Intra-abdominal Hypertension
Conditions
Brief summary
This study is a randomized, double-blinded, controlled design. In this study, Cisatracurium Besylate was selected for treatment in Intra-abdominal hypertension or abdominal compartment syndrome,accompanied with evaluating the effects on the duration of organ failure,length of hospital stay and mortality.To clarify the effect of Cisatracurium Besylate on IAH/ACS is of great significance to the clinical applications.
Detailed description
1. Title: Title: Efficacy and Safety Profile of Cisatracurium Besylate on Intra-abdominal hypertension: A Randomized Clinical Trial 2. Research center: single center 3. Design of the research: A randomized, double-blind and parallel controlled study 4. Object of the research: The patients over 18 years that Intra-abdominal pressure over 12mmHg. 5. Sample size of the research: A total of 80patients,40 cases in each group 6. Interventions: Participants in the test group received Cisatracurium Besylate 0.12mg/kg/hr continuous infusion during intubation.while participants in the control group was the same as the test group except for received the same volume of saline instead of Cisatracurium Besylate.TOF-Watch was used to monitor the function of nerve and muscle in two groups and the dose was adjusted according to the TOF value. 7. The aim of the research:To investigate the effect of Cisatracurium Besylate on IIntra-abdominal hypertension or abdominal compartment syndrome. 8. Outcome #Primary outcomes: mortality. Secondary outcomes: Duration of organ failure; Time for enteral nutrition to reach the standard (30kcal/kg); Mechanical ventilation time; Length of hospital stay 9. The estimated duration of the study#1-2years
Interventions
Participants in the test group received Cisatracurium Besylate 0.12mg/kg/hr continuous infusion during intubation。
DRUGsaline 0.12ml/kg/hr
saline 0.12ml/kg/hr
Sponsors
Tianjin Nankai Hospital
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No
Inclusion criteria
1. Intra-abdominal pressure≥12mmHg 2. Age ≥18 years old 3. Obtain informed consent.
Exclusion criteria
1. Pregnancy pancreatitis 2. Patients who have undergone percutaneous puncture or surgical drainage before admission, and have undergone surgical decompression due to early abdominal hypertension 3. Patients with a history of chronic organ dysfunction (such as uremia, COPD, liver cirrhosis, heart failure, etc.) 4. Those who refuse to participate in the research
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| All-cause 28-day mortality | 1-2year | All reasons (such as infection, hemorrhage) caused the mortality during the first 28 days after treatments |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Duration of organ failure | an average of 1-2 year | The time of organ failure recovered |
| Duration of mechanical ventilation in patients with endotracheal intubation in ICU | an average of 1 year | Duration of mechanical ventilation in patients with endotracheal intubation in ICU |
| Length of stay in hospital | 24 months | ICU stay time and hospitalization time |
Contacts
Primary ContactYa Wu
Outcome results
None listed