

Study start
2020
Primary completion
2023
Study completion
2023
First posted
Nov 1, 2023
Registry last updated
Nov 1, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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