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The effect of different administration methods of dexamethasone on breakthrough pain after nerve block in patients with shoulder rotator cuff: A prospective study.

The effect of different administration methods of dexamethasone on breakthrough pain after nerve block in patients with shoulder rotator cuff: A prospective study.

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101832
Enrollment
Unknown
Registered
2025-04-30
Start date
2024-04-10
Completion date
Unknown
Last updated
2025-05-05

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

Conditions

The Rebound Pain

Interventions

Group IV:0.25% Ropivacaine + normal saline totaling 20ml for Brachial Plexus Block 5mg (1ml) Dexamethasone intravenous injection
Group PN:0.25% Ropivacaine + 5mg (1ml) Dexamethasone totaling 20ml for Brachial Plexus Block 1ml Normal saline intravenous injection

Sponsors

The First Affiliated Hospital of Soochow University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Signing of the informed consent form. 2. Classification I-II by the American Society of Anesthesiologists (ASA); 3. Planned elective repair surgery for shoulder cuff injury.

Exclusion criteria

Exclusion criteria: 1. Allergy to the drugs used in this study 2. Coagulation dysfunction 3. History of previous shoulder and chest surgery, or peripheral neuropathy caused by spine and upper limb diseases 4. History of long-term opioid use, or history of alcohol and drug addiction 5. Combined with severe heart, liver, kidney and other organ insufficiency 6. Diabetic patients 7. Those who cannot cooperate with the numerical rating scale (NRS) test

Design outcomes

Primary

MeasureTime frame
the incidence of rebound pain;NRS score;

Countries

China

Contacts

Public ContactCheng Hao

The First Affiliated Hospital of Soochow University

chenghao@163.com+86 139 0621 7420

Outcome results

None listed

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