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
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Chemotherapeutic agent A(Docetaxel),B(Cisplatin) or C(Docetaxel) plus Dietary Supplement (RaproCell) | Chemotherapeutic side effect elimination without adversely effecting the Chemotherapeutic agent drug. |
| DRUG | Chemotherapeutic agent A(Docetaxel),B(Cisplatin) or C(Docetaxel) plus placebo | Placebo |
| DRUG | Chemotherapeutic 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
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT05137067. Inclusion in this directory is not an endorsement.