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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04130945
Other study ID # cost effectiveness
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 11, 2019
Est. completion date November 30, 2019

Study information

Verified date June 2020
Source Kirikkale University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Use of erector spina plane (ESP) block for postoperative analgesia is continuously increasing. However, few studies have investigated intraoperative effects of ESP block. The investigators aim to study the effects of ESP block in terms of cost-effectiveness, consumption of inhalation agents and opioids in perioperative and postoperative period.


Description:

Erector spina plane (ESP) block has analgesic efficiency and its popularity is growing steadily. ESP block forms a sensorial block by local anesthetic infiltration between the musculus erector spina and facia. ESP block given to participants undergoing laparoscopic cholecystectomy for postoperative opioid analgesia resulted in a decrease of postoperative pain scores in the first 24 h. Due to increases in health expenditure, cost control is becoming more and more important. Cost-effective studies are important in healthcare economics. Inhaled anesthetics used in anesthesia departments account for about 20% of total anesthetic agents. Local anesthetic agents decrease the minimum alveolar concentration (MAC) value of inhaled agents. And also in perioperative and post operative period, the anesthetic management often need to be supported with opioid drugs. The investigators think that ESP block has analgesic effects and decreases the consumption of inhalation agents. The investigators aim to investigate the cost-effectiveness of ESP block in anesthetic applications in laparoscopic procedures.


Recruitment information / eligibility

Status Completed
Enrollment 81
Est. completion date November 30, 2019
Est. primary completion date November 30, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

1. American Society of Anesthesiologist (ASA) physical status I-II,

2. ages 18-75 years,

3. undergoing laparoscopic cholecystectomy

Exclusion Criteria:

1. Patients with cardiac, endocrinological, neurological diseases,

2. patients with coagulation disorders

3. allergy to local anesthetics

4. Operations that started as laparoscopy but transitioned to open surgery for a surgical reason

Study Design


Related Conditions & MeSH terms


Intervention

Other:
erector spina plane block, cost analysis
in preopererative period, ESP block is going to utilise for postoperative analgesia for patients who undergo laparoscopic procedure and cost analysis will make after the end of 24 hour of operation

Locations

Country Name City State
Turkey Kirikkale Univercity Faculty of Medicine Hospital Kirikkale

Sponsors (1)

Lead Sponsor Collaborator
Kirikkale University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary the formula of consumption of inhaled agent the formula which includes fresh gas flow, valume of inhaled agent vapor, sevoflurane concentration 30 minute after the operation
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