Viewing Study NCT04629560


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Study NCT ID: NCT04629560
Status: COMPLETED
Last Update Posted: 2020-11-16
First Post: 2020-11-10
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Miracle Fruit Powder for the Treatment of Taste Alterations Secondary to Chemotherapy
Sponsor: Mt. Sinai Medical Center, Miami
Organization:

Study Overview

Official Title: Miracle Fruit Powder for the Treatment of Taste Alterations Secondary to Chemotherapy
Status: COMPLETED
Status Verified Date: 2020-11
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: Purpose and Objective: Compare the incidence of taste alteration in treatment vs. control arms and Compare weight loss in treatment vs. control arms
Detailed Description: After patients is explained all potential risks and study guidelines all patients will be given an ICF to sign if they wish to participate. Once the ICF has been signed by patient approximately between 3-5 days will undergo a screening to determine protocol eligibility. If patients qualifies (eligible) for study patients will be randomly assigned either to the miracle fruit intervention or to supportive measures at first and later participants will cross over to the other intervention

Study Oversight

Has Oversight DMC: False
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?: