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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT06148597
Other study ID # 2023/04-4
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date October 20, 2023
Est. completion date May 20, 2024

Study information

Verified date January 2024
Source Zonguldak Bulent Ecevit University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Adequate postoperative analgesia is difficult to achieve in patients undergoing laparoscopic sleeve gastrectomy (LSG). Epidural anesthesia is technically difficult due to subcutaneous fat, which increases the risk of serious complications. Moreover, patients in this condition often have comorbidities that require anticoagulation therapy. Although ultrasound-guided Transversus Abdominis Plane (TAP) block may be useful, it is still controversial. Recently, modified thoracoabdominal nerve block via perichondrial approach (M-TAPA) has been reported as a new and promising technique that provides effective analgesia in the anterior and lateral thoracoabdominal wall. The most common reason for hospitalization after laparoscopic surgery is pain after nausea and vomiting. In addition, superficial and tachypneic breathing resulting from the patient's inability to breathe deeply with pain causes closure of small airways and increase in intrapulmonary shunts, resulting in hypoxia. Postoperative pain management is important not only to prevent pain but also to reduce pulmonary complications that may occur due to changes in lung function and to reduce mortality and morbidity by controlling the stress response. In this study, The investigators investigated the effect of modified thoracoabdominal nerve block via perichondrial approach (M-TAPA) on pulmonary function in patients undergoing laparoscopic bariatric surgery under general anesthesia.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 1
Est. completion date May 20, 2024
Est. primary completion date April 20, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Between 18-65 years old - ASA I-II-III risk group - Patients whose approval was obtained through an informed consent form - Will undergo laparoscopic bariatric surgery - Patients who will cooperate for the PFT test Exclusion Criteria: - <18 years and >65 years - ASA = IV - 50% below the expected value in SFT - Known diaphragmatic paralysis - Having had a myocardial infarction within 1 month - Dementia or confusion - Lack of cooperation - Those with respiratory disease - Congestive heart failure - Unstable hypertension - Had thoracoabdominal surgery

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Modified thoracoabdominal nerves block through perichondrial approach (M-TAPA)
application local anesthetic between internal oblique and transversus abdominis muscle at the level of 10th costal cartilage

Locations

Country Name City State
Turkey Zonguldak Bülent Ecevit University Medicine Faculty Zonguldak Kozlu

Sponsors (1)

Lead Sponsor Collaborator
Zonguldak Bulent Ecevit University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary FEV1/FVC ratio Pulmonary function during the procedure
Secondary Numerical Rating Scale pain assessment tool (minimum: 0, maximum: 10) during the procedure
Secondary opioid consumption need of opioid postoperatively 24 hours after surgery
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