Ignite Creation Date:
2024-05-05 @ 7:33 PM
Last Modification Date:
2024-10-26 @ 9:50 AM
Study NCT ID:
NCT00693654
Status:
COMPLETED
Last Update Posted:
2018-09-10
First Post:
2008-06-05
Brief Title:
Comparative Study of the Efficacy of SARNA Sensitive Lotion for Treatment of Uremic Itch in Adult Hemodialysis Patients
Sponsor:
Wake Forest University
Organization:
Wake Forest University Health Sciences
Study Overview
Official Title:
A Controlled Comparative Study of the Efficacy of SARNA Sensitive Lotion for Treatment of Uremic Pruritus in Adult Hemodialysis Patients
Status:
COMPLETED
Status Verified Date:
2018-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The purpose of this research study is to evaluate the efficacy of SARNA Sensitive Lotion in the treatment of uremic pruritus in adult hemodialysis patients in a double-blind Controlled comparative trial
Detailed Description:
This was a 4-week randomized double-blind controlled study Fourteen subjects received treatment lotion 1 pramoxine HCl and the remaining 14 received a bland emollient Cetaphil lotion A target lesion limited to one anatomic site excluding face and genitals was selected at baseline Each subject was instructed to apply lotion twice daily to all affected areas of pruritus for four weeks The use of any other topical or systemic medication to treat uremic pruritus was not permitted while participating in the study Subjects were clinically evaluated for erythema xerosis lichenification and overall severity at baseline week 1 and week 4 end of study
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
True
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| 31648 | OTHER | WakeForest | None |