ACTRN12620001207909Completed未知
A single blinded, prospective randomised controlled trial of evaluation of wound healing and pain at post-operative dressing change between skin closure with synthetic polybutester sutures and octyl cyanoacrylate tissue adhesive in patients who have elective open forefoot surgery
St Vincent's Hospital Sydney0 sites84 target enrollmentStarted: November 13, 2020Last updated:
Conditions
Trial Snapshot
- Phase
- 未知
- Status
- Completed
- Sponsor
- Enrollment
- 84
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
- Allocation
- Randomised controlled trial
- Primary Purpose
- Treatment
- Masking
- Blinded (masking used)
Eligibility Criteria
- Ages
- 18 Years to o limit (—)
- Sex
- All
Inclusion Criteria
- •The inclusion criteria for this study were:
- •- Age greater than 18 years
- •- Undergoing elective open forefoot surgery; either Scarf ± Akin osteotomy for hallux valgus or first metatarsophalangeal joint arthrodesis)
- •- Informed consent for participation in the RCT
Exclusion Criteria
- •The exclusion criteria for this study were:
- •- Revision forefoot surgery
- •- Percutaneous forefoot surgery
- •- Patients undergoing surgery not involving the first ray
- •- Cognitive impairment preventing patient from adhering to post operative instructions or completing patient reported outcome scores
Investigators
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