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Fractures, Bone clinical trials

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NCT ID: NCT03753100 Completed - Clinical trials for Femoral Neck Fractures

Periprosthetic Bone Remodeling in Femoral Neck Fracture Patients; a 5-year Follow up Study

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

Periprosthetic bone remodeling in femoral neck fracture patients: a 5-year follow up study addressing the influence of surgical approach on periprosthetic bone mineral density.

NCT ID: NCT03749616 Completed - Clinical trials for Distal Radius Fracture

Effect of NSAID Use on Pain and Opioid Consumption Following Distal Radius Fracture

Adult NSAID
Start date: January 2, 2019
Phase: Phase 4
Study type: Interventional

Non-steroidal anti-inflammatory drugs (NSAIDs), such as ibuprofen, are excellent medications for providing pain control in certain patients. There is some data to suggest that NSAIDs can be used to reduce postoperative pain and narcotic use in patients who had undergone carpal tunnel release. There are mixed results about the effect of bone healing in adult patients with broken bones. The investigators hypothesize that NSAID administration in the acute phase of distal radius fracture healing will be non-inferior for pain control and decrease the use of opioid analgesics compared to patients who take acetaminophen for pain control during this same time period. Furthermore, the investigators hypothesize that patients will have similar or better patient reported outcomes, range of motion, and strength with the administration of NSAIDs.

NCT ID: NCT03749174 Completed - Radial Fracture Clinical Trials

Radius Fracture Anesthesia and Rehabilitation (RADAR)

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

Distal fracture of the radial bone is the commonest fracture and is also connected to osteoporosis. Normally the operation is performed under neuroaxial blockade and sedation. When the blockade rapidly vanish many patients experience a rebound pain much severer that than the actual trauma pain. If long acting local anesthetics are used this will occur during night time and many patients will go to the emergency room for pain treatment. Short acting local anesthetics may make it possible to treat patients pain in-house prior to leaving the hospital. In this study

NCT ID: NCT03749122 Completed - Surgery Clinical Trials

Time to Hip Fracture Surgery

Start date: January 1, 2006
Phase:
Study type: Observational

The purpose of the study is to evaluate how time from hospital admission to start of surgery influence mortality in patients with acute hip fracture. Data on patients with hip fracture surgery will be collected from the hospital's registration system and will be analyzed regarding age, gender, American Society of Anesthesiologists (ASA) Physical Status Classification, type of surgery and time from admission to surgery along with data on mortality.

NCT ID: NCT03747666 Not yet recruiting - Mandible Fracture Clinical Trials

Single Locking Miniplate and Two Non-locking Miniplates in the Management of Parasymphyseal Fracture

Start date: November 2019
Phase: N/A
Study type: Interventional

Evaluating the biting force after management of parasymphyseal fracture in patients with two-line mandibular fractures.

NCT ID: NCT03741556 Completed - Ankle Fractures Clinical Trials

Prognostic Factors Following Ankle Fractures

Start date: November 7, 2018
Phase:
Study type: Observational [Patient Registry]

Ankel fractures is a common fracture. Most patients experience that the regain normal range of motions and limited pain within the first 6 months following ankel fracture, but not all. The aim of the study is to determine if any prognostic factors is associated with a worse outcome.

NCT ID: NCT03730207 Completed - Clinical trials for Pathological Fracture of Vertebra Due to Secondary Osteoporosis (Disorder)

Xpede Clinical Study

Start date: December 18, 2018
Phase: N/A
Study type: Interventional

The purpose of this clinical study is to confirm the efficacy and safety of the Kyphon®Xpede™ Bone Cement in human use in China.

NCT ID: NCT03724773 Withdrawn - Clinical trials for Closed Fracture of Shaft of Ulna

Long-Arm vs Sugar-Tong

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

The purpose of this study is to determine whether a sugar-tong splint is as effective as a long-arm cast in maintaining reduction of pediatric forearm shaft fractures in a randomized, prospective manner. Consented participants will be randomly assigned to be treated with either a sugar-tong splint or a long-arm cast (both standard of care treatments) in REDCap. Each participant will have a 50/50 chance of being assign to either treatment.

NCT ID: NCT03724422 Terminated - Radiation Therapy Clinical Trials

HO Prophylaxis Therapy for Distal Humerus Fractures

Start date: October 9, 2019
Phase: N/A
Study type: Interventional

To determine the effectiveness of 500 cGy dose of radiation therapy vs. an untreated group in the prophylactic treatment of heterotopic ossification in distal humerus fractures

NCT ID: NCT03721835 Terminated - Clinical trials for Femoral Neck Fractures

Safety Study of Femoral Neck Fracture System

CONQUEST FN
Start date: September 10, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the reoperation rate of fractures that have occurred at the neck of the femur that are treated with the CONQUEST FN Femoral Neck Fracture System. The CONQUEST FN Femoral Neck Fracture System is approved for use by the United States Food and Drug Administration (FDA). It consists of a stainless steel plate and up to three (3) screws intended to treat both non-displaced and displaced fractures to the femoral neck.