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Comparison of Compressed Continuous Suture and Conventional Suture in Pterygium Surgery

Comparison of Compression Continuous Suture Versus Conventional Suture for Autologous Conjunctival Implant Fixation in Primary Pterygium Surgery: a Randomized Controlled Trial

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07244276
Enrollment
40
Registered
2025-11-24
Start date
2024-04-02
Completion date
2026-07-02
Last updated
2025-11-24

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

Conditions

Primary Pterygium

Keywords

Primary Pterygium, Compression Continuous Suture, Conventional Suture

Brief summary

To compare the advantages and disadvantages of continuous suture with suture and conventional Suture in primary pterygium surgery for autologous conjunctival graft fixation

Detailed description

Pterygium is an abnormal fibrovascular tissue hyperplasia disease that occurs in the conjunctiva. The pterygium tissue can break through the limbus of the corneosclera and grow into the cornea, causing a foreign body sensation in the eyes, astigmatism, decreased vision, and even restricted eye movement. The purpose of surgical treatment for pterygium is not only to remove the diseased tissue, but more importantly, to reduce the recurrence of pterygium after surgery. Pterygium excision combined with simple autologous conjunctival transplantation is currently the most commonly used method for treating pterygium. The recurrence rate after autologous conjunctival epithelial tissue transplantation can be reduced to 5% to 30%. As heterogenic substances, sutures can irritate the ocular surface, aggravate postoperative inflammatory reactions and conjunctival edema or hemorrhage, delay the repair of corneal wound epithelium, lead to abnormal ocular surface function, intensify postoperative discomfort, and induce hypertrophic granuloma or cysts, etc. Moreover, these adverse reactions can also induce the recurrence of pterygium (0-26%). In addition, the longer the time interval between suture removal, The greater the difficulty of removal, the more likely some of the knots may be completely buried under the conjunctiva. Therefore, in order to alleviate the adverse reactions caused by sutures and further simplify the operation of pterygium excision surgery, many attempts have been made at home and abroad to improve and innovate the method of graft fixation.

Interventions

PROCEDURECompression continuous suture with suture crimping

Pterygium excision combined with autologous conjunctival transplantation was performed, and the continuous suture method with pressure lines was adopted during the operation

PROCEDUREConventional Suture with suture crimping

Pterygium excision combined with autologous conjunctival transplantation was performed, and the traditional suture method was adopted during the operation

Sponsors

Tianjin Eye Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
30 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

1. Diagnosis of primary pterygium according to diagnostic criteria; 2. The pterygium head invades the cornea by 2-5mm; 3. The patient agrees to the surgical treatment and signs the surgical consent form.

Exclusion criteria

1. History of previous eye surgery; 2. Have active ocular inflammatory lesions; 3. recurrent and pseudopterygium; 4. The patient refuses surgery or is unable to have regular follow-ups

Design outcomes

Primary

MeasureTime frameDescription
Duration of surgeryIntraoperativeThe date on which the surgery was performed
Implant stabilityPostoperative follow-up was performed 1 day and 1 week after surgeryWhether the conjunctival graft is loose or detached
Postoperative discomfortPostoperative follow-up was performed 1 day and 1 week after surgeryThe degree of discomfort after surgery was evaluated using the VAS Pain score Scale
Stitch removal timePostoperative follow-up was performed 1 week after surgeryThe date when the stitches were removed

Countries

China

Contacts

Primary ContactYan Wang, director
wangyan7143@vip.sina.com23187165

Outcome results

None listed

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