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Peripheral Nerve Block clinical trials

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NCT ID: NCT04539730 Withdrawn - Opioid Use Clinical Trials

Liposomal Bupivacaine in Adductor Canal Blocks (ACB)

Start date: December 1, 2021
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate whether liposomal bupivacaine is superior to normal bupivacaine in terms of providing better pain control postoperatively after total knee arthroplasty.

NCT ID: NCT03385967 Withdrawn - Analgesia Clinical Trials

Duration of Analgesia With Dexmedetomidine and Ropivacaine in Brachial Plexus Block

Start date: April 2019
Phase: Phase 4
Study type: Interventional

This is a prospective, randomized, double blind study of adding dexmedetomidine to ropivacaine for Brachial plexus block and assessing the analgesia with VAS pain scales(0-10), Satisfaction scale by VAS scale(0-10) and time to first analgesic consumption. This study mainly aims to investigate whether addition of dexmedetomidine helps in increasing the duration of analgesia.

NCT ID: NCT01625208 Withdrawn - Clinical trials for Peripheral Nerve Block

Supraclavicular Versus Combined Block for Ulnar and Median Distribution Hand Surgery

Start date: March 2012
Phase: N/A
Study type: Interventional

This study will examine how successfully nerves are blocked or frozen for hand surgery. Traditionally, the nerves are frozen at the base of the neck, just above the clavicle or collarbone (the supraclavicular block). This is mostly successful by itself, and provides anesthesia of the entire arm. Occasionally, an additional nerve block is required further down the arm, as the supraclavicular block may have missed a segment, or it is taking too long to come on. In this study the investigators will compare the traditional technique, with a similar but lower volume supraclavicular block plus an immediate low volume block of one nerve further down the arm (the ulnar or median nerve block, depending on which digits are being operated on). The investigators will compare success rates, speed of onset, procedural comfort and length of time of weakness and numbness, plus any adverse events.