Randomized Clinical Study for Core and Topical Warming of the Open Wound Cavity With Warmed Humidified CO2 Versus Control in Colon Surgery
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 80
- Locations
- 2
- Primary Endpoint
- Temperature of the core, the open wound cavity including the wound edges during major abdominal surgery
Study Overview
Brief Summary
Eighty adult patients undergoing open colon surgery will be randomized to either:
- standard warming measures including heating sheets, warming of fluids, and insulation of limbs and head, or to
- additional insufflation of humidified carbon dioxide (approx. 36-37ºC, approx. 80-100% relative humidity) via a humidifier with a heated tube (Fisher&Paykel) connected to a gas diffuser (Cardia Innovation AB) that is able to create a local atmosphere of 100% carbon dioxide (humidified ) in the open wound cavity.
PRIMARY AIM The primary aim of this study is to evaluate if humidified carbon dioxide insufflated into an open surgical wound can be used to warm the core, the open wound cavity, and the wound edges during major abdominal surgery.
SECONDARY AIMS Secondary aims are to evaluate possible differences between the groups regarding complications and clinical differences including histological signs of desiccation injury of peritoneal samples, time to extubation, core temperature after surgery, ICU stay, bleeding volume, hospital stay, postoperative pain, infections, shivering, postoperative signs of restored bowel function including bowel movements, flatus, and first meal.
Detailed Description
Eighty patients undergoing open colon surgery will be randomized to either standard warming measures including heating sheets, warming of fluids, and insulation of limbs and head or to additional insufflation of humidified carbon dioxide (approx. 36-37ºC, approx. 80-100% relative humidity) via a humidifier with a heated tube (Fisher&Paykel) connected to a gas diffuser (Cardia Innovation AB) that is able to create a local atmosphere of 100% carbon dioxide (humidified) in the wound cavity.
Wound temperatures will be measured every 10 minutes with an infra-red camera positioned approximately 1m above the wound with a camera support. Wound areas and wound edges of stored images will be delineated with a soft ware program. Peritoneal samples (3x3x1mm) will be taken at start of the operation, after 30 minutes and before closure of the abdomen. The samples will immediately be stored in RNA-later solution, and deep frozen for later analysis of epithelial (peritoneal) and endothelial function/tissue damage.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Factorial
- Primary Purpose
- Treatment
- Masking
- Single (Participant)
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- •major open abdominal surgery (colon surgery) in adults
- •patient signed informed consent
Exclusion Criteria
- •acute surgery
Outcomes
Primary Outcomes
Temperature of the core, the open wound cavity including the wound edges during major abdominal surgery
Time Frame: duration surgery up to 12 hours
Secondary Outcomes
- Time to extubation(up to 30 days after surgery)
- Histological signs of dessication injury of peritoneal samples(duration surgery up to 12 hours)
- ICU stay(up to 30 days after surgery)
- Pain and need of analgesia(up to 30 days after surgery)
- Restoration of bowel function after surgery including flatus, bowel movements, and first meal(up to 30 days after surgery)
- Postoperative infections including pneumonia and surgical site infection(up to 30 days after surgery)
- Postoperative shivering(up to 24 hours after surgery)
- Suture removal(up to 30 days after surgery)