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Hip Fractures clinical trials

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NCT ID: NCT06443892 Recruiting - Pain, Postoperative Clinical Trials

Comparison of Pain Relief After Hip Fracture Surgery: Hip and Groin Nerve Block

Start date: May 1, 2023
Phase:
Study type: Observational

This observational prospective double-blind study aims to compare the analgesic effectiveness of the pericapsular nerve group block (PENG) group and the suprainguinal fascia iliaca compartment block(SFICB) group to be applied to relieve postoperative pain in participants over the age of 18 who will be treated under spinal anesthesia with intertrochanteric femur fracture. The main question it aims to answer is: * Demonstration of whether PENG block or SFICB is more effective for postoperative analgesia in patients who have undergone intertrochanteric femur fracture surgery, based on pain scores, opioid consumption and patient satisfaction. ıntertrochanteric femur fractures cause severe pain with movement. Postoperatively, participants' movements are severely restricted, increasing the likelihood of complications. In this study, participants' pain status, VAS score, opioid consumption through patient-controlled analgesia, and satisfaction will be measured with a survey at the end of the 24th hour.

NCT ID: NCT06425627 Recruiting - Anesthesia Clinical Trials

Spinal Versus General Anesthesia on Postoperative Pulmonary Complications

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

The objective of this study was to investigate the difference in postoperative pulmonary complications (PPCs) between spinal anesthesia and general anesthesia in patients undergoing delayed hip surgery.

NCT ID: NCT06389279 Recruiting - Hip Fracture Clinical Trials

The Effect of Facial Plane Blocks on Postoperative Recovery Quality in Hip Surgery

Start date: April 30, 2024
Phase:
Study type: Observational

The aim of this study was to evaluate the effect of ultrasound-guided pericapsular nerve block, fascia iliaca compartment block, and femoral block on the quality of recovery as part of multimodal analgesia before hip surgery under spinal anesthesia.

NCT ID: NCT06380439 Recruiting - Pain, Postoperative Clinical Trials

The Effect of Wrist Ankle Acupuncture on Post-Total Hip Arthroplasty Pain

Start date: April 23, 2024
Phase: N/A
Study type: Interventional

Total hip arthroplasty is one of the most cost-effective orthopedic surgical procedures which can restore hip function and improve the patient's quality of life. However, total hip arthroplasty is significantly associated with postoperative pain. Pain after total hip arthroplasty surgery can adversely affect the patient's early postoperative recovery, postoperative mobility, and hinder rehabilitation. Wrist ankle acupuncture (WAA) is a simpler acupuncture technique, using fewer points, shallow needle insertion and lighter stimulation. Wrist-ankle acupuncture as multimodal analgesia after orthopedic surgery is useful for reducing pain and reduce the incidence of post-surgical side effects. The primary aim of this study is to investigate whether wrist ankle acupuncture therapy gives better and results for post total hip arthroplasty pain than sham wrist ankle acupuncture

NCT ID: NCT06357312 Recruiting - Hip Fracture Clinical Trials

Influence of Static Distal Locking of a Short Proximal Femoral Nail

Start date: April 1, 2024
Phase: N/A
Study type: Interventional

Prospective, comparative, randomized, double-blind study to evaluate the outcomes of trochanteric nailing in unstable hip fractures with and without a distal interlocking screw.

NCT ID: NCT06342479 Recruiting - Surgical Wound Clinical Trials

Discharge Training for Patients With Intertrochanteric Fracture

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

This study examines the effect of discharge training given to patients with intertrochanteric femur fractures on the wound healing process and readiness for discharge. In the study, patients were provided with certain educational content before and after discharge. The effect of training on wound healing, readiness for discharge and post-discharge recovery process will be evaluated statistically.

NCT ID: NCT06329271 Recruiting - Clinical trials for Bony Weight Bearing Disorder

After Hip Fracture Nailing, Compare Early Weight Bearing as Tolerated (WBAT) Group With Weight Bearing Restriction(WBR)

Start date: March 8, 2024
Phase: N/A
Study type: Interventional

Purpose: Proximal femur fracture is a major traumatic injury in elderly populations; however, practical postoperative weight-bearing protocols are lacking. Therefore, the purpose of the present study was to investigate whether early weight-bearing status after proximal femur nail fixation is associated with any loss of reduction and evaluate the clinical outcomes of this intervention. Patients and methods: For this prospective single-center clinical trial study, we recruited 60 geriatric proximal femur fracture cases, classified by AO/OTA 2018, receiving intramedullary nail fixation. The participants were assigned to the Early-weight-bearing group (n= 30) or the Weight-bearing restriction group (n = 30). Clinical outcomes included the Harris functional hip score and VAS pain score. Additionally, demographic data, radiological parameters, time to weight-bearing, mortality rate, medical and surgical complications, and final ambulation status were recorded.

NCT ID: NCT06311630 Recruiting - Hip Fracture Clinical Trials

Comparative Study of Analgesic Effect of Ultrasound Guided PENG Block vs FEMORAL BLOCK in Hip Fracture

Start date: May 20, 2023
Phase:
Study type: Observational

To study the analgesic effect of ultrasound guided PENG Block vs Femoral nerve block in patients with Hip fracture presenting to Emergency department

NCT ID: NCT06304584 Recruiting - Hip Fractures Clinical Trials

Cross-sectoral Rehabilitation of Older High-risk Patients With Hip Fracture

Start date: May 15, 2023
Phase:
Study type: Observational

The goal of this observational study is to learn about and monitor the cross-sectoral rehabilitation process in older high-risk patients treated for at fragility fracture of the hip. The main questions aim to answer: - how patients are doing up to one year after hip fracture surgery on different outcomes across the continuum of rehabilitation being offered - what expectations, experiences and satisfaction patients have for the overall rehabilitation process after a hip fracture Participants age 65 and above with home address in Frederiksberg municipality, living in own home, admitted and treated for at hip fracture at Department of Orthopedic Surgery, Bispebjerg Hospital, will be asked for participation.

NCT ID: NCT06294665 Recruiting - Hip Fractures Clinical Trials

Comparison Between Bupivacaine-Dexmedetomidine Versus Bupivacaine-Dexamethasone in Pericapsular Nerve Group (PENG) Block

Start date: March 1, 2024
Phase: Phase 1
Study type: Interventional

The aim of this work is to compare the effectiveness of bupivacaine- dexmedetomidine mixture versus bupivacaine-dexamethasone mixture in PENG Block as Post-operative Analgesia in Hip surgeries