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Interscalen brachial plexus blockade combined with Perineural dexamethasone for post operative analgesia after shoulder surgery

Interscalen brachial plexus blockade combined with Perineural dexamethasone for post operative analgesia after shoulder surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170423033615N3
Enrollment
60
Registered
2023-10-14
Start date
2023-09-06
Completion date
Unknown
Last updated
2023-11-13

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

Conditions

post operation pain in shoulder surgery.

Interventions

Intervention 1: Intervention group: In the intervention group,the combination of lidocaine 1.5% in the amount of 2 cc, bupivacaine 0.5% in the amount of 2 cc (20 mg), and 2 cc of dexamethasone (8 mg)

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: ASA I , ASA II Candidate for shoulder surgery No substance abuse in the past 6 weeks No orthopedic surgery in the lower limb under spinal anesthesia no respiratory diseases, diabetes; Cardiovascular no drug addiction according to definition Normal body temperature No history of shivering No history of seizures Absence of tremors or Parkinson's Not taking NSAIDs 24 hours before surgery Absence of infection or wound No Allergy to local anesthetics Not pregnant and breastfeeding Duration of surgery maximum 3 hours No allergy to Estroids

Exclusion criteria

Exclusion criteria: History of psychiatric disorders patient refusal or inability to give informed consent ASA class III and above anticoagulants History of adverse reactions to steroids History of adverse reactions to local anesthetics History of drug abuse Occurrence of complications that require intervention within 24 hours after the operation receiving blood transfusion during surgery or anesthesia central body temperature to less than 32 degrees Celsius during surgery

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: 12 hours after the operation, 24 hours after the operation. Method of measurement: VAS Score.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMahshid Ghasemi MD

Shahid Beheshti University of Medical Sciences

mahshidghasemi@sbmu.ac.ir+98212201072

Outcome results

None listed

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