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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04686890
Other study ID # KIA 2020/96
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 30, 2020
Est. completion date March 10, 2021

Study information

Verified date March 2021
Source Kocaeli University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The efficacy of erector spinae plane block versus intravenous analgesics compared relate to the morphine consumptions


Description:

Patients undergoing elective nefrectomy were enrolled. Patients divided into two groups with a sealed envelope technique to ESP+ pca morphine group or iv analgesic + pca morphine group. All patients will premedicated. then esp will applied to one group before surgery at the preoperative care unit by the same anesthesiologist. The other group will receive intravenous tramadol 1 mg/kg + NSAID 1 ampule + parol 10 mg/ kg + ondansetron 4 mg bolus. İntravenous morphine pca with a concentration of 0.5 mg/cc were applied. And administered 1 mg boluses every 15 minutes lock time and 4 hour limit as 4 mg arranged. An anesthesia nurse who is responsible of all pcas' in the hospital was recorded the variables of these patients in the service


Recruitment information / eligibility

Status Completed
Enrollment 46
Est. completion date March 10, 2021
Est. primary completion date March 10, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:18-65 years age - ASA I-II - undergoing elective nephrectomy Exclusion Criteria:- ASA>3 - heart disease - pregnancy - lung disease - scoliosis - bleeding disorder - infection at the manipulation side

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
erector spinea plane block administered preoperative open nephrectomy
erector spinae plane block applied in this group before open nephrectomy
intravenous analgesic ( 1 mg/kg tramadol + non-steroid antiinflamatuar paracetamol )drug + 10 mg.kg
intarvenous analgesic administered in this group for analgesia end of the open nephrectomy

Locations

Country Name City State
Turkey Kocaeli University Medical Faculty Kocaeli

Sponsors (1)

Lead Sponsor Collaborator
Kocaeli University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Postoperative intravenous morphine patient controlled analgesia consumption morphine consumptions were recorded till 24 th hour postoperatively during postoperatively
Primary Peroperative remifentanyl consumption Amount of Remifentanyl consumption recorded Peroperatively
Secondary Visual analog rating scores pain scores were recorded during surgery during postoperative surgery
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