FindTrial
Sign In

Clinical study for dexmedetomidine or cervical plexus block in patients undergoing thyroid surgery under general anesthesia

Clinical study for dexmedetomidine or cervical plexus block in patients undergoing thyroid surgery under general anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900025222
Enrollment
Unknown
Registered
2019-08-17
Start date
2019-08-17
Completion date
Unknown
Last updated
2019-08-27

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

Conditions

Pain

Interventions

Control Group:Regular treatment
Group C:Superficial cervical plexus block
Group DEX:Dextromedetomidine (DEX) be intravenously pumped

Sponsors

The Third Affiliated Hospital of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Aged 18 to 60 years old, ASA I-II, thyroid surgery due to simple thyroid adenoma (grade 1-2 goiter) or thyroid adenoma

Exclusion criteria

Exclusion criteria: Unwilling to participate or withdraw halfway;patients who underwent neck surgery;Perioperative vital organ dysfunction;Serious arrhythmias such as bradycardia and sinus syndrome;Intubation difficulty or intubation number =3 times;A history of neurologic or psychiatric disorders;Recent use of steroids or opioids or other analgesics;Contraindications for hypersensitivity to study use of drugs or for the presence of superficial cervical plexus block.

Design outcomes

Primary

MeasureTime frame
Visual analogue scale score(VAS);—

Contacts

Public ContactHei Ziqing

The Third Affiliated Hospital of Sun Yat-sen University

516270031@qq.com+86 18028614327

Outcome results

None listed

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