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Effect of dexmedetomidine combined with oxelidine on the quality of recovery after thyroidectomy

Effect of dexmedetomidine combined with oxelidine on the quality of recovery after thyroidectomy

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500098528
Enrollment
Unknown
Registered
2025-03-10
Start date
2025-03-10
Completion date
Unknown
Last updated
2025-03-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative recovery quality

Interventions

Dexmetomidine combined with oxelidine group:Dexmedetomidine 0.5µg/ (kg·h) was pumped before induction for 10min, and oxelidine 1mg was given 30min before the end of surgery
Oxelidine group:Pump the same dose of normal saline for 10min before anesthesia induction,and Oxelidine 1mg was given 30min before the end of surgery
Dexmetomidine group:Dexmedetomidine 0.5µg/ (kg·h) was pumped before induction for 10min,and the same dose of normal saline was given 30min before the end of surgery
Normal saline group:Given the same dose of normal saline

Sponsors

The Affiliated Hospital of Xuzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing thyroidectomy under elective general anesthesia; 2. Preoperative American Society of Anesthesiologists grade I ~ II; 3. Aged 25-65 years old; 4. Agree to participate in the study and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Cough, hoarseness and sore throat before operation; 2. Preoperative bradycardia or atrioventricular block; 3. Operation time 3h; 4. Long-term use of opioids; 5. History of thyroid surgery; 6. Complicated with pregnancy, mental disorders, respiratory depression, severe heart, brain and lung diseases, liver and kidney failure; 7. Known or suspected gastrointestinal obstruction; 8. Other contraindications of surgery or anesthesia; 9. Inclusion of other interventional studies.

Design outcomes

Primary

MeasureTime frame
Postoperative recovery quality score;

Secondary

MeasureTime frame
Postoperative recovery quality score;Incidence of sore throat 24 hours after surgery;pain score;The incidence of bradycardia, hypotension, arrhythmia and PACU hypoxemia during operation;;Postoperative recovery time of spontaneous respiration, recovery time, extubation time, PACU resident time;Fatigue score;Postoperative adverse reactions (fever, bradycardia, tachycardia, hypertension, hypotension, dizziness, respiratory depression, dry mouth, nausea, vomiting, pain, etc.).;Length of postoperative hospital stay;

Countries

China

Contacts

Public ContactQin Yin

The Affiliated Hospital of Xuzhou Medical University

810780794@qq.com+86 138 1444 6826

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026