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Interscalene block with & without superficial cervical block

Efficacy comparison between interscalene block with & without superficial cervical block for anesthesia in clavicle surgery

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20230204057318N1
Enrollment
120
Registered
2023-02-19
Start date
2023-03-21
Completion date
Unknown
Last updated
2023-03-13

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

Conditions

Clavicle fracture surgery. Fracture of clavicle

Interventions

Intervention 1: Intervention group: After placing the patient in a suitable position, the interscalene block will be performed by experienced anesthesiologists, all of whom are trained in regional ane

Sponsors

Shahid Beheshti University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients weights less than 80 kg Age between 18 to 60 years Normal neuromotor and sensory functions Consent to the operation and performing the anesthetic procedure

Exclusion criteria

Exclusion criteria: Persistent treatment or abuse of narcotics, alcohol or other addictive drugs Contraindications of nerve blocks (Local infection, coagulopathy and sensitivity to anesthetics) Presence of mental disorders, restrictive or obstructive pulmonary diseases Pregnancy Consuming beta blockers or heart rate below 50

Design outcomes

Primary

MeasureTime frame
Need to induce general anesthesia for surgery. Timepoint: During surgery. Method of measurement: Questionnaire.

Secondary

MeasureTime frame
Postoperative pain score in the recovery room. Timepoint: From the entrance to the recovery room until discharge time from the recovery room. Method of measurement: Visual analogue scale.;The onset of sensory block. Timepoint: From the end of the nerve block procedure until the beginning of surgery. Method of measurement: Chronometer (Minute).;The amount of narcotics used in recovery room. Timepoint: From the entrance to the recovery room until discharge time from the recovery room. Method of measurement: Observation.;Need for sedation during surgery. Timepoint: During surgery. Method of measurement: Observation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAfsaneh Habibi

Shahid Beheshti University of Medical Sciences

a.habibi85@gmail.com+98 21 2990 8040

Outcome results

None listed

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