Skip to content

Oral Zinc Therapy for the Prevention of Mucositis

A Ramdomized Double Blined Placebo Controlled Oral Zinc Therapy for the Prevention of Mucositis in Patients Undergoing High Dose Chemotherapy With Stem Cell Support

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00449592
Enrollment
40
Registered
2007-03-20
Start date
2007-04-30
Completion date
2008-09-30
Last updated
2008-10-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mucositis

Keywords

Stem cell transplantation, Mucositis, Zinc

Brief summary

Zinc is an intracellular mineral with important enzymatic cofactor activities for cell membrane stability, DNA and RNA structure. Zinc deficiency is associated with delayed wound healing and immune dysfunction. In patietns with hematological malignancies an inverse correlation was found between disease stage and zinc level. Patients undergoing high dose chemotherapy for hematologic malignancies are predisposed to develop oral and gastrointestinal complications, in particular oral mucositis. These patients may have relative zinc deficiency, therefore oral zinc therapy may be benefical in the prevention of these complications.

Detailed description

Patients candidate for High dose chemotherapy with stem cell support for the diagnosis of relapsed/resistant Hodgkins or NHL or MM will be screened for enrollment in the study. Patients will be randomized in a 1:1 ratio to therapy with either zincol 1 Tab TID or placebo 1 Tab TID. Therapy will start on the morning before commencing chemotherapy and will continue untill the first of either discharge day or day 21. Response assesment will include: 1. Mucositis assesment using NCI-CTC and OMAS scores- to be done eod from baseline and untill day 21/discharge day if before day 21 2. Evaluation of zinc levels in the serum, PBMC and saliva- to be done at baseline, day 6/7 and day 21/discharge day if before day 21. 3. Collection of clinical outcome data regarding infectious complications including- presence and length of febrile neutropenia,use of antibacterial and antifungal medications,

Interventions

DRUGZinc

Oral Zincol 1 Tab TID from day -6/-7 until discharge

DRUGPlacebo

Oral placebo 1 Tab TID from day -6/-7 until discharge

Sponsors

Sheba Medical Center
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Patients undergoing high dose chemotherapy with stem cell support for relapsed or resistant Hodgkins or NHL (treated with BEAM protocol) or MM (treated with high dose melphalan). * ECOG performance less than or equal to 2 * Adequate renal and hepatic function

Exclusion criteria

* Presence of any other active malignancy other than BCC of the skin

Design outcomes

Primary

MeasureTime frame
Maximal Mucositis gradeday -7 to day +21 or discharge day

Secondary

MeasureTime frame
Duration of maximal mucositis gradeday -7 to day +21 or discharge day
Overall duration of mucositisday -7 to day +21 or discharge day
Duration of severe neutropeniaday -7 to day +21 or discharge day
Duration of febrile neutropeniaday -7 to day +21 or discharge day

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026