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NCT04952987

Dry Eye Management With 3% Diquafosol Before and After Cataract Surgery

Status unknown Last updated 7 July 2021
What this trial tests

trial testing Diquafosol in Dry Eye in 50 participants. Status unknown.

Timeline
1 January 2021
Primary endpoint
30 December 2021
30 December 2021

Quick facts

Lead sponsorMun Wai Lee
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment50
Start date1 January 2021
Primary completion30 December 2021
Estimated completion30 December 2021
Sites1 location across Malaysia

Drugs / interventions tested

Conditions studied

Sponsor

Mun Wai Lee

Who can join

18 and older, any sex, with Dry Eye. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The objective of this study is to evaluate the efficacy of Diquafosol 3% in the management of dry eyes before and after cataract surgery. Patients with pre-existing dry eyes and planned for cataract surgery will be started on Diquafosol eyedrops prior to surgery and treatment will be continued after cataract surgery. Eligible patients will undergo evaluation of dry eye at baseline and subsequently started on treatment with Diquafosol for the duration of 4 weeks before surgery. Further evaluations will be conducted on the day of surgery and at designated time points during and up to 12 weeks after surgery.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. The developmental journey of therapies targeting purine receptors: from basic science to clinical trials.
    Han S, Suzuki-Kerr H, Vlajkovic SM, Thorne PR. · · 2022 · cited 9× · PMID 36173587 · DOI 10.1007/s11302-022-09896-w

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Other trials of Diquafosol

Trials testing the same drug.

Other recruiting trials for Dry Eye

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04952987.

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