The comparasion of comfort scale after ultrasound guided superficial cervical plexus block between lidocaine and ropivacaine

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100046038

Enrollment

Unknown

Registered

2021-05-02

Start date

2021-06-01

Completion date

Unknown

Last updated

2021-12-13

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

Conditions

Internal jugular vein catheterization

Interventions

Group 1:Perform ultrosound guided superficial cervical plexus block with lidocaine

Group 2:Perform ultrosound guided superficial cervical plexus block with ropivacaine

Group 3:Perform local anesthesia with lidocaine

Eligibility

Sex/Gender

All

Age

18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 75 years; 2. No gender limit; 3. ASA classification I-III level; 3. Capable of cooperating with tube placement operation.

Exclusion criteria

Exclusion criteria: 1. Patients who cannot communicate in normal language; 2. Patients with a history of local anesthetic allergy; 3. Patients with severe coagulopathy (platelet count6s, INR>1.4); 4. Patients who are taking analgesics or/and antidepressants; 5. Patients who have participated in other clinical studies.

Design outcomes

Primary

Measure	Time frame
Onset time of local anesthetic;Scope of anesthesia;NRS score;Bruggrmann comfort scale;	—

Secondary

Measure	Time frame
Sleep quality scale;Anxiety scale;	—

Countries

China

Contacts

Public ContactZheng Kang

Zhongda Hospital, Southeast University

13327819101@163.com+86 13327819101

Outcome results

None listed

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