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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04101266
Other study ID # 59/13
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 30, 2019
Est. completion date April 1, 2020

Study information

Verified date June 2021
Source Diskapi Yildirim Beyazit Education and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

It is compared that combined suprascapular and infraclavicular nerve blocks to interscalene nerve block for clinical outcomes after shoulder surgery


Description:

In this study, the investigators planned to investigate postoperative pain, analgesic dosage, respiratory effects of the block and side effects of patients undergoing general anaesthesia after arthroscopic shoulder surgery under preoperative interscalene nerve block or suprascapular + infraclavicular nerve block.


Recruitment information / eligibility

Status Completed
Enrollment 76
Est. completion date April 1, 2020
Est. primary completion date March 1, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - Patients scheduled for elective shoulder surgery under general anesthesia with suprascapular + infraclavicular nerve block or interscalene nerve block for any reason ASA 1-3 patients Exclusion Criteria: - Diabetes - coagulopathy - local anesthetic allergy - chronic opioid users - neurological deficit of the surgical limb - obstructive or restrictive pulmoner disease - inability to understand pain scores

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Interscalene block
30 minutes before anaesthesia induction interscalene nerve block will be applied with ultrasound guidance with %0,25 bupivacain 20 cc .The sham block consisted of after patients were placed in the lateral decubitus position skin preparation, ultrasound scanning of the suprascapular region, and a dry-needling, all performed to preserve patient blinding in the ISB group patients.
suprascapular and infraclavicular nerve block
30 minutes before anaesthesia induction suprascapular with %0,25 bupivacain 10 cc .and infraclavicular nerve block with %0,25 bupivacain 10 cc will be applied with ultrasound guidance

Locations

Country Name City State
Turkey Diskapi Yildiim Beyazit Eduation and Research Hospital Ankara

Sponsors (1)

Lead Sponsor Collaborator
Diskapi Yildirim Beyazit Education and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary postoperative pain: numeric rating scale (NRS) postoperative pain will be evaluated by numeric rating scale (NRS) . postoperative 30. minute, 4. hour, 8.hour,12. hour, 24. hour, 48. hour
Secondary phrenic nerve paralysis evaluated with ultrasound Thirty minutes after the block, M-mode ultrasound examination of the ipsilateral hemidiaphragm was performed to measure diaphragmatic excursion. thirty minutes after the nerve block
See also
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Not yet recruiting NCT03602469 - Postoperative Analgesia of Magnesium Sulfate in Suprascapular Nerve Block Following Shoulder Arthroscopy N/A
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Recruiting NCT05739201 - ISB, SSNB, and PENG Block for Arthroscopic Shoulder Surgery N/A
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Completed NCT04669639 - A Comparison of ESP Block to SSN Block for Analgesia in Shoulder Surgery N/A
Active, not recruiting NCT04675671 - Analgesic and Anxiety Efficacy of Preemptive Pregabalin
Completed NCT03277326 - Interscalene vs Anterior and Posterior Suprascapular Nerve Block for Shoulder Arthroscopic Surgeries N/A
Recruiting NCT00731146 - Effects of Technique on the Local Anesthetic Dose Required for Interscalene Brachial Plexus Block N/A
Completed NCT03212443 - Combined Suprascapular and Axillary Nerve Blocks for Arthroscopic Shoulder Surgery N/A