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Effect of different infusion methods of dexmedetomidine on the incidence of rebound pain after shoulder arthroscopic surgery in patients with catastrophic preoperative pain

Effect of different infusion methods of dexmedetomidine on the incidence of rebound pain after shoulder arthroscopic surgery in patients with catastrophic preoperative pain

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200067064
Enrollment
Unknown
Registered
2022-12-26
Start date
2022-12-12
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Shoulder sleeve damage

Interventions

Experimental group:Dextrmedetomidine as an Adjuvant of Local Anesthesia for Nerve Block
control group:Dextrmedetomidine intravenous injection

Sponsors

Xuzhou Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. The patients who need shoulder surgery at a selected time are 18-65 years old, and ASA (American Association of Anesthesiologists Classification) I-II. 2. Pain Catastrophe Scale score>26 and Neuropathic Pain Assessment Scale DN4<4. 3. Day surgery patients discharged within the second day of surgery.

Exclusion criteria

Exclusion criteria: 1. Patients with PCS score = 26; 2. Patients with DN4 = 4 points; 3. Patients who refused to participate in the experiment, patients who were allergic to various drugs in the experiment, patients with chronic peripheral neuropathy, patients with puncture point infection, and patients who refused or could not understand the questionnaire.

Design outcomes

Primary

MeasureTime frame
Occurrence rate of rebound pain;

Secondary

MeasureTime frame
Postoperative NRS score;Athens Insomnia Scale;Sensory recovery time;Motion recovery time;

Countries

China

Contacts

Public ContactHUAN XIANG

Xuzhou Central Hospital

120895745@QQ.COM+86 18952111208

Outcome results

None listed

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