Clinical trial

Direct Resuscitation of the Open Peritoneum: A Randomized Controlled Trial in Non-Traumatic Patients

Name
SH Ahmeti DROP Study
Description
The DROP trial evaluates two ways of treating patients whose abdomens are left open after their abdominal surgery. The current standard of care at Sanford is for patients to have their wound covered with a sterile dressing connected to a vacuum with suction, which removes fluid from the abdomen. In this trial, we are evaluating the benefits of adding dialysis fluid to the abdomen periodically, prior to suctioning it out with the vacuum system. This trial will show if the addition of this fluid lowers the risk of complications and death, and allows the surgeon to close the abdomen sooner
Trial arms
Trial start
2021-05-14
Estimated PCD
2025-05-30
Trial end
2026-05-30
Treatment
Abthera™ Open Abdomen Negative Pressure Therapy Device System
Suction set at -125mmHg
Arms:
Negative Wound Pressure Therapy, Negative Wound Pressure Therapy with Direct Peritoneal Resuscitation
Dianeal PD-2 with 2.5% Dextrose
800mL to 1000mL of Dianeal PD-2 into Abthera™ and dwell for 1 hour.
Arms:
Negative Wound Pressure Therapy with Direct Peritoneal Resuscitation
Size
200
Primary endpoint
Major Complications
Through study completion, an average of 6 months
Number of operations and time to closure
up to 4 weeks
Eligibility criteria
Inclusion Criteria: * ≥18 years of age * Have index operation performed by one of the Trauma and Acute Care surgeons at Sanford Medical Center Fargo * Require an open abdomen due to a non-traumatic cause and placement of an Abthera™ wound vacuum * Cognitively impaired adults will be included if a Legally Authorized Representative is available to provide informed consent. Exclusion Criteria: * Patients under the age of 18 * Vulnerable populations such as pregnant women and prisoners * Patients with open abdomens as the result of trauma * Non-English speaking (Due to time constraints pre-operatively and the length of time necessary to secure translation services, non-English speaking patients will not be enrolled).
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['NA'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 200, 'type': 'ESTIMATED'}}
Updated at
2024-01-19

1 organization

1 product

4 indications

Organization
Sanford Health
Indication
Wound
Indication
Abdomen
Indication
Acute
Indication
Surgical Wound