Anecortave Acetate Injection to Treat Steroid-responsive Intraocular Pressure Increase in Cornea Transplant Patients
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| ClinicalTrials.gov Identifier: NCT00884039 |
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Recruitment Status :
Terminated
(Preliminary data analysis showed insufficient efficacy to justify continuation.)
First Posted : April 20, 2009
Results First Posted : November 17, 2010
Last Update Posted : August 14, 2018
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Transplant Intraocular Pressure | Drug: anecortave acetate Drug: 30 mg anecortave acetate | Not Applicable |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 7 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Double (Participant, Outcomes Assessor) |
| Primary Purpose: | Treatment |
| Official Title: | Compassionate Use of Anecortave Acetate: Clinical Protocol for the Treatment of Corticosteroid-induced Intraocular Pressure (IOP) Increases After Corneal Transplantation |
| Study Start Date : | May 2009 |
| Actual Primary Completion Date : | August 2010 |
| Actual Study Completion Date : | September 2010 |
| Arm | Intervention/treatment |
|---|---|
| Active Comparator: 30 mg anecortave acetate |
Drug: 30 mg anecortave acetate
anterior juxtascleral depot of 30mg anecortave acetate |
| Active Comparator: 15 mg anecortave acetate |
Drug: anecortave acetate
anterior juxtascleral depot of 15 mg anecortave acetate |
- Intraocular Pressure Within Normal Limits (<24 mm Hg) [ Time Frame: 1 month ]Intraocular pressure was measured by Goldmann applanation tonometry.
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| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- at least 18 years of age
- corneal transplant recipient with intraocular pressure (IOP) greater than 24 mmHg and with relative increase in IOP of at least 10 mmHg over the pre-graft baseline
Exclusion Criteria:
- not pregnant or lactating
- intraocular surgery in the study eye within 30 days before enrolling in the study
- use of any investigational drug or treatment within 30 days before receipt of study medication
- clinical evidence of scleral thinning
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00884039
| United States, Indiana | |
| Price Vision Group | |
| Indianapolis, Indiana, United States, 46260 | |
| Principal Investigator: | Francis W. Price, Jr., MD | Cornea Research Foundation of America |
| Responsible Party: | Cornea Research Foundation of America |
| ClinicalTrials.gov Identifier: | NCT00884039 |
| Other Study ID Numbers: |
2007-12 |
| First Posted: | April 20, 2009 Key Record Dates |
| Results First Posted: | November 17, 2010 |
| Last Update Posted: | August 14, 2018 |
| Last Verified: | July 2018 |
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