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Joint Diseases clinical trials

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NCT ID: NCT04063943 Withdrawn - Osteoarthritis Clinical Trials

Long Term Sidus PMCF

Start date: July 12, 2019
Phase: N/A
Study type: Interventional

The objectives of this study are to assess the safety and performance of the Sidus Stem-Free Shoulder Arthroplasty System in unilateral primary total shoulder arthroplasty.

NCT ID: NCT04022057 Withdrawn - Clinical trials for Anesthesia; Functional

The Impact of a Preoperative Nerve Block in Foot and Ankle Surgery on the Consumption of Sevoflurane

Start date: August 1, 2019
Phase: Phase 2/Phase 3
Study type: Interventional

Reconstructive foot and ankle surgery is performed under general anesthesia. Included in this spectrum of surgery are ankle arthroplasties, various fusions, corrective arthrodesis, and more. Pain control for after the surgery can be achieved purely with intravenous and oral pain medication or in combination with freezing of the nerves. Nerve freezing (nerve block) placed before surgery has the potential to substantially reduce the amount of inhaled anesthetic given to the patient during surgery. This can benefit the patient with being more awake and crisp more quickly after surgery. It can also reduce cost to the system. A further benefit which has received very little attention so far, is that reducing the amount of inhaled anesthetic given also lowers the environmental footprint created by the anesthetic. For the region of the foot and ankle to be fully frozen, both the sciatic nerve and the saphenous nerve must be successfully blocked. Sciatic nerve blockade is most commonly achieved by blocking the nerve in the popliteal fossa. This block is named popliteal nerve block. The investigators will examine and quantify the amount of inhaled anesthetic used for each case and will compare how the consumption is affected by whether the nerve blocks are applied before or after surgery. Patients will have two nerve block catheters (popliteal and saphenous catheter) placed under ultrasound-guidance prior to the case by an experienced and specifically trained anesthesiologist. The catheters will be loaded with a solution to which the anesthesiologist is blinded. It will either be local anesthetic or 5% dextrose (sham). The general anesthetic will be conducted according to a research protocol with anesthetic depth being the targeted endpoint. Measurements of the required MAC-Value (minimum alveolar concentration) of inhaled anesthetic will be recorded every five minutes by a study team member. At the end of the case the anesthesiologist will be unblinded to the solution. Should the patient have received sham initially, they will now receive the full dose of local anesthetic prior to being woken up.

NCT ID: NCT03840122 Withdrawn - Knee Arthropathy Clinical Trials

ACB + IPACK Block With or Without Local Infiltration in RA-TKA

Start date: October 8, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the outcomes of an Adductor canal block (ACB) + interspace between the popliteal artery and the capsule of the knee (IPACK) block along with a single intraoperative injection of a standard local anesthetic that includes Ropivacaine, Epinephrine, Ketorolac, Clonidine and saline to an ACB + IPACK block without the intraoperative injection of a standard local anesthetic in patients undergoing Robotic Arm-Assisted TKA (RA-TKA).

NCT ID: NCT03836313 Withdrawn - Opioid Use Clinical Trials

Assessing if Cryoneurolysis Improves Prehabilitation and Decreases Pain After Surgery With Less Opioid Use in TKA Patients

Start date: March 2019
Phase: N/A
Study type: Interventional

This is a prospective, randomized control trial to evaluate the impacts of preoperative cryoneurolysis treatment on opioid consumption with prehabilitation and resulting postoperative functional improvement in patients undergoing elective primary total knee arthroplasty (TKA).

NCT ID: NCT03488433 Withdrawn - Rotator Cuff Tear Clinical Trials

Abduction Brace Versus Antirotation Sling for Immobilization Following Reverse Shoulder Arthroplasty and Rotator Cuff Repair

Start date: November 1, 2019
Phase: N/A
Study type: Interventional

To compare the functional and anatomical outcomes, and patient satisfaction and compliance between two different postoperative immobilization methods - abduction shoulder brace versus simple arm sling - following 2 common shoulder surgical procedures - rotator cuff repair (RCR) and reverse total shoulder arthroplasty (RTSA) through a prospective randomized clinical trial.

NCT ID: NCT03488147 Withdrawn - Dysphagia Clinical Trials

Whether Proton Pump Inhibitors, Administered Prior to or After Surgery, Can Reduce the Incidence and/or Severity of Difficulty Swallowing Foods and/or Liquids,Following Anterior Cervical Surgery

Start date: July 2020
Phase: Phase 2
Study type: Interventional

The researchers wish to investigate whether proton pump inhibitors, administered prior to or after surgery, can reduce the incidence and/or severity of difficulty swallowing foods and/or liquids,following anterior cervical surgery.

NCT ID: NCT03472755 Withdrawn - Hip Arthropathy Clinical Trials

Comparison of Direct Anterior and Posterior Surgical Approaches in Regards to the Patient' Physical Characteristics

MOPHEM
Start date: March 23, 2018
Phase: N/A
Study type: Interventional

Recent increased interest in tissue-sparing and minimally invasive arthroplasty has given rise to a sharp increase in the utilization of direct anterior total hip arthroplasty.

NCT ID: NCT03119038 Withdrawn - Osteoarthritis Clinical Trials

Efficacy of Intraoperative Injections on Postoperative Pain Control During Total Hip Replacement

Start date: April 30, 2016
Phase: Phase 4
Study type: Interventional

The purpose of this study is to clarify the efficacy of a multidrug versus single drug periarticular injection when only standard operative and postoperative pain management protocols used and the control group is exposed to what our investigators believe is the standard of care, single medication periarticular injection

NCT ID: NCT02996942 Withdrawn - Joint Disease Clinical Trials

Key Aspects of Medical Practice in Patients With Haemophilia A

KAPPA
Start date: July 2012
Phase:
Study type: Observational [Patient Registry]

The KAPPa project has the aim to create an international database in which information about clinical features, therapeutic management, burden of illness and costs of severe and moderate haemophilia A patients from different countries and sites is collected. The aim of this project is to analyse the influence of such different characteristics on medical, psychosocial and economic outcomes in patients over the long-term.

NCT ID: NCT02668211 Withdrawn - Osteoarthritis Clinical Trials

Radiostereometric Analysis (RSA) of the PROFEMUR® Preserve Classic Femoral Components

TOPAZ
Start date: November 2016
Phase: N/A
Study type: Interventional

MicroPort Orthopedics (MPO) is conducting this study to investigate the primary stability of its PROFEMUR® Preserve Femoral Components using radiostereometric analysis (RSA). RSA allows precise measurement of micromotion around orthopedic implants and hence, may estimate long-term fixation to bone.