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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03719157
Other study ID # 1
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 1, 2019
Est. completion date October 1, 2019

Study information

Verified date January 2021
Source Diskapi Yildirim Beyazit Education and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Main purpose of this prospective single center randomized study is to compare the analgesic effect of ultrasound guided Unilateral Oblique Subcostal Transversus Abdominis Plane (TAP),unilateral Erector Spinae Plane (ESP) blocks and Port site infiltration of local anesthetic in subjects undergoing laparoscopic cholecystectomy. Total 100 patients, American society of anaesthesiology physical status I-II aged between 18-65 who underwent laparoscopic cholecystectomy will recruit to the study.


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date October 1, 2019
Est. primary completion date September 1, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - ASA Status 1-2 patients Exclusion criteria - Patients with a body mass index (BMI) of >40kg/m2 - ASA score of >III - Previous abdominal surgery - Pregnant or breastfeeding patients - Patients with coagulopathy - Known local anesthetic allergy - infection at the injection site

Study Design


Intervention

Procedure:
Unilateral ESP Block
USG guided ESP block will perform unilateral with Bupivacaine and Lidocain mixture
Unilateral OSTAP Block
USG guided OSTAP block will perform unilateral with Bupivacaine and Lidocain mixture
Injection of Local Anesthetic to Trocar Insertion
Bupivacaine infiltration will be performed at the end of the surgical procedure to trocar insertion sites.
Drug:
intravenous patient controlled analgesia
All patients were followed using a standardized postoperative analgesia protocol which includes tramadol PCA. Tramadol at a concentration of 5 mg/mL is included in our PCA protocol (total volume 100 mL.) PCAs were set to no basal infusion and 10 mg bolus doses with a 20 min lock time.

Locations

Country Name City State
Turkey Diskapi education and research hospital Ankara

Sponsors (1)

Lead Sponsor Collaborator
Diskapi Yildirim Beyazit Education and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Postoperative opioid consumption Patient controlled analgesia (PCA) will provide with tramadol PCA. Total tramadol consumption will calculate and record till the postoperative 24th hours. 24 hours
Primary Postoperative pain scores: NRS Postoperative pain assessment will apply with numerical rating scale. These scores will record till the postoperative 24 th hours. 24 hours
Secondary postoperative nause and vomiting The patient with nausea and vomiting will be recorded. 24 hours
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