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Sponsored by: |
Children's Hospital, San Diego |
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Information provided by: | Children's Hospital, San Diego |
ClinicalTrials.gov Identifier: | NCT00292513 |
Standard suture is superior to both tissue adhesive (2-octyl cyanoacrylate) and absorbable sutures with respect to cosmetic outcome of, complication rate of and parental satisfaction with the closure of low tension facial, neck and shoulder, wounds in children and adolescents
Condition | Intervention |
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Cyst of Face, Neck or Shoulder Pilomatrixoma of Face, Neck or Shoulder |
Device: standard suture (5-0 prolene), topical skin adhesive (dermabond), absorbable suture (5-0 Chromic gut) |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Open Label, Uncontrolled, Parallel Assignment, Efficacy Study |
Official Title: | A Randomized Clinical Trial Comparing Tissue Adhesive (2-Octylcyanoacrylate) Vs. Absorbable Suture Vs. Non-Absorbable Suture for the Closure of Low Tension Facial and Neck Wounds in Children and Adolescents |
Ages Eligible for Study: | up to 18 Years |
Genders Eligible for Study: | Both |
Inclusion Criteria:
Exclusion Criteria:
Contact: Bari B Cunningham, MD | 858-576-1700 ext 4270 | bcunningham@chsd.org |
United States, California | |
Children's Hospital San Diego | Recruiting |
San Diego, California, United States, 92123 | |
Principal Investigator: Bari B Cunningham, MD | |
Sub-Investigator: Sheila F Friedlander, MD | |
Sub-Investigator: Lawrence F Eichenfield, MD | |
Sub-Investigator: Brandie Roberts, MD | |
Sub-Investigator: Magdalene Dohil, MD |
Principal Investigator: | Bari B Cunningham, MD | Children's Hospital, San Diego |
Study ID Numbers: | Dermabond Study |
Study First Received: | February 15, 2006 |
Last Updated: | February 15, 2006 |
ClinicalTrials.gov Identifier: | NCT00292513 |
Health Authority: | United States: Institutional Review Board |
Facies Pilomatrixoma Cysts Neoplasms, Glandular and Epithelial |
Neoplasms Neoplasms by Histologic Type Neoplasms, Basal Cell |