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NCT01771991 · ClinicalTrials.gov registry record · NA
Study of Topical Superoxide Dismutase to Treat Radiation Induced Fibrosis
A NA study, sponsored by Sanford Health.
- Completed
- Registry status
- NA
- Development phase
- 74
- Enrollment target
NCT01771991: Completed NA study, sponsored by Sanford Health.
NCT01771991 is a NA study that has completed, run by Sanford Health. The registered enrollment target is 74 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01771991, a NA study, has completed, sponsored by Sanford Health.
- COMPLETED
- Registry status
- NA
- Development phase
- 74 participants
- Enrollment target
Study Summary
The purpose of this study is to determine if topical superoxide dismutase is an effective treatment of radiation related neck fibrosis, and to determine the quality of life impact from radiation related fibrosis in the head and neck cancer patients at Sanford Health.
Primary Outcome
Number of participants with improvement in fibrosis as defined as a one point improvement on the fibrosis scale using the grading scale outlined in CTCAE 4.03, page 46.
Interventions
- DRUG Placebo
- DRUG Topical Sodermix Dismutase in the form of Sodermix (SOD)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 74 participants |
| Start Date | 2012-08 |
| Est. Completion | 2013-06 |
| Phase | NA |
What the finished NCT01771991 record still lists
NCT01771991 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 74 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower).
The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.
NCT01771991 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01771991 about?
NCT01771991 is a clinical study titled "Study of Topical Superoxide Dismutase to Treat Radiation Induced Fibrosis". The purpose of this study is to determine if topical superoxide dismutase is an effective treatment of radiation related neck fibrosis, and to determine the quality of life impact from radiation related fibrosis in the head and neck cancer patients at Sanford Health.
What is the current status of trial NCT01771991?
This trial is currently completed. It is a NA study. The enrollment target is 74 participants. The study started on 2012-08. Estimated completion is 2013-06.
What interventions are being tested in trial NCT01771991?
The interventions under investigation include: Placebo (DRUG), Topical Sodermix Dismutase in the form of Sodermix (SOD) (DRUG).
Who is sponsoring clinical trial NCT01771991?
This trial is sponsored by Sanford Health, which has 34 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01771991's enrollment target sits among peer trials
74 1082nd of 2000 higher than 912 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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