This study is being conducted to assess the utility of hyperbaric oxygen as an adjunctive treatment to reduce postoperative complications. It is hypothesized that HBO2 given in the immediate postoperative period will reduce postoperative complications in patients undergoing below-the-knee amputations. The objective of this study will be to compare treatment and standard care groups, randomly created of eligible patients, to compare their postoperative complications and to assess their postoperative hospital length of stay, 90-day mortality, failure to heal at 4 and 8 week follow-up visits and ability to ambulate with a prosthesis at 6 months post amputation.
This is a clinical study to test the hypothesis that Hyperbaric Oxygen (HBO2) given in the immediate postoperative period for a total of 10 treatments after Below-the-Knee Amputation (BKA) for vascular disease will reduce postoperative complications. Patients scheduled for BKA at Duke University Medical Center will be reviewed for contraindications to HBO2. Patients for whom HBO2 is not contraindicated may choose to be enrolled in the study. Patients enrolled will be randomly assigned to receive treatment or standard postoperative care. Each patient receiving treatment will receive twice daily HBO2 for 2 hours at breathing 100% oxygen at 2 atmospheres absolute (ATA). Patients receiving HBO2 will breathe 100% oxygen via head tent while inside a hyperbaric chamber at Duke University Hospital. The statistical plan for this study will test non-directional hypotheses (two-sided tests). Bonferroni correction will be used to adjust for multiple tests. The main analysis of the primary efficacy hypotheses will include data from all randomized patients in the group to which random assignment is made. Hence, the analysis will be intention to treat. This study will primarily aim to assess whether patients receiving treatment suffer fewer complications, as defined by the Vascular Quality Initiative, vs. patients who receive standard care. The Vascular Quality Initiative (VQI) is a multicenter voluntary reporting system for outcomes related to vascular surgery. The primary outcome of this study, postoperative complications, will be those outcomes meeting the definition set out in the VQI data dictionary, the set of definitions for inclusion in the VQI database. This allows for a standard definition of complications recognized by a majority of US academic medical centers. Secondary outcomes include hospital length of stay, 90-day mortality, failure to heal at 4 and 8 week follow-up visits and ability to ambulate with a prosthesis at 6 months post amputation.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
4
Hyperbaric oxygen (HBO2) 1-2 times daily for up to 10 times after amputation
Duke University Medical Center
Durham, North Carolina, United States
Number of Participants With Mortality During the Inpatient Period
Time frame: During inpatient stay immediately after amputation, up to 13 days
Number of Participants With Re-operation
Unplanned return to the OR (operating room) for a surgical procedure
Time frame: Up to 90 days after amputation
Number of Participants With Wound Infection
Any wound site infection that was culture positive or required antibiotic treatment
Time frame: Up to 90 days after amputation
Hospital Length of Stay
Hospital length of stay immediately after amputation
Time frame: up to approximately 30 days
Number of Participants With 90-day Mortality
Death within 90 days after amputation
Time frame: Up to 90 days after amputation
Number of Participants With Complete Healing of Amputation Wound Healing at 4 Weeks Following Surgery
Complete wound healing at 4 weeks after amputation
Time frame: 4 weeks after amputation
Number of Participants With Complete Healing of Amputation Wound Healing at 8 Weeks Following Surgery
Complete wound healing at 8 weeks after amputation
Time frame: 8 weeks after amputation
Number of Participants Able to Ambulate With Prosthesis
Ability to ambulate with a prosthesis at 6 months post amputation
Time frame: 6 months after amputation
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