The Association Between Bilateral Intermediate Cervical Plexus Block During Total Thyroidectomy and Surgical Stress Response
Recruiting
Phase 4
Interventional Study
Thyroid Cancer
Thyroid and Parathyroid Surgery
Hyperthyreosis and Goiter
Surgical Stress Response
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Trial phase
- Phase 4
- Study type
- Interventional
- Purpose
- Other
- Participants needed
- 48 (estimated)
- Sponsor
- University Hospital Dubrava · Other
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About This Trial
The aim of this study is to determine the impact of ultrasound-guided bilateral intermediate cervical plexus block on the surgical stress response in patients undergoing total thyroidectomy, as measured by the concentration of stress and inflammatory biomarkers in the participants' saliva and serum.
The study will be conducted on 48 subjects divided into two groups of 24: a control group receivin…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* patienets of both sexes
* 18 years of age and older
* 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 t…
Contacts