CClinicalTrials.gg
Status unknownNCT00443105Updated Mar 5, 2007

Topical Tacrolimus 0.03% Ointment for Intractable Allergic Conjunctivitis: An Open Label Pilot Study

A Phase 2 interventional study of Tacrolimus 0.03% ointment (Protopic) in Allergic Conjunctivitis, sponsored by Assaf-Harofeh Medical Center. Status unknown at 1 site in Israel. Open to participants aged 5 Years and older. Per ClinicalTrials.gov, last updated 2007-03-05.

Sponsored by Assaf-Harofeh Medical Center · Phase 2, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Dec 2006), so the status shown — last known as Active, not recruiting — may be out of date.
Phase
Phase 2
Study type
Interventional
Allocation
Non-randomized
Ages
5 Years and older
Sex
All
01

Study summary

The purpose of this study is to determine the efficacy, tolerance and safety of tacrolimus 0.03% ointment in the treatment of intractable allergic conjunctivitis.

02

Conditions studied

  • Allergic Conjunctivitis
03

In context

Conjunctivitis

361 studies on the registry are indexed under Conjunctivitis; 17 are open to participants now.

Browse Conjunctivitis studies →

Lead sponsor

Assaf-Harofeh Medical Center is the lead sponsor of 258 studies on the registry; 40 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
5 Years and older
Sexes eligible
All

Inclusion criteria

  • Subjects included if they were > 5 years old and suffered from intractable allergic conjunctivitis

Exclusion criteria

Exclusion Criteria:

  • pregnancy or breastfeeding,history of herpetic eye disease,transplant patients concomitant administration of drugs inhibiting cytochrome CYP3A4, hypersensitivity to macrolides
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Single group
Masking
None (open label)

Interventions

  • DrugTacrolimus 0.03% ointment (Protopic)
06

Study locations

1 site
  • Assaf Harofeh Medical Center, Department of Ophthalmology
    Zerifin, 70300, Israel
07

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 5, 2007, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
08

Registry details

Key details

Study ID
NCT00443105
Lead sponsor
Assaf-Harofeh Medical Center
First posted
Mar 5, 2007
Last update
Mar 5, 2007

Study contacts

David Zadok, MD
principal investigator · Assaf Harofeh Medical Center, Tel Aviv University

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Dec 2006. You cannot join it, but the record below documents what was studied.

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