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Self-adherent Wrap Techniques for Orbital Surgery

Folded and Classic Techniques of Self-adherent Wrap for Eyes After Orbital Tumour Extirpation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03415490
Enrollment
128
Registered
2018-01-30
Start date
2018-01-19
Completion date
2018-04-21
Last updated
2018-05-02

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

Conditions

Eye Diseases, Surgery

Keywords

general anesthesia, self-adherent wrap, pressure

Brief summary

The purpose of this study is to evaluate the interface pressure measurements of applying self-adherent wraps on eyes after orbital tumour extirpation.

Detailed description

The purpose of this study is to evaluate the interface pressure measurements of the folded and classic techniques of applying self-adherent wraps on eyes after orbital tumour extirpation.

Interventions

OTHERFolded technique of self-adherent wrap

Wrapping a piece of self-adherent wrap around the patient's head starting with the opened end on the forehead above the affected eye.The bandage is then firmly but not tightly wrapped around the head twice. Then, after the second circuit, the bandage is brought on the cheek and up over the eye to the forehead, where it was passed between the eyebrows but not wrapped around the head. Instead, the bandage is folded and then first passed back on the cheek of the affected side then back to the forehead a total of four times. Finally, the bandage is wrapped completely around the head once

OTHERClassic technique of self-adherent wrap

Wrapping a piece of self-adherent wrap around the patient's head starting with the opened end on the forehead above the affected eye.The bandage is then firmly but not tightly wrapped around the head twice. After the second circuit, the bandage was brought below the ear, up over the eye and around the head of the non-affected side and then wrapped around the head in the same manner four times. The bandage is then brought around the head once.

Sponsors

Sun Yat-sen University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
16 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* over 16 years old * diagnosed as orbital disease or ocular tumor * surgery under general anesthesia

Exclusion criteria

* any uncontrolled clinical problems

Design outcomes

Primary

MeasureTime frameDescription
the pressure on the affected eye10 minutes after bandage application in awake individualsthe pressure on the affected eye using the two methods

Secondary

MeasureTime frameDescription
the pressure outside the affected eye10 minutes after bandage application in awake individualsthe pressure outside the affected eye using the two methods
discomfort scores1 minute after recording the pressuresDiscomfort levels were measured using Numerical Rating Scale (NRS) ranging from 0 to 10, where 0 represents no discomfort and 10 represents the worst discomfort; this scale has been confirmed to be sensitive and reliable. Discomfort was defined as sensation other than pain and included nausea, vomiting, headache, and dizziness. Clinically significant postoperative discomfort was considered serious discomfort (NRS score ≥5) any time postoperatively.

Countries

China

Outcome results

None listed

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