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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01171079
Other study ID # ORC-100
Secondary ID
Status Completed
Phase N/A
First received July 26, 2010
Last updated July 27, 2010

Study information

Verified date July 2010
Source Seoul National University Hospital
Contact n/a
Is FDA regulated No
Health authority Korea: Institutional Review Board
Study type Interventional

Clinical Trial Summary

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


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender Both
Age group 18 Years to 70 Years
Eligibility 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

Study Design

N/A


Related Conditions & MeSH terms


Intervention

Device:
application of oxidized regenerated cellulose


Locations

Country Name City State
Korea, Republic of Seoul National University College of Medicine Seoul

Sponsors (1)

Lead Sponsor Collaborator
Seoul National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

References & Publications (2)

Yigit O, Uslu Coskun B, Coskun H, Yilmaz B, Alkan S, Cinar U, Dadas B. Efficacy of anti-adhesive barriers in secondary thyroidectomy: an experimental study. Laryngoscope. 2004 Sep;114(9):1668-73. — View Citation

Yilmaz O, Genc A, Taneli F, Demireli P, Deliaga H, Taneli C. Assessment of the efficacy of absorbable adhesion barriers on dissection in esophagus operations. Int J Pediatr Otorhinolaryngol. 2007 Mar;71(3):409-14. Epub 2006 Dec 11. — View Citation

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