Botulinum Toxin for Treatment of Seborrhic Dermatitis in Parkinsonian Patients
NCT00767546 · Status: UNKNOWN · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 40
Last updated 2008-10-07
Summary
There's high incidence of seborrhic dermatitis among patients suffering from Parkinson's disease. Seborrhic dermatitis is caused by increased exertion of sebaceous glands. Previous studies have shown an increase of sebum excretion rate in parkinsonian pateints. Other studies demonstrated improvement in seborrhic dermatitis after anticholinergic treatment. From these studies we concluded that there might be hyperactivity of the parasympathetic system among PD patients, that cause increased exertion of sebum, therefore local injection of botulinium toxin, which inhibitis acetyl choline realese, might improve the rash of seborrhic dermatitis.
40 patients suffering from Parkinson disease or other parkinsonian disorders will participate in this study.
Before treating the patients with botulinium toxin, we will measure the sebum exertion with the sebumeter device and make clinical evaluation of the rash. We will also take a picture of the rash.
Then Botulinium toxin (60- 100 units) will be locally injected to the rash area.
Two weeks after the injection the patients will be called and evaluated clinicly and by the sebumeter. Then they will be checked again after 3 weeks, after a month and after two, three and four month's.
Conditions
- Parkinson Disease
- Parkinsonism
- Seborrheic Dermatitis
Interventions
- DRUG
-
Botulinum toxin
60- 100 units Local injection to the rash area
Sponsors & Collaborators
-
Rabin Medical Center
lead OTHER
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2009-05-31
- Primary Completion
- 2010-08-31
- Completion
- 2010-08-31
More Related Trials
-
Tocotrienols in Parkinson's Disease (PD)
NCT04491383 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE2
-
A Placebo- and Active Controlled Study of Preladenant in Subjects With Moderate to Severe Parkinson's Disease (P04938)
NCT01155466 ·Status: COMPLETED ·Phase: PHASE3
-
ACP-103 to Treat Parkinson's Disease
NCT00086294 ·Status: COMPLETED ·Phase: PHASE2
-
Rotigotine Patch in Subjects With Advanced Stage, Idiopathic Parkinson's Disease Who Are Not Well Controlled on Levodopa
NCT00244387 ·Status: COMPLETED ·Phase: PHASE3
-
Multicenter Study of Rasagiline in Parkinson's Disease Patients Using Levodopa and Experiencing Motor Fluctuations
NCT00203034 ·Status: COMPLETED ·Phase: PHASE3
-
A Safety, Tolerability, and Plasma Concentration Study of Levodopa/Carbidopa Subcutaneous Solution (ND0612) in Parkinson's Disease (PD) Patients
NCT01725802 ·Status: COMPLETED ·Phase: PHASE1
-
Safety, Tolerability and Effects of Mannitol in Parkinson's Disease
NCT03823638 ·Status: UNKNOWN ·Phase: PHASE2
-
SLV308 for Treatment of Patients With Early Parkinson's Disease
NCT00269516 ·Status: COMPLETED ·Phase: PHASE3
-
Repurposing Lithium for Parkinson's Disease: a RCT
NCT06339034 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE1/PHASE2
-
ADX48621 for the Treatment of Levodopa Induced Dyskinesia in Patients With Parkinson's Disease
NCT01336088 ·Status: COMPLETED ·Phase: PHASE2
-
Rasagiline as Add on to Dopamine Agonists in the Treatment of Parkinson's Disease
NCT01049984 ·Status: COMPLETED ·Phase: PHASE4
-
A Study of LY3154207 in Healthy Participants and Participants With Parkinson's Disease
NCT02562768 ·Status: COMPLETED ·Phase: PHASE1
-
Rasagiline for Gait Treatment
NCT01098396 ·Status: UNKNOWN
-
Study to Assess the Safety of MRx0029 or MRx0005 Compared to Placebo, in People With Parkinson's
NCT05832775 ·Status: WITHDRAWN ·Phase: PHASE1
-
A Fourteen-Week Placebo-Controlled Dose-Response Efficacy and Safety Study of NS 2330 in Early Parkinson's Disease Patients (Study for Proof of Concept in Early Parkinson's Disease of a Triple Reuptake Inhibitor, NS 2330 / SCEPTRE)
NCT00148486 ·Status: COMPLETED ·Phase: PHASE2
-
Sarizotan in Parkinson Patients With L-dopa-induced Dyskinesia
NCT00314288 ·Status: COMPLETED ·Phase: PHASE2
-
A Phase 3 Study of TVP-1012 (1 mg) in Early Parkinson's Disease Patients
NCT02337725 ·Status: COMPLETED ·Phase: PHASE3
-
Nilotinib in Parkinson's Disease
NCT03205488 ·Status: COMPLETED ·Phase: PHASE2
-
An Active-Controlled Extension Study to NCT01155466 [P04938] and NCT01227265 [P07037] (P06153)
NCT01215227 ·Status: TERMINATED ·Phase: PHASE3
-
Repurposing Lithium for Parkinson's Disease
NCT06099886 ·Status: COMPLETED ·Phase: PHASE1
-
Treatment of Parkinson's Disease With Eliprodil
NCT00001929 ·Status: COMPLETED ·Phase: PHASE2
-
Nilotinib in Cognitively Impaired Parkinson Disease Patients 001
NCT02281474 ·Status: COMPLETED ·Phase: PHASE1
-
Preliminary Study of Piclozotan in Patients With Motor Complications Associated With Parkinson's Disease
NCT00623363 ·Status: COMPLETED ·Phase: PHASE2
-
NBI-98854 Dose Titration Study for the Treatment of Tardive Dyskinesia
NCT01733121 ·Status: COMPLETED ·Phase: PHASE2
-
Continuously Infused Intracerebral (IC) Recombinant-Methionyl Human Glial Cell Line-Derived Neurotrophic Factor (r-metHuGDNF) for the Treatment of Idiopathic Parkinson's Disease
NCT00006488 ·Status: COMPLETED ·Phase: PHASE1