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Clinical observation of three types of surgical treatments for primary pterygium

Clinical observation of three types of surgical treatments for primary pterygium

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800016416
Enrollment
Unknown
Registered
2018-06-01
Start date
2018-12-31
Completion date
Unknown
Last updated
2018-06-05

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

Conditions

Primary pterygium

Interventions

group 1:Pterygium excision combined with amniotic membrane transplantation
group 2:Excision of pterygium combined with conjunctival autograft with limbal stem cells
group 3:Pterygium excision combined with amniotic membrane transplantation and limbal stem cell transplantation

Sponsors

Beijing Tongren Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) aged 18-70 years men and women; (2) patients with pterygium surgery meet the following criteria: primary pterygium; The head of pterygium to the length of cornea < 4mm; (3) the laboratory results were in the following range: the upper limit of the normal value of aspartate aminotransferase (AST) below 1.5 times (ULN), the upper limit of the normal value of alanine aminotransferase (ALT) less than 1.5 times (ULN), and the upper limit of normal value of serum creatinine (Cr) less than 1 times (ULN); (4) voluntary signing of the letter of informed consent.

Exclusion criteria

Exclusion criteria: (1) lactating or pregnant women, or planned pregnancies; (2) other drugs that may affect the corneal epithelial growth and metabolism during the first 4 weeks of screening (such as befushu, gaintshu, Deproteinised Calf Serum Eye Gel, etc.); (3) patients with serious systemic organic diseases; (4) abnormal eye diseases such as eyelid, tear, conjunctiva and corneal stem cells, such as severe eyelid insufficiency, dry eye disease, and angular conjunctival chemical injury stem cell dysfunction are greater than those of 1/2 quadrant; (5) screening in the first 3 months to participate in or are participating in other clinical trials; (6) people with mental illness; (7) poor compliance; (8) the researchers believe that there are any patients who are not suitable for inclusion.

Design outcomes

Primary

MeasureTime frame
BUT;shirmmer test 1;Corneal epithelium healing;Recurrence of pterygium;Amniotic membrane dissolving;

Secondary

MeasureTime frame
vision;

Countries

China

Contacts

Public ContactYing Jie

Eye department of Beijing Tongren Hospital, Capital Medical University

jie_yingcn@aliyun.com+86 13693572296

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026