Use of an Oxidized Regenerated Cellulose After Thyroid Surgery: A Prospective, Randomized Study

The purpose of this study is to evaluate the effects and safety of oxidized, regenerated cellulose as an absorbable adhesion barrier after thyroidectomy.

Completed

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Key information

Conditions

Thyroidectomy

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Seoul National University College of Medicine

Seoul, 110-744, South Korea

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

operable thyroid neoplasm

Exclusion criteria

a history of previous neck surgeries or uncontrolled medical diseases such as hyperthyroidism, diabetes, and hypertension
administration of non-steroidal anti-inflammatory drugs (NSAIDs) or anti-platelet agents within 1 week before surgery

Treatment and study plan

application of oxidized regenerated cellulose

Device

Sponsors and collaborators

Lead sponsor

Seoul National University Hospital

Other

Registry information

Acronym: ORC

Important dates

First posted: Jul 28, 2010
Registry last updated: Jul 28, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed