← Back to all trials
Not Yet Recruiting
NCT07721818
The Association Between Bilateral Intermediate Cervical Plexus Block and Salivary Biomarkers of Surgical Stress Response Following Total Thyroidectomy
Conditions: Surgical Stress Response, Total Thyroidectomy, Saliva Collection, Cervical Plexus Block
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: PHASE4
Enrollment: 48
Sponsor: University Hospital Dubrava
Summary
The aim of this study is to evaluate how an ultrasound-guided bilateral intermediate cervical plexus block affects the surgical stress response in individuals undergoing total thyroidectomy. The primary objective is to quantify this physiological response through the analysis of specific stress and inflammatory biomarkers collected from the participants' saliva.
The clinical trial will encompass a total of 48 patients, randomized equally into two distinct cohorts of 24 participants each. The control group will undergo standard total intravenous anesthesia (TIVA), whereas the experimental group will receive the bilateral intermediate cervical plexus block in combination with the TIVA protocol.
It is hypothesized that integrating this regional nerve block with total intravenous anesthesia will significantly attenuate the surgical stress response, evidenced by a reduction in salivary biomarker concentration, compared to utilizing TIVA alone during thyroid surgery.
Validating this hypothesis would offer robust scientific evidence to advocate for the routine integration of the bilateral intermediate cervical plexus block into standard anesthetic practices for total thyroidectomy. Ultimately, this approach aims to minimize perioperative stress and facilitate a more rapid postoperative recovery for patients.
Eligibility Criteria
Inclusion Criteria:
* ASA I or ASA II
* euthyroid status
* signed informed consent
Exclusion Criteria:
* patients who refuse to sign the informed consent form
* infection at the block injection site
* hypersensitivity or contraindications to the medication used in the study
* hypo/hyperthyroidism at the time of surgery
* presence of substernal goiter
* additional surgical interventions during the procedure
* history of previous neck surgery or radiation
* coagulopathy
* uncontroled respiratory disease
* diabetes mellitus
* autoimune disease
* chronic corticosteroid therapy
* smokers
* pregnant women
Source: ClinicalTrials.gov (NCT07721818). StuddyBuddy aggregates publicly available trial information.