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Polyglactin Sutures Versus Nylon Sutures for Suturing of Conjunctival Autograft in Pterygium Surgery: a Randomised Controlled Trial
This study has been completed.
First Received: October 23, 2006   Last Updated: December 15, 2008   History of Changes
Sponsored by: Hospital Authority, Hong Kong
Information provided by: Hospital Authority, Hong Kong
ClinicalTrials.gov Identifier: NCT00391573
  Purpose

To compare the use of polyglactin sutures versus nylon sutures for conjunctival autograft suturing in pterygium surgery.


Condition Intervention
Pterygium
Procedure: Polyglactin sutures for suturing of conjunctival autograft in pterygium surgery
Procedure: Nylon sutures for suturing of conjunctival autograft in pterygium surgery

MedlinePlus related topics: Surgery
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Single Blind, Active Control, Single Group Assignment, Efficacy Study
Official Title: Polyglactin Sutures Versus Nylon Sutures for Suturing of Conjunctival Autograft in Pterygium Surgery: a Randomised Controlled Trial

Further study details as provided by Hospital Authority, Hong Kong:

Primary Outcome Measures:
  • The difference in VAS score between the two groups

Secondary Outcome Measures:
  • Graft hyperemia, oedema and tarsal conjunctival papillary hypertrophy
  • Surgical complications
  • Pterygium recurrence

Estimated Enrollment: 32
Study Start Date: March 2005
Estimated Study Completion Date: June 2005
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Inclusion criteria included patients with primary nasal pterygium, aged 18 years or older, and able to cooperate surgery under local anaesthesia.

Exclusion Criteria:

  • Patients with recurrent pterygium, scarred superior conjunctiva, previous surgery involving the superior bulbar conjunctiva, history of glaucoma, and cicatricial ocular surface disease were excluded
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00391573

Locations
China
Hong Kong Eye Hospital
Hong Kong, China
Sponsors and Collaborators
Hospital Authority, Hong Kong
Investigators
Principal Investigator: Victoria Wong, Dr Hong Kong Eye Hospital
  More Information

Additional Information:
No publications provided

Study ID Numbers: KC/KE-05-0008, HARECCTR0500063
Study First Received: October 23, 2006
Last Updated: December 15, 2008
ClinicalTrials.gov Identifier: NCT00391573     History of Changes
Health Authority: Hong Kong: Ethics Committee

Study placed in the following topic categories:
Eye Diseases
Pterygium of the Conjunctiva
Pterygium
Conjunctival Diseases

Additional relevant MeSH terms:
Eye Diseases
Pterygium
Conjunctival Diseases

ClinicalTrials.gov processed this record on May 07, 2009