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Not yet recruiting NCT07547124

Postoperative Analgesia and Recovery Quality in Total Thyroidectomy

Conditions: Postoperative Pain

Sponsor: Istinye University

trial.available_in: БГ
Overview
This prospective observational study evaluates the association between postoperative analgesic approaches and recovery outcomes in patients undergoing elective total thyroidectomy. Patients will be followed under routine clinical care without intervention or randomization. The primary outcome is the Quality of Recovery-15 (QoR-15) score at 24 hours. Secondary outcomes include swallowing pain, resting pain, opioid consumption, postoperative nausea and vomiting, and additional analgesic requirement.
Who can participate
Inclusion Criteria: * Patients aged 18-75 years * ASA physical status classification I-III * Patients scheduled for elective bilateral total thyroidectomy * Patients undergoing surgery under general anesthesia * Individuals able to read and understand Turkish and cognitively capable of completing the QoR-15 questionnaire * Patients providing written informed consent to participate in the study Exclusion Criteria: * Chronic opioid use (≥3 months of regular opioid use) * Presence of chronic pain syndrome * Psychiatric illness or cognitive impairment * History of neurological disease (stroke, dementia, Parkinson's disease, etc.) * Known allergy to local anesthetic agents * Previous surgical interventions in the cervical region (including revision thyroid surgery) * Planned extended surgery with concomitant neck dissection * Substernal/retrosternal goiter cases (with potential need for sternotomy or additional procedures) * Emergency surgical procedures * Patients with ASA physical status IV or higher * Pregnancy * Patients expected to require postoperative intensive care * Patients experiencing intraoperative complications that deviate from the standard monitoring protocol
Interventions
Cervical Plexus Block
OTHER
Locations 1
Turkey (1)
Istinye Üniversity
Istanbul , Merkez Mahallesi
Technical details
Status
Not yet recruiting
Study type
OBSERVATIONAL
Sex
Male and female
Minimum age
18 Years
Maximum age
65 Years
Healthy volunteers
No
Start date
10.04.2026
Completion date
10.09.2026
Registry ID
NCT07547124
Source
clinicaltrials.gov
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