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A Prospective Double-blind Interventional Study of Tissue Reaction to Polyglycolic Acid Sutures in Human Skin

A Prospective Double-blind Interventional Study of Tissue Reaction to Polyglycolic Acid Sutures in Human Skin

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01598376
Enrollment
42
Registered
2012-05-15
Start date
2010-06-30
Completion date
2011-03-31
Last updated
2012-05-15

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

Conditions

Lower Eyelid Entropion

Keywords

entropion, suture, granuloma, tissue reaction

Brief summary

Objective To investigate the tissue reaction produced by implanted polyglactin suture material in normal human skin and to determine the effect of suture gauge on this response. Design A prospective, double blind, randomized clinical trial using a novel ethical study design. Both the patient and clinician analyzing the histology were blinded to the suture gauge used. Participants A total of 42 consecutive patients presenting to an oculoplastic clinic with involutional entropion and horizontal eyelid laxity, who provided written consent to participate, were enrolled in the study. Intervention Patients were randomly allocated to 5/0 or 7/0 Vicryl™ test suture groups. Patient symptoms were alleviated during the wait for definitive surgery by the placement of temporary eyelid everting sutures including a test suture. After 28 days, entropion correction was achieved by a Quickert procedure which includes excision of an eyelid wedge. Histological analysis was carried out, blind to the suture gauge used, on the excised eyelid containing the test suture. Main outcome measure Defined histological parameters of suture-related granulomas were measured at multiple levels. Data included granuloma outer diameter, central cellular diameter, giant cell number and area of fibrous coat (calculated from the coat diameter and thickness at multiple levels) and a statistical comparison made between the 5/0 and 7/0 suture gauge groups.

Interventions

PROCEDURE7/0 vicryl suture

7/0 vicryl test suture placed as one of 3 everting sutures

PROCEDURE5/0 vicryl test suture

5/0 vicryl test suture placed as one of 3 everting sutures

Sponsors

The Royal Bournemouth Hospital
Lead SponsorOTHER

Study design

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

Eligibility

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

Inclusion criteria

* Consecutive patients * Involutional lower eyelid entropion * Horizontal eyelid laxity associated * Informed consent

Exclusion criteria

* Inability to provide informed consent * Previous eyelid surgery * Poorly controlled diabetes * Oral steroid use * Addisons disease

Design outcomes

Primary

MeasureTime frameDescription
Suture associated granuloma outer diameter28 daysHistological measurement of suture associated granuloma outer diameter on excised eyelid specimens, average of 6 sections examined
Suture associated granuloma central cellular element diameter28 daysHistological measurement of suture associated granuloma central cellular element diameter on excised eyelid specimens, average of 6 sections examined
Suture associated granuloma fibrous coat area28 daysHistological measurement of suture associated granuloma fibrous coat area on excised eyelid specimens, average of 6 sections examined
Suture associated granuloma giant cell number28 daysCount of giant cells on average of 6 histological sections from excised eyelid specimens

Countries

United Kingdom

Outcome results

None listed

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