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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05614921
Other study ID # atauniobesity
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 15, 2022
Est. completion date May 15, 2023

Study information

Verified date May 2023
Source Ataturk University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The morbidity and mortality associated with being overweight or obese have been known to the medical profession since Hippocrates, more than 2500 years ago. Pain that develops following bariatric surgery may prolong recovery time. Most morbidly obese patients have obstructive sleep apnea and cardiac comorbidities. In these patients, prolonged postoperative pain may cause early ambulation and delay performing deep breathing exercises. Using regional anesthetic techniques results in less opioid use and better pain management. External oblique internal costal block; It is a new block that provides dermatomal sensory blockage involving T6-T10 in the anterior axillary line and T6-T9 in the midline. It can be used as part of multimodal analgesia in laparoscopic cases. There is no study in the literature regarding the use of external oblique plane block in bariatric surgery yet.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date May 15, 2023
Est. primary completion date April 1, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - American Society of Anesthesiologist's physiologic state I-III patients - Laparoscopic Obesity surgery Exclusion Criteria: - Chronic pain bleeding disorders renal or hepatic insufficiency patients on chronic non-steroidal anti-inflammatory medications emergency cases

Study Design


Related Conditions & MeSH terms


Intervention

Other:
ultrasound guided external oblique intercostal plane block
ultrasound guided external oblique intercostal plane block 30 ml local anesthetic each side
Wound infiltration
5 ml local anesthetic for each trocar side

Locations

Country Name City State
Turkey Atatürk University Erzurum

Sponsors (3)

Lead Sponsor Collaborator
Ataturk University Bursa City Hospital, Erzurum City Hospital

Country where clinical trial is conducted

Turkey, 

References & Publications (2)

Cosarcan SK, Yavuz Y, Dogan AT, Ercelen O. Can Postoperative Pain Be Prevented in Bariatric Surgery? Efficacy and Usability of Fascial Plane Blocks: a Retrospective Clinical Study. Obes Surg. 2022 Sep;32(9):2921-2929. doi: 10.1007/s11695-022-06184-9. Epub 2022 Jul 1. — View Citation

White L, Ji A. External oblique intercostal plane block for upper abdominal surgery: use in obese patients. Br J Anaesth. 2022 May;128(5):e295-e297. doi: 10.1016/j.bja.2022.02.011. Epub 2022 Mar 3. No abstract available. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Postoperative opioid consumption First 24 hours total fentanyl consumption with patient controlled analgesia first 24 hours
Secondary Visual analog pain score Post operative pain will be evaluated with a Visual Analogue Scale (VAS) score of 0-10 (0= no pain and 10= worst imaginable pain) postextubation 0-24 hours
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