NCT01706848View on ClinicalTrials.gov

Celotres for Improvement in Wound Healing and Resulting Scar Consequences Following Suturing of a Wound

NACompletedINTERVENTIONAL
Enrollment

60

Participants

Timeline

Start Date

September 30, 2012

Primary Completion Date

May 31, 2014

Study Completion Date

May 31, 2014

Conditions
Scar
Interventions
OTHER

Celotres

Surgical procedure will be performed as per the standard of care. Scar halves randomized to treatment with device (Celotres), opposite side treated per standard of care.

OTHER

Surgical Closure by Standard of Care

Surgical procedure will be performed as per the standard of care. Scar halves randomized to treatment with device (Celotres), opposite side treated per standard of care.

Trial Locations (9)

Unknown

Angelius Szpital Proviat, Katowice

Oddzial Leczenia Oparzen Chirugil Plastysznej, Krakow

Wojskowy Oddzial Kliniczny ChirurgiiPlastycznej, Warsaw

B15 3SJ

The Westbourne Center, Birmingham

CM15 8EH

Brentwood Hospital, Brentwood

W1G9LG

Plastic Surgery W1 Ltd, Suite 1, London

NE1 4LP

Royal Victoria Infirmary, Newcastle upon Tyne

NR4 7UY

Norfolk and Norwich University Hospital, Norwich

SA6 6NL

Morriston Hospital, Swansea

All Listed Sponsors
lead

Halscion, Inc.

INDUSTRY

NCT01706848 - Celotres for Improvement in Wound Healing and Resulting Scar Consequences Following Suturing of a Wound | Biotech Hunter | Biotech Hunter