Preventive Therapy of Postoperative Intra-abdominal Infection Based on Serum Lactate Changes

Sponsor
Peking Union Medical College Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05052619
Collaborator
(none)
297
1
2
60
5

Study Details

Study Description

Brief Summary

Intra-abdominal infection is one of the most serious complications after pancreatic resection. The preventive use of antibiotics intraoperatively could reduce the incidence rate of postoperative intra-abdominal infection. According to the previous retrospective study, changes of serum lactate level on postoperative day1 could predict the incidence rate of postoperative intra-abdominal infection. This prospective RCT is to further validate and promote the findings and conclusion.

Condition or Disease Intervention/Treatment Phase
  • Drug: Preventive use of advanced antibiotics
  • Other: Routine
N/A

Detailed Description

Postoperative intra-abdominal infection is one of the most serious complications after pancreatic resection. Once diagnosed as postoperative intra-abdominal infection, the patient would not only suffer a lot, but also spend much more money and time in hospital. Moreover, subsequent sepsis and septic shock would imperil the patient's life. The preventive use of antibiotics intraoperatively is the key to prevent this complication, but the time, dosage, and choice of the antibiotics are worth discussing. According to the previous work, the investigators found the changes in serum lactate level on postoperative day (POD) 1 could predict postoperative intra-abdominal infection one week before it really happened. The cutoff level of lactate is 3.25mmol/L. Thus, the investigators recommend preventive use of advanced antibiotics for patients who have a peak serum lactate level of >3.250 mmol/L in 24h after pancreatic resection (doi: 10.1007/s00268-021-05987-8. PMID: 33604712).

The investigators would verify the finding in this randomized controlled trial. Patients with peak lactate level >3.250 mmol/L in POD1 and met other inclusion criteria would be recruited and separated into "preventive use of advanced antibiotics group" (experimental group) and "routine group" (control group) randomly. Patients in experimental group would be treated with advanced antibiotics to avoid postoperative intra-abdominal infection. Patients in control group would be treated with routine method (antibiotics with lower levels). To compare the incidence rate of infection and other complications, as well as the payment and other index, the investigators would see if the patients in experimental group could have better prognosis after pancreatic surgery.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
297 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Care Provider)
Primary Purpose:
Prevention
Official Title:
A Prospective, Randomized Clinical Trial to Treat Intra-abdominal Infection Preventively After Pancreatic Surgery Based on Serum Lactate Changes
Actual Study Start Date :
Jul 1, 2021
Anticipated Primary Completion Date :
Jul 1, 2023
Anticipated Study Completion Date :
Jul 1, 2026

Arms and Interventions

Arm Intervention/Treatment
Experimental: Preventive use of advanced antibiotics group

Treat patients in this group with advanced preventive usage of antibiocs: Sulperazon 3g q8h, in postoperative days 1-5.

Drug: Preventive use of advanced antibiotics
Treat patients in this group with advanced preventive usage of antibiocs: Sulperazon 3g q8h, in postoperative days 1-5.
Other Names:
  • Sulperazon
  • Other: Routine group

    Treat patients in this group with routine preventive usage of antibiocs: Cefmetazole 1g q12h, in postoperative days 1-3.

    Other: Routine
    Treat patients in this group with routine preventive usage of antibiocs: Cefmetazole 1g q12h, in postoperative days 1-3.
    Other Names:
  • Cefmetazole
  • Outcome Measures

    Primary Outcome Measures

    1. Incidence rate of postoperative intra-abdominal infection [in 30 days after surgery]

      The incidence rate of postoperative intra-abdominal infection is expected to be lower in experimental group than control group

    Secondary Outcome Measures

    1. The amount of white blood cell [postoperative days 1, 3, 5, 7, 14, 21, 28]

      It is expected to be lower in experimental group than in control group

    2. The level of procalcitonin [postoperative days 1, 3, 5, 7, 14, 21, 28]

      It is expected to be lower in experimental group than in control group

    3. The level of C-reactive protein [postoperative days 1, 3, 5, 7, 14, 21, 28]

      It is expected to be lower in experimental group than in control group

    4. The level of interleukin [postoperative days 1, 3, 5, 7, 14, 21, 28]

      It is expected to be lower in experimental group than in control group

    5. The level of tumor necrosis factor α [postoperative days 1, 3, 5, 7, 14, 21, 28]

      It is expected to be lower in experimental group than in control group

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. treatment by pancreatic resection, including pancreaticoduodenectomy, pancreatosplenectomy, total pancreatectomy, and other variant operations;

    2. revival in the intensive care unit (ICU) with standard serum lactate elution treatments after surgery instead of the operation room or general ward;

    3. availability of complete preoperative, intraoperative, and postoperative data;

    4. the peak serum lactate level in 24 hours after surgery >3.250 mmol/L.

    Exclusion Criteria:
    1. a history of surgical treatment of any upper abdominal lesions before the current hospital admission;

    2. the minimum mean arterial pressure <65 mmHg during the operation;

    3. without written informed consents for the perioperative situation and related studies.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Peking Union Medical College Hospital Beijing Beijing China 100730

    Sponsors and Collaborators

    • Peking Union Medical College Hospital

    Investigators

    • Study Director: Yatong Li, MD, Peking Union Medical College Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    Peking Union Medical College Hospital
    ClinicalTrials.gov Identifier:
    NCT05052619
    Other Study ID Numbers:
    • Lac-infection
    First Posted:
    Sep 22, 2021
    Last Update Posted:
    Sep 27, 2021
    Last Verified:
    Sep 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Keywords provided by Peking Union Medical College Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 27, 2021