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Hip Dislocation, Congenital clinical trials

View clinical trials related to Hip Dislocation, Congenital.

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NCT ID: NCT06442722 Not yet recruiting - Clinical trials for Developmental Dysplasia of the Hip

Surgical Treatment of DDH With and Without Capsulorrhaphy

Start date: June 2, 2024
Phase: N/A
Study type: Interventional

The goal of this interventional study is to evaluates the surgical treatment outcomes of Developmental Dysplasia of Hip with and without capsulorrhaphy between 1-6 years of age . it compares the effectiveness of these approaches in improving postoperative stability , range of motion , and long-term success rates for DDH patients undergoing surgery .:

NCT ID: NCT06439147 Enrolling by invitation - Clinical trials for Developmental Dysplasia of the Hip

Comparison Between Two Techniques of Capsulotomy During Capsulorrhaphy in Cases of Developmental Dysplasia of the Hip

Start date: October 11, 2023
Phase: N/A
Study type: Interventional

comparison of the outcome between using U-shaped incision and T-shaped incision for capsulorrhaphy in management of Developmental dysplasia of the hip

NCT ID: NCT06408987 Not yet recruiting - Clinical trials for Developmental Dysplasia of the Hip

Arthroscopically Assisted Versus Open Surgical Reduction of the Hip in Patients With Irreducible DDH Before the Walking Age

Start date: May 15, 2024
Phase: N/A
Study type: Interventional

To determine the role of arthroscopy in treatment of the DDH.

NCT ID: NCT06233487 Not yet recruiting - Clinical trials for Developmental Dysplasia of the Hip

Reliability of Ultrasound Metrics Used in Hip Dysplasia Diagnostics - a Prospective Study

Start date: February 20, 2024
Phase: N/A
Study type: Interventional

Several measurements are used to evaluate hip dysplasia in hip ultrasound of children. Despite having being used since the 1980s, reliability studies have failed to find acceptable reliaiblity values for the gold standard ultrasound methods. This study will evaluate three ultrasound measurement methodologies in a high quality controlled setting, to investigate the best achieveable reliability and agreement of the investigated measurements used in hip dysplasia diagnostics.

NCT ID: NCT06209255 Completed - Hip Osteoarthritis Clinical Trials

Pelvic Osteotomy Of The Total Hip Replacement

Start date: August 11, 2020
Phase:
Study type: Observational

This observational study aims to learn about the outcomes in the previously operated patient and whether pelvic bone rearrangement surgery was a success. The main question it aims to answer is: • Should the investigators perform pelvic rearrangement surgery on a patient if there's not enough bone stock to accomplish the exchange of the components? As the research started the participant was asked to attend outpatient clinics regularly and keep in touch. The investigators were able to observe the outcomes and closely explore probable risks for failure.

NCT ID: NCT06189781 Recruiting - Pain, Postoperative Clinical Trials

Pain Injection Versus Epidural Anesthesia for Hip Surgery in Pediatric Patients With Cerebral Palsy

Start date: December 1, 2023
Phase: Phase 4
Study type: Interventional

Pain management in pediatric patients presents a difficult challenge. Unlike adults, pediatric patients often cannot communicate their pain management needs clearly. This is especially true in patients with cerebral palsy (CP), who often have concomitant developmental delay, intellectual disability and verbal limitations. Current literature indicates pain as a common experience for children with CP but has been understudied in this population. Moreover, inadequate post-operative pain control can result in negative physiologic and psychological complications and lead to poor surgical outcomes. Currently, perioperative pain management following orthopaedic procedures in pediatric patients follows traditional protocols that rely on the administration of opioid medications despite their known adverse side effects including nausea, vomiting, itching, constipation, urinary retention, confusion, and respiratory depression. Epidural anesthesia is a key modality in traditional pain management for pediatric patients with CP given its proven efficacy in decreasing pain and managing spasticity. Yet, administering epidural anesthesia in this patient population poses several risks including damage to preexisting intrathecal baclofen pumps, iatrogenic infection, and technically demanding insertion given high rates of concomitant neuromuscular scoliosis. Alternatively, multimodal analgesic injections theoretically offer an efficacious adjunct to traditional pain management protocols with a lower risk profile. Preliminary data from our study group's pilot randomized control trial comparing the safety and efficacy of a multimodal surgical site injection to placebo showed decreased pain scores and narcotic consumption postoperatively in this patient population. Based on these promising results, the objective of this randomized control trial is to evaluate the efficacy of a multimodal surgical site injection compared to epidural anesthesia for postoperative pain control following operative management of hip dysplasia in pediatric patients with CP.

NCT ID: NCT06176612 Active, not recruiting - Clinical trials for Total Hip Arthroplasty

In Patients With Hip Dysplasia, Mid-Term Lower Extremities and Spine After Hip Arthroplasty Natural Course

Start date: April 15, 2021
Phase: N/A
Study type: Interventional

Patients with developmental hip dysplasia often present to the outpatient clinic in adulthood with hip pain due to progressive hip osteoarthritis. However, they may have complaints such as limping, lumbar lordosis, lower back pain, and leg length difference. Today, the best treatment option for these patients is hip arthroplasty. Hip arthroplasty causes a high rate of functional improvement and pain relief. According to the hip arthroplasty technique applied, improvement in lameness, leg length difference and spinal curvatures is expected. The aim of our study is to show the change in postoperative spine and lower extremity curvatures after hip arthroplasty in patients with advanced developmental hip dislocation.

NCT ID: NCT06130761 Recruiting - Hip Dysplasia Clinical Trials

Pericapsular Block Versus Trans Muscular Quadratus Lumborum Block in Patients Undergoing Correction of Hip Dysplasia

Start date: January 1, 2023
Phase: N/A
Study type: Interventional

The aim of our study to compare the analgesic effect of pericapsular nerve group block combined with lateral femoral cutaneous nerve block and trans muscular quadratus Lumborum Block block perioperatively in pediatric patients undergoing developmental dysplasia of the hip surgical repair

NCT ID: NCT06087549 Completed - Hip Fractures Clinical Trials

PENG Block vs. ESP Block for Pediatric Hip Surgery

Start date: October 17, 2023
Phase: Phase 4
Study type: Interventional

The study compares the effectiveness and safety of the pericapsular nerve blockade vs. ESPB in pediatric patients who underwent hip surgeries.

NCT ID: NCT06037278 Recruiting - Clinical trials for Acetabular Dysplasia

Patient Specific Guides and Surgical Planning for Periacetabular Osteotomy; Post Marketing Evaluation Study

MyPAO
Start date: July 13, 2023
Phase: N/A
Study type: Interventional

A case series to provide post marketing evaluation of the MyPAO surgical planning and patient specific guides technology. This will be a single-centre, multi-surgeon evaluation assessing the safety of the use of these guides in periacetabular osteotomy surgery.