Nylon Versus Chromic Gut Sutures for Minor Hand Surgery

Randomized Controlled Trial Comparing Nylon and Chromic Gut Sutures After Minor Hand Surgery

This study aims to assess the relationship between overall satisfaction with treatment in a group of randomized patients undergoing elective hand surgery using either absorbable (4-0 Chromic) or non-absorbable (5-0 Nylon) sutures. The investigators will also assess factors associated with wound concerns, pain intensity, magnitude of limitations, and physical function within one month of surgery.

Inclusion Criteria:

• All patients undergoing common day-case elective hand surgery under local anesthesia, one of the following (initial) procedures:

  • Carpal tunnel release
  • Trigger finger release
  • Ganglion excision
  • Excisional biopsy
  • De Quervain release
  • Dupuytren fasciectomy
  • Any other minor hand surgery

• Patients aged 18-89

• Able to provide informed consent

• Able to understand English or Spanish to complete questionnaires

• Patients who have an email-address or phone number (needed for follow-up)

• UT Health Austin Musculoskeletal Institute, Austin Regional Clinic, Orthopaedic Specialists of Austin.

• Available for follow-up contact after 4 weeks

Exclusion Criteria:

• Patients not able to give informed consent
• Patients using corticosteroids
• Patients with one of the following comorbidities: bleeding disorder, immunodeficiency, collagen vascular disease.
• Patients known to be allergic to suture materials
• Revision procedures