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NCT00882232 · ClinicalTrials.gov registry record · Phase 1

Cross-linked Hyaluronan Gel Reduces Rectal Toxicity Due to Radiation Therapy for Prostate Cancer

A Phase 1 study, sponsored by Cancer Center of Irvine.

Completed
Registry status
Phase 1
Development phase
10
Enrollment target

NCT00882232: Completed Phase 1 study, sponsored by Cancer Center of Irvine.

NCT00882232 is a Phase 1 study that has completed, run by Cancer Center of Irvine. The registered enrollment target is 10 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (83% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT00882232, a Phase 1 study, has completed, sponsored by Cancer Center of Irvine.

COMPLETED
Registry status
Phase 1
Development phase
10 participants
Enrollment target

Study Summary

The primary purpose of this study is to determine if cross-linked hyaluronan gel reduces the dose of radiation delivered to the rectum and the rectal toxicity of radiotherapy for localized prostate cancer.

Interventions

  • DEVICE Cross-linked hyaluronan gel

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2008-09
Est. Completion 2009-09
Phase Phase 1
Cancer Center of Irvine

3 total trials

What the finished NCT00882232 record still lists

NCT00882232 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (83% lower).

The record links to 0 conditions, and to 1 intervention - of which Cross-linked hyaluronan gel is the first listed.

NCT00882232 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00882232 about?

NCT00882232 is a clinical study titled "Cross-linked Hyaluronan Gel Reduces Rectal Toxicity Due to Radiation Therapy for Prostate Cancer". The primary purpose of this study is to determine if cross-linked hyaluronan gel reduces the dose of radiation delivered to the rectum and the rectal toxicity of radiotherapy for localized prostate cancer.

What is the current status of trial NCT00882232?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 10 participants. The study started on 2008-09. Estimated completion is 2009-09.

What interventions are being tested in trial NCT00882232?

The interventions under investigation include: Cross-linked hyaluronan gel (DEVICE).

Who is sponsoring clinical trial NCT00882232?

This trial is sponsored by Cancer Center of Irvine, which has 3 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00882232's enrollment target sits among peer trials

10 1913th of 2000 higher than 46 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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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Source: ClinicalTrials.gov NCT00882232, the US trial registry maintained by the National Library of Medicine. NCT00882232 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.