Clinical Trials Directory

Trials / Completed

CompletedNCT05137067

A Novel Approach for Alleviating the Side Effects of Chemotherapeutic Agents.

Effectiveness of RaproCell in Alleviating the Side Effects of Chemotherapeutic Agents, Without Adversely Impacting the Overall Success of the Agents on Cancer Cells.

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
90 (actual)
Sponsor
Optimal Health Research · Academic / Other
Sex
All
Age
25 Years – 75 Years
Healthy volunteers
Not accepted

Summary

This study will assess the effectiveness of a natural nutraceutical in treating the known side effects of chemotherapeutic agents in cancer patients.

Detailed description

This study will assess the effectiveness of a natural nutraceutical in treating the known side effects of chemotherapeutic agents in cancer patients. The study will be observing the standard treatment protocol for any degradation or enhancement due to the nutraceutical.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTChemotherapeutic agent A(Docetaxel),B(Cisplatin) or C(Docetaxel) plus Dietary Supplement (RaproCell)Chemotherapeutic side effect elimination without adversely effecting the Chemotherapeutic agent drug.
DRUGChemotherapeutic agent A(Docetaxel),B(Cisplatin) or C(Docetaxel) plus placeboPlacebo
DRUGChemotherapeutic agent A(Docetaxel),B(Cisplatin) or C(Docetaxel).Chemotherapeutic agent A(Docetaxel),B(Cisplatin) or C(Docetaxel).

Timeline

Start date
2021-01-20
Primary completion
2022-10-18
Completion
2023-05-25
First posted
2021-11-30
Last updated
2025-03-21

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT05137067. Inclusion in this directory is not an endorsement.