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Comparison of the effects of dexmedetomidine with different administration methods in ultrasound-guided cervical nerve pathway blocking

Comparison of the effects of dexmedetomidine with different administration methods in ultrasound-guided cervical nerve pathway blocking

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000031264
Enrollment
Unknown
Registered
2020-03-26
Start date
2020-03-25
Completion date
Unknown
Last updated
2021-06-07

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

Conditions

Thyroid tumor

Interventions

Con group:ropivacaine was used in cervical nerve pathway blocking
D1 group:dexmedetomidine as an adjuvant to cervical nerve pathway blocking
D2 group:cervical nerve pathway blocking combined with intravenous administration of dexmedetomidine

Sponsors

The First Affiliated Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients willing to sign informed consent; 2. 18-65 years old; 3. ASA class I-III; 4. Patients who will undergo selective thyroidectomy.

Exclusion criteria

Exclusion criteria: 1. With coagulation dysfunction; 2. Patients with infection at the puncture site; 3. Patients allergic to the study drug; 4. Analgesic drug addicts; 5. Heat rate < 50 beats/minutes or II-III Atrioventricular block; 6. With chronic pain, mental or nervous system disease; 7. With serious disease of heart head blood-vessel, liver and kidney function.

Design outcomes

Primary

MeasureTime frame
VAS scale;

Secondary

MeasureTime frame
The first time of analgesics added at the ward;Complications such as somnolence, sinus bradycardia, nausea, vomiting, hoarseness, sore throat.;

Countries

China

Contacts

Public ContactYuanhai Li

The First Affiliated Hospital of Anhui Medical University

liyuanhai-1@163.com+86 13505697561

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 9, 2026