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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05796778
Other study ID # 685/2023
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date April 1, 2023
Est. completion date December 1, 2023

Study information

Verified date October 2023
Source Minia University
Contact hassan m. hetta, lecturer
Phone 1010901114
Email hassan.hetta@mu.edu.eg
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Shoulder surgery can be very painful surgery after which the use of opioids is often required. The well-known side-effects of opioids (e.g. respiratory depression, somnolence, nausea, vomiting, and pruritus) limit their use in so called 'fast track' surgery and anaesthesia programmes. the study aimed to compare the effect of sub omohyoid suprascapular nerve block versus interscalene nerve block in preventing postoperative pain and decreasing analgesic consumption in patients scheduled for shoulder surgery


Recruitment information / eligibility

Status Recruiting
Enrollment 72
Est. completion date December 1, 2023
Est. primary completion date November 1, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: 1. Aged 18-60 years. 2. ASA I-II. 3. Both sexes. 4. Shoulder surgery. Exclusion Criteria: 1. Patient refusal 2. Allergy to local anesthetics 3. BMI >40 kg/m2 4. Bleeding diathesis or history of anticoagulant use. 5. Psychiatric diseases. 6. Infection of the skin at the site of needle punctures area.

Study Design


Intervention

Procedure:
subomohyoid plane block
The block needle was inserted in line with the probe in a lateral-to-medial orientation toward the suprascapular nerve. Local anesthetic solution was then injected after negative aspiration for blood to achieve circumferential spread around the neurovascular bundle
Interscalene brachial plexus block
The block needle is usually advanced in plane in a lateral-to-medial direction through the middle scalene muscle to contact the nerve roots and inject local anesthetic around them.

Locations

Country Name City State
Egypt Minia University Hospital Minya

Sponsors (1)

Lead Sponsor Collaborator
Minia University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Visual analogue pain score pain score from 0 to 10 which mean 0 no pain and 10 the worst pain ever 24 hour
Secondary Time of first analgesic request the time of first demand rescue analgesia 24 hour
Secondary Total analgesic consumption total fentanyl demand 24 hour
Secondary Incidence of any side effects oxygen desaturation, pneumothorax, dyspnea, and phrenic nerve palsy, block, and opioid-related side effects 24 hour
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