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| ID | Type | Description | Link |
|---|---|---|---|
| 09-N-0193 |
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| Name | Class |
|---|---|
| BCN Peptides | INDUSTRY |
Background:
Objectives:
- To determine if AH-8 can be used as part of a treatment regimen for blepharospasm.
Eligibility:
- Individuals 18 years of age and older who have blepharospasm and have been receiving successful treatment with botulinum toxin injections.
Design:
OBJECTIVE:
To study the efficacy of cutaneous application of Acetyl Hexapeptide-8 (AH8) in the therapy of blepharospasm.
STUDY POPULATION:
22 patients with blepharospasm.
DESIGN:
This will be a double blind, placebo-controlled trial. Patients receiving treatment of blepharospasm with botulinum neurotoxin (BoNT) will be recruited. They will receive either the study substance or a placebo cream containing the emulsion but no active substance, in twice daily applications to the eyelids beginning the day following a BoNT injection treatment. They will continue to apply the cream and we will record the time until their condition worsens back to baseline following benefit from the injections, hypothesizing that the cream application will prolong the time until the need for the next injection by at least 3 months.
OUTCOME MEASURES::
Primary: time until the Jankovic Blepharospasm Rating Scale (JBRS) reverts back to baseline.
Secondary: Change in the JBRS at 6 months; Change in the JBRS at 7 months if not receiving BoNT; Change in the JBRS at 3 months; Change in the Blepharospasm Disability Scale at 6 months
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| active | Experimental | AH-8 containing topical intervention |
|
| placebo | Placebo Comparator | topical intervention WITHOUT AH-8 |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Acetyl-Hexapeptide Topical Treatment | Drug | AH-8 containing topical treatment |
| |
| Measure | Description | Time Frame |
|---|---|---|
| Time Until Jankovic Blepharospasm Rating Scale (JBRS) Reverts Back to Baseline | The JBRS is a severity scale for blepharospasm, ranging from 0 (no symptoms) to 8 (the most severe symptoms, functionally blind). It includes measures of blink frequency and severity of abnormal eye closure. The scale was measured at baseline (before intervention) and followed over time. Return to baseline value represents loss of benefit from BoNT injection. The time to return to baseline JBRS is an indication of added benefit from the topical intervention. | 3-7 months |
| Measure | Description | Time Frame |
|---|---|---|
| Change in the JBRS at 3 Months | The JBRS is a severity scale for blepharospasm, ranging from 0 (no symptoms) to 8 (the most severe symptoms, functionally blind). It includes measures of blink frequency and severity of abnormal eye closure. The scale was measured at baseline (before intervention) and followed over time. | baseline to 3 months |
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INCLUSION CRITERIA:
EXCLUSION CRITERIA:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| National Institutes of Health Clinical Center, 9000 Rockville Pike | Bethesda | Maryland | 20892 | United States |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 15970766 | Background | Ben Simon GJ, McCann JD. Benign essential blepharospasm. Int Ophthalmol Clin. 2005 Summer;45(3):49-75. doi: 10.1097/01.iio.0000167238.26526.a8. No abstract available. | |
| 14871168 | Background | Defazio G, Livrea P. Primary blepharospasm: diagnosis and management. Drugs. 2004;64(3):237-44. doi: 10.2165/00003495-200464030-00002. |
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| ID | Title | Description |
|---|---|---|
| FG000 | Active | Topical intervention agent containing AH8 0.005% Twice daily application to the eyelids in standardized fashion. |
| FG001 | Placebo | Topical intervention agent WITHOUT AH-8. Identically appearing cream without the active ingredient. Twice daily application to the eyelids in standardized fashion. |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
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| ID | Title | Description |
|---|---|---|
| BG000 | Active | AH-8 containing topical intervention |
| BG001 | Placebo | topical intervention WITHOUT AH-8 |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Categorical | Count of Participants |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Time Until Jankovic Blepharospasm Rating Scale (JBRS) Reverts Back to Baseline | The JBRS is a severity scale for blepharospasm, ranging from 0 (no symptoms) to 8 (the most severe symptoms, functionally blind). It includes measures of blink frequency and severity of abnormal eye closure. The scale was measured at baseline (before intervention) and followed over time. Return to baseline value represents loss of benefit from BoNT injection. The time to return to baseline JBRS is an indication of added benefit from the topical intervention. | Posted | Mean | Standard Deviation | month | 3-7 months |
|
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Active | AH-8 containing topical intervention |
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| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| eyelid irritation | Skin and subcutaneous tissue disorders | Systematic Assessment | 4 subjects (2 active arm and 2 placebo arm) experience minor self-limited eyelid irritation. Ophthalmology consultation was obtained in all cases. No change in the study procedure was needed. |
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| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Codrin Lungu, MD | Office of the Clinical Director, NINDS, NIH | 301-496-5295 | lunguci@ninds.nih.gov |
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| ID | Term |
|---|---|
| D020821 | Dystonic Disorders |
| D004421 | Dystonia |
| D001764 | Blepharospasm |
| ID | Term |
|---|---|
| D009069 | Movement Disorders |
| D002493 | Central Nervous System Diseases |
| D009422 | Nervous System Diseases |
| D020820 | Dyskinesias |
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| placebo |
| Drug |
topical treatment NOT containing AH-8 |
|
| % Blepharospasm Disability Scale (BDS) Change at 3 Months |
% BDS change at 3 months. The BDS is a quality of life scale ranging from 0 (no symptoms) to 26 (maximum impact of symptoms on quality of life). The questions are specific for impairment related to blepharospasm. We compared the percentage change over three months in the active and placebo arms. |
| baseline to 3 months |
| 11835433 | Background | Defazio G, Livrea P. Epidemiology of primary blepharospasm. Mov Disord. 2002 Jan;17(1):7-12. doi: 10.1002/mds.1275. |
| BG002 |
| Total |
Total of all reporting groups |
| Participants |
|
| Age Continuous | Mean | Standard Deviation | years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
subjects receiving placebo intervention, ie identically-appearing topical cream without AH-8 content
|
|
| Secondary | Change in the JBRS at 3 Months | The JBRS is a severity scale for blepharospasm, ranging from 0 (no symptoms) to 8 (the most severe symptoms, functionally blind). It includes measures of blink frequency and severity of abnormal eye closure. The scale was measured at baseline (before intervention) and followed over time. | One placebo arm participant dropped out due to unrelated personal problems | Posted | Mean | Standard Deviation | points | baseline to 3 months |
|
|
|
| Secondary | % Blepharospasm Disability Scale (BDS) Change at 3 Months | % BDS change at 3 months. The BDS is a quality of life scale ranging from 0 (no symptoms) to 26 (maximum impact of symptoms on quality of life). The questions are specific for impairment related to blepharospasm. We compared the percentage change over three months in the active and placebo arms. | One placebo arm participant discontinued study due to unrelated personal problems | Posted | Mean | Standard Deviation | percentage change | baseline to 3 months |
|
|
|
| 0 |
| 12 |
| 2 |
| 12 |
| EG001 | Placebo | topical intervention WITHOUT AH-8 | 0 | 12 | 2 | 12 |
|
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| D009461 |
| Neurologic Manifestations |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D005141 | Eyelid Diseases |
| D005128 | Eye Diseases |