Clinical Trials Directory

Trials / Unknown

UnknownNCT05616507

Oligo-Fucoidan Decrease Lung Radiation Damage

A Phase II Trial of Oligo-Fucoidan in Radiation Induced Ling Injury

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Taipei Medical University WanFang Hospital · Academic / Other
Sex
All
Age
20 Years – 90 Years
Healthy volunteers
Not accepted

Summary

Fucoidan is FDA approved and in common use for treatment of angina. These studies will advance that work to human use. Successful mitigation of lung radiation damage and heart toxicity will improve the quality of life in veterans and non-veterans who are treated for lung cancer by radiation, and may also improve cure rates of radiation therapy for lung cancer.

Detailed description

This project will test the effect of Fucoidan to mitigate the lung damage that can occur as a side effect of radiation therapy for lung cancer. Thousands of veterans develop lung cancer every year, and are treated by radiation therapy. Studies of lung radiation injury in laboratory animals show that with Fucoidan, investigators can significantly reduce the severity of lung fibrosis and heart toxicity.1,2 Fucoidan is FDA approved and in common use for treatment of angina. These studies will advance that work to human use. Successful mitigation of lung radiation damage and heart toxicity will improve the quality of life in veterans and non-veterans who are treated for lung cancer by radiation, and may also improve cure rates of radiation therapy for lung cancer.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTfucoidanIt is recommended to consume on an empty stomach, 2 servings per day, a total of 8 tablets, which can be eaten at one time or in divided doses. If it is difficult to swallow, the powder in the capsule can also be taken out and mixed with food or liquid food.

Timeline

Start date
2022-03-30
Primary completion
2024-12-30
Completion
2025-12-30
First posted
2022-11-15
Last updated
2022-11-15

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT05616507. Inclusion in this directory is not an endorsement.