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Hip Surgery clinical trials

View clinical trials related to Hip Surgery.

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NCT ID: NCT05802589 Completed - Pain, Postoperative Clinical Trials

Comparison of the Efficiency of PENG Block and ESP Block Used for Postoperative Analgesia in Elective Hip Surgery

Start date: May 17, 2021
Phase: N/A
Study type: Interventional

The aim of the study is to determine whether the traditional intravenous analgesia technique or the ultrasound-guided pericapsular nerve group block or the unilateral erector spina plane block technique is superior in postoperative analgesia management in the hip operation procedure that requires preoperative and postoperative severe analgesia. In this way, by preventing the health problems that may occur due to the pain of the patients after the operation; to provide benefits for the early mobilization of patients, shortening the hospital stay, reducing the cost and increasing patient satisfaction.

NCT ID: NCT03954730 Completed - Hip Surgery Clinical Trials

Eccentric Training Versus Active Release Technique On Quadriceps In Patients With Dynamic Hip Screw

Start date: March 19, 2019
Phase: N/A
Study type: Interventional

This study will compare the effects of Eccentric training and Strength training with priory applied Active Release Technique on Quadriceps muscle in post operative patients of Dynamic Hip screw. Participants would be equally divided into two groups each receiving specific type of protocol besides standard post operative protocol of Dynamic Hip screw

NCT ID: NCT03190447 Completed - Nursing Clinical Trials

Wich is the Best Dressing in Wounds by Primary Surgery of THA and / or TKA?

Start date: April 20, 2017
Phase: N/A
Study type: Interventional

Surgical wounds are covered to prevent bleeding, absorb the exudates and provide a barrier against external contamination. Currently, in Corporació PT after orthopedic surgery, traditional occlusive dressing of sterile gauze and non-woven hypoallergenic adhesive tape is placed. In many cases the appearance of blistering caused by the use of these conventional dressings is observed, which increases the risk of infection, pain and the final cost of the procedure. There are other types of dressings that could improve these aspects but comparative data are not currently available. Main objective: to identify the dressing that better preserves the integrity of the skin. Design: Prospective randomized comparative study of 5 types of dressings used in total knee and hip arthroplasty surgical wounds (TKA and THA). Secondary Objectives: To identify the dressing that provides greater advantages and minor inconveniences in TKA and THA surgery. Study population: Patients older than 18 years undergoing fast track primary TKA or THA. 110 patients

NCT ID: NCT01988818 Completed - Knee-surgery Clinical Trials

Prospective, Randomized Study of 2 Different Wound Dressings

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Start date: April 2014
Phase: N/A
Study type: Interventional

The primary objective of this investigation is to evaluate the performance of a self-adhesive absorbent post-operative dressing coated with a soft silicone layer in minimize the risk of the development of blistering in subjects after hip or knee arthroplasty or spinal surgery in comparison to a standard wound dressing The secondary objectives are to evaluate: - the performance of the dressing - the comfort, conformability and the acceptability of the dressing - pain before, during and after dressing removal - the overall cost regarding dressing wear time, time to do dressing change and personal resources needed

NCT ID: NCT01875289 Completed - Hip Surgery Clinical Trials

Efficacy of a Modified Obturator Nerve Block Technique

Start date: July 2013
Phase: N/A
Study type: Interventional

Efficacy of a modified obturator nerve block technique by using only a single morphological landmark, a double-blinded randomised pilot study.

NCT ID: NCT01469871 Completed - Hip Surgery Clinical Trials

Evaluation of Three Types of Dressings After Hip Surgery

Start date: February 2009
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if one of the new types of dressings (MEPORE PRO and/or MEPILEX BORDER ) will reduce the blister rate compared to the currently used HYPAFIX.

NCT ID: NCT00890123 Completed - Hip Surgery Clinical Trials

Preoperative Intravenous Omega 3 Fatty Acids Administration in Elderly Patients Undergoing Hip Surgery

Start date: April 2009
Phase: Phase 4
Study type: Interventional

The perioperative administration of n-3 fatty acids has been shown to lead to favorable effects on outcome in patients with severe surgical interventions by lowering the magnitude of inflammatory response and by modulating the immune response. No study with preoperative administration of IV omega 3 fatty acids as a part of total parenteral nutrition (TPN) or monotherapy with it to demonstrate its effects on inflammatory and immune response has been conducted. So, this study has been planned to judge the inflammatory response of preoperative monotherapy with IV omega 3 fatty acids in elderly patients undergoing hip surgery considering the hyper-inflammation associated with this type of surgery in elderly patients.