Viewing Study NCT05648058


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Ignite Modification Date: 2025-12-25 @ 10:01 PM
Study NCT ID: NCT05648058
Status: UNKNOWN
Last Update Posted: 2022-12-15
First Post: 2022-12-04
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Role of Nefopam in Rituximab Transfusion Reaction
Sponsor: Ministry Of Health / Nineveh Health Directorate
Organization:

Study Overview

Official Title: Role of Nefopam in Rituximab Transfusion Reaction
Status: UNKNOWN
Status Verified Date: 2022-12
Last Known Status: NOT_YET_RECRUITING
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 patients will be taken nefopam ampule 50 mg before rituximab in the first group while the second group will be taken diphenhydramine ampule 10 mg before rituximab in the second group
Detailed Description: the two groups will be taken standard therapy (hydrocortisone vial 100 mg and acetaminophen 1000 mg) 30 min before rituximab

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
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?: