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Effect of interscalene brachial plexus block with dexmedetomidine and ropivacaine on postoperative analgesia in patient undergoing arthroscopic shoulder surgery

Effect of interscalene brachial plexus block with dexmedetomidine and ropivacaine on postoperative analgesia in patient undergoing arthroscopic shoulder surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100046470
Enrollment
Unknown
Registered
2021-05-16
Start date
2021-06-01
Completion date
Unknown
Last updated
2022-01-04

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

Conditions

should diseases

Interventions

Group R:ropivacaine for brachial plexus nerve block
Group DR:dexmedetomidine added to ropivacaine for brachial plexus nerve bloc

Sponsors

The First People's Hospital of Lianyungang
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Elective shoulder arthroscopic surgery; 2. American Association of Anesthesiologists (ASA) patient classification I~II; 3. Aged 18 to 65 years, regardless of gender; 4. Written consent was obtained after informing the participants about the nature, scope and risks related to the study.

Exclusion criteria

Exclusion criteria: 1. Refused to accept brachial plexus block; 2. BMI > 30Kg/m2; 3. History of severe cardiopulmonary disease, liver and kidney failure, and uncontrolled diabetes; 4. Allergic to any of the study drug; 5. Contraindications to brachial plexus block (coagulopathy or local infection).

Design outcomes

Primary

MeasureTime frame
duration of postoperative analgesia;

Secondary

MeasureTime frame
VAS;frequency of PCA pressed;24h total sufentanil consumption;first time of PCA pressed;patient satisfaction for the quality of analgesia;

Countries

China

Contacts

Public ContactLuan Hengfei

The First People's Hospital of Lianyungang

luanhengfei1027@163.com+86 18961325313

Outcome results

None listed

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