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Arthroplasty Complications clinical trials

View clinical trials related to Arthroplasty Complications.

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NCT ID: NCT04691362 Completed - Clinical trials for Arthroplasty Complications

Noninferiority Oral Tranexamic Acid vs Intravenous Administration in Total Hip Arthroplasty

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

To find noninferiority relationship between oral and intravenous administration of tranexamic acid on peroperative and postoperative blood loss and serum concentration during primary total hip arthroplasty.

NCT ID: NCT04653415 Completed - Knee Osteoarthritis Clinical Trials

Large Doses of Methylprednisolone Combined With Gabapentin in Total Knee Arthroplasty

Start date: June 1, 2019
Phase: Phase 4
Study type: Interventional

The aim of the study was to assess whether administration of gabapentin and methylprednisolone as "pre-emptive analgesia" in a group of patients above 65 years of age would be effective in complex pain management therapy following total knee arthroplasty (TKA). For the study investigators will qualify one hundred seventy, above 65 years old patients. The participants will be double-blind randomized into two groups: the study and controls The study group will receive as "pre-emptive" analgesia a single dose of 300 mg oral gabapentin and 125 mg intravenous methylprednisolone, while the others placebo. Perioperatively, all the patients will receive opioid and nonopioid analgesic agents calculated for 1 kg of body weight. Investigators will measure the levels of inflammatory markers (leukocytosis, C-reactive protein - CRP), pain intensity level at rest (numerical rating scale - NRS), the life parameters and all complications.

NCT ID: NCT04653090 Completed - Osteoarthritis Clinical Trials

Varus Stem Positioning of a Cementless Anatomical THA. (VARABG)

VARABG
Start date: January 1, 2018
Phase:
Study type: Observational

Varus positioning is the most common femoral malposition in total hip arthroplasty (THA). The aim of this study was to compare the long-term results of an anatomical cementless femoral stem positioned in varus with those in neutral alignment.

NCT ID: NCT04565093 Completed - Clinical trials for Arthroplasty Complications

Efficacy of iPACK After Unilateral TKA

Start date: September 28, 2020
Phase: N/A
Study type: Interventional

Total knee arthroplasty (TKA) is a common orthopedic procedure associated with severe postoperative pain which may limit patient rehabilitation and hospital discharge. Although various analgesic techniques have been proposed, there is currently no consensus on the optimal protocol to improve functional outcomes following TKA. The ideal analgesic regimen post TKA should enable adequate pain control, early mobilization and physical therapy, shorten hospital stay, reduce the risk of postoperative complications and improve patient satisfaction. Our hypothesis is iPACK (Interspace between the Popliteal Artery and the Capsule of the posterior Knee) peripheral nerves anesthetic block is superior to Periarticular local Infiltration Analgesia (LIA)which is commonly given by the surgeons during the TKA in terms of pain relief and early mobilization.

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: NCT04520841 Recruiting - Amputation Clinical Trials

Clinical Trial Comparing Negative Pressure Wound Therapy and Standard Dry Dressings

BERLYTZ
Start date: June 1, 2020
Phase: N/A
Study type: Interventional

Negative pressure dressings are currently widely used in wound management. Their use is gradually being extended to surgical scars. However, studies demonstrating a clear benefit are rare, particularly in terms of postoperative discharge, the need for surgical revision due to prolonged oozing and cost. The aim of this study is to evaluate the benefit of such a device in post-operative revision prosthesis surgery (hip and knee), as well as lower limb amputations.

NCT ID: NCT04505748 Completed - Clinical trials for Total Knee Arthroplasty

Is Self-transfusion Safe After Total Knee Arthroplasty in Terms of Nephrotoxicity of Gentamicin From Bone Cement?

Start date: January 1, 2020
Phase: N/A
Study type: Interventional

Considering that the high local concentration of antibiotic from bone cement is delivered intravenously through the self-transfusion process, systematic toxicity has never been evaluated. In addition, the effectiveness of self-transfusion with the routine concomitant use of other modern blood-salvage strategies, like tranexamic acid, should be also assessed. Therefore we performed a randomized study to assess: 1) the safety of self-transfusion in TKA by comparing the gentamicin concentrations resulting from the use or not of autologous blood transfusion. 2) the efficacy of self-transfusion in TKA, with the concomitant administration of tranexamic acid. The serum concentration of aminoglycosides has been measured in two groups of 20 patients each, after TKA, according to the use of self-transfusion. Hemoglobin, renal function and calculated blood loss were compared at several time points between groups.

NCT ID: NCT04490304 Completed - Clinical trials for Arthroplasty Complications

The Analysis of Posterior Soft Tissue Repair Durability

Start date: September 4, 2018
Phase: N/A
Study type: Interventional

Dislocation after THA usually occurs early after surgery and some go on to disabling recurrent dislocations . The posterior surgical approach is frequently used since it provides excellent exposure of both acetabulum and femur. However, many series on primary THA have reported that dislocation is 2 to 3 times more frequent after the posterior approach as compared to other approaches . Dissatisfaction with these dislocation rates resulted in the introduction of different posterior soft tissue repair techniques. Many authors have reported statistically significant differences in dislocation rates with posterior soft tissue repair as compared to without . However, there is still a concern in the literature regarding the durability of posterior soft tissue repair. The aim of our study was to analyse THA patients with posterior soft tissue repair in terms of suture durability of two different suture materials and time of suture failure.

NCT ID: NCT04437888 Active, not recruiting - Pain, Postoperative Clinical Trials

Intraoperative Ketamine for Patients Undergoing Total Joint Arthroplasty

Start date: September 14, 2020
Phase: Early Phase 1
Study type: Interventional

Prospective randomized double blinded, placebo controlled study that will evaluate the effect of intra-operative ketamine administration on post-operative analgesic requirements and self-reported pain in patients undergoing total hip and total knee arthroplasty who demonstrate high levels of pain catastrophizing.

NCT ID: NCT04433962 Completed - Osteoarthritis, Hip Clinical Trials

Investigation of the Effects of Balance Training on Balance and Functional Status Patients With Total Hip Arthroplasty

Start date: September 1, 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the effects of balance training in patients with THA until 26 weeks postoperatively. Thirty-two patients with hip osteoarthritis who were candidates for THA were recruited to the study. Sixteen patients with THA completed the study protocol and the patients were randomized into 2 groups: conventional rehabilitation (CR, n=8) or conventional rehabilitation plus balance training (CR + BT, n=8) groups. The patients were evaluated by hand-held dynamometer, single leg stance test (SLST), Tetrax balance system, Harris hip score, lower extremity function scale, 5 times sit-to-stand test and 50 foot timed walk test preoperatively and in the 8th, 14th and 26th weeks postoperatively.