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Orthopedic Disorder clinical trials

View clinical trials related to Orthopedic Disorder.

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NCT ID: NCT05552599 Completed - Hypothermia Clinical Trials

Body Temperature Changes and Early Postoperatıve Pressure Sore

Start date: March 3, 2018
Phase: N/A
Study type: Interventional

This study aims to determine effect of body temperature changes during total knee arthroplasty surgery on early postoperative pressure sore formation.

NCT ID: NCT05534724 Recruiting - Orthopedic Disorder Clinical Trials

A Study to Compare Early and Partial Weight-bearing After Hallux Valgus Surgery

Start date: January 19, 2023
Phase: N/A
Study type: Interventional

This is a two-arm randomized controlled trial with the aim to evaluate the effectiveness and safety of post-operative management after a modified Lapidus arthrodesis with/without an Akin or a Weil/Hohmann surgery fusion with immediate complete weight-bearing compared with partial weight-bearing (10 - 15kg) for 6 weeks as a novel approach for rehabilitation after a foot surgery.

NCT ID: NCT05504538 Completed - Orthopedic Disorder Clinical Trials

Coracoid Tunnel Widening After ACJ Tight Rope Fixation

Start date: July 2016
Phase: N/A
Study type: Interventional

studying coracoid tunnel widening after arthroscopic fixation of acute acromioclavicular joint (ACJ) dislocation using TightRope system and its correlation with loss of reduction and the functional scores.

NCT ID: NCT05483673 Not yet recruiting - Orthopedic Disorder Clinical Trials

Analyzing Orthopedic Patient Experience Patterns in Medical Trials

Start date: August 2024
Phase:
Study type: Observational

Clinical study enrollment has historically been heavily biased toward specific demographics. Several people will be invited to participate in this study so that it may collect a variety of data about orthopedic clinical trial experiences and identify barriers to participation as well as the causes of participants' failure or withdrawal. People with orthopedic disorders who are invited to take part in medical research will benefit from the analysis of the data.

NCT ID: NCT05476198 Completed - Anxiety Clinical Trials

Brachial Plexus Block vs. General Anesthesia for Anesthesia Anxiety Before Orthopedic Upper Extremity Surgery

Start date: February 5, 2020
Phase: N/A
Study type: Interventional

Surgical procedures and anesthesia applications are situations in which people do not feel safe due to the current vital risks. Anxiety is a natural reaction that occurs in such situations, it manifests itself with worry and fear. Increased anxiety before surgery is associated with pathophysiological responses such as hypertension and dysrhythmia. Intense preoperative anxiety can increase morbidity, the need for anesthetic medication, and postoperative analgesia. For this reason, many questionnaire studies have been conducted to measure the degree of preoperative anxiety and to reveal its causes. The Amsterdam Preoperative Anxiety and Information Scale (APAIS) test has two parts that measure anxiety and the need for information about anesthesia and surgery. The APAIS-A (anxiety) part is the test that measures strain and shows whether the patient has anxiety about anesthesia or surgery. The APAIS-I (information) part estimates whether the person needs information. In the literature, the effects of general and spinal anesthesia techniques on preoperative anxiety levels have been compared for some specific surgical methods such as c-sections and perianal region surgeries. However, no study has been reported between peripheral nerve block and general anesthesia techniques. This study aimed to determine the effects of regional and general anesthesia methods on preoperative anxiety levels and the factors affecting these scores in patients who will undergo upper extremity surgery.

NCT ID: NCT05473611 Recruiting - Orthopedic Disorder Clinical Trials

Open Reduction Internal Versus Percutaneous Sacroiliac Screw Fixation in Unstable Posterior Ring Injury of Pelvic

Start date: March 10, 2022
Phase:
Study type: Observational

Surgical trearment of unstable posterior pelvic injuries can be performed with open reduction and internal fixation, closed reduction with percutaneous sacroiliac fixation. Biomechanically, no significant difference was found between the two methods in the literature. The aim of our study is to compare the radiological and clinical functional results of these methods.

NCT ID: NCT05461326 Recruiting - Clinical trials for Anterior Cruciate Ligament Injuries

Quadriceps Tendon Versus Bone Patellar Tendon Bone Autograft ACL Reconstruction RCT

Start date: September 26, 2023
Phase: N/A
Study type: Interventional

The choice of autograft for ACL reconstruction continues to be debated. To date, there has only be one completed randomized controlled trial with quad tendon to BTB and the tendon included a bone plug. There has been no study to date comparing an all soft tissue quad tendon to patellar tendon in a randomized controlled trial for ACL reconstruction.

NCT ID: NCT05447507 Completed - Orthopedic Disorder Clinical Trials

Comparison of Remimazolam and Dexmedetomidine for Intraoperative Sedation

Start date: July 8, 2022
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the sedation efficacy of dexmedetomidine and remimazolam for intraoperative sedation during regional block.

NCT ID: NCT05432505 Not yet recruiting - Orthopedic Disorder Clinical Trials

Ligamentum Teres Tenodesis in Developmental Dysplasia of the Hip

Start date: July 21, 2022
Phase:
Study type: Observational

The treatment of developmental dysplasia of the hip (DDH) remains challenging, yet recent advances have refined our understanding of how best to survey for the condition during infancy, minimize complications during early treatment, and refine the selection of patients who can best benefit from hip preservation surgery. The ideal continued target would be to prevent missed hip dislocations or dysplasia during the infant period, prevent avascular necrosis (AVN) during early treatment, and decrease the incidence of total hip arthroplasty in adulthood related to undertreated DDH, The goal of the treatment is to achieve a concentric reduction of the femoral head into the acetabulum.

NCT ID: NCT05427916 Terminated - Diabetes Clinical Trials

Closed Incision Negative Pressure Wound Therapy vs. Foam as Post Operative Dressing

Start date: July 12, 2022
Phase: N/A
Study type: Interventional

The primary objective is to assess the frequency of a wound healing complication, in a closed incisional wound in a "high risk" surgical incision when treated with Negative Pressure Wound Therapy versus a highly absorbent antimicrobial post - operative absorbent dressing.