Clinical Trials Logo

Clinical Trial Summary

In this study, the investigators are going to compare the analgesia effectiveness of interscalane block and suprascapular with axillary block in shoulder arthroplasties


Clinical Trial Description

In the preoperative period, the participants will be taken to the block room. The participants will be monitored, standard sedation will be applied. The first group will be get interscalene block. The second group will be get suprascapular and axillary block. The third group patient will be get no block. Afterwards, the participants will be operated under general anesthesia. A patient-controlled analgesia device will be attached to each group of participants and their postoperative follow-up will be made. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04822610
Study type Interventional
Source Istanbul University
Contact
Status Completed
Phase N/A
Start date June 30, 2021
Completion date January 31, 2022

See also
  Status Clinical Trial Phase
Not yet recruiting NCT05965986 - Preoperative Rehabilitation and Education Program N/A
Completed NCT05020821 - Superior Trunk Block Catheter Versus Single-shot Superior Trunk Block With Intravenous Dexmedetomidine for Shoulder Arthroplasty N/A
Completed NCT05350319 - Prospective Low Dose CT for Total Shoulder Arthroplasty/Reverse Shoulder Arthroplasty
Terminated NCT03845894 - Interscalene Block With Liposomal Bupivacaine vs. Interscalene Block With Bupivacaine and Adjuvants Phase 4
Recruiting NCT05699031 - Shoulder Prosthesis Telerehab Care Trial N/A
Terminated NCT03858517 - A Post-Market Clinical Evaluation of the ReUnion TSA System
Terminated NCT03880955 - A Post-Market Clinical Evaluation of the ReUnion Reverse Shoulder Arthroplasty (RSA) System
Recruiting NCT03511586 - Total Shoulder Arthroplasty Multi-Center Registry
Completed NCT04112407 - The Effect of Pretreatment for Propionibacterium Acnes on Surgical Site Burden in Shoulder Arthroplasty N/A
Recruiting NCT03268837 - Programmed Intermittent Bolus During Continuous Interscalene Nerve Block for Shoulder Arthroplasty N/A
Active, not recruiting NCT06281574 - What Are the Determinants for RTW After SA
Completed NCT05179941 - Subscapularis Indocyanine Green Perfusion Pilot Study N/A
Completed NCT03578237 - Cryoanalgesia to Prevent Acute and Chronic Pain Following Surgery: A Randomized, Double-Masked, Sham-Controlled Study N/A
Recruiting NCT00527839 - Hospital for Special Surgery Shoulder Arthroplasty Cohort