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Cytokines of Patients With Transversus Abdominis Plane Block After Laparoscopic Colonic Surgery

Phase 4
Completed
Conditions
Laparoscopic Colonic Surgery
Interventions
Drug: transversus abdominis plane block
Registration Number
NCT02219542
Lead Sponsor
China Medical University, China
Brief Summary

The investigators designed a study to determine whether with combined general-transversus abdominis plane block anesthesia or standard general anaesthetic would provide same level of cytokines in patients undergoing Laparoscopic Colonic Surgery.

Detailed Description

The investigators designed a study to determine whether combined general-transversus abdominis plane block anesthesia or standard general anaesthetic would provide same level of cytokine in patients undergoing Laparoscopic Colonic Surgery.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
80
Inclusion Criteria
  • •Participants were deemed eligible if they were candidates for spinal anesthesia undergoing Laparoscopic Colonic Surgery
Exclusion Criteria
  • •Existing cognitive impairment as evidenced by Mini-Mental State Examination scores below 24 (of the 30 possible points)

    • A history of neurological and psychiatric diseases including stroke, and psychosis
    • Severe visual or hearing impairment
    • Unwillingness to comply with the protocol or procedures

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
a standard general anesthesiatransversus abdominis plane blocka standard general anesthesia and with transversus abdominis plane block 20 ml 0.9% sodium chloride
transversus abdominis plane blocktransversus abdominis plane blocka standard general anesthesia with transversus abdominis plane block 20 mL 0.25% ropivacaine
Primary Outcome Measures
NameTimeMethod
The change of cytokine level in plasma samplesjust after anesthesia induction ; at the end of the surgery; 24h after surgery

The blood samples were collected before induction of anesthesia and at the end of surgery.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

the First Hospital of China Medical University

🇨🇳

Shenyang, Liaoning, China

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