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Ankle Fractures clinical trials

View clinical trials related to Ankle Fractures.

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NCT ID: NCT05209347 Withdrawn - Ankle Fractures Clinical Trials

Custom Dynamic Orthoses to Reduce Articular Contact Stress

PRMRP FPA CT
Start date: December 2024
Phase: N/A
Study type: Interventional

The proposed study evaluates the effect of carbon fiber brace design on forces across the ankle. Research suggests that ankle arthritis develops following ankle fracture due, in part, to elevated forces on the cartilage. It is expected that carbon fiber braces can reduce forces in the ankle joint thereby reducing the risk of developing arthritis following injury. In this study, carbon fiber braces will be tested to determine how they influence the forces acting on the ankle cartilage. The proposed study will provide evidence that can be used by clinicians and researchers to design carbon fiber braces to effectively reduce forces on ankle cartilage.

NCT ID: NCT04768478 Withdrawn - Ankle Fractures Clinical Trials

CBD for Pain Reduction and Opioid Use After Ankle and Tibia Fracture ORIF

Start date: October 1, 2021
Phase: Phase 4
Study type: Interventional

The purpose of this study is to evaluate the effects of administering CBD to control post-operative pain in patients undergoing ankle fracture open reduction and internal fixation, tibial plafond (pilon) open reduction and internal fixation, tibial shaft repair (open reduction internal fixation or intramedullary nail fixation), or tibial plateau open reduction and internal fixation. Secondly, the purpose is to evaluate the effectiveness of CBD in comparison with opioid therapy for post-operative pain.

NCT ID: NCT04303663 Withdrawn - Ankle Fractures Clinical Trials

Fibular Nail vs Plate in Ankle Fractures

Start date: January 1, 2022
Phase: N/A
Study type: Interventional

Randomised Controlled Trial to Compare the Efficacy of Fibular Nail Fixation vs Plate Fixation in Ankle Fracture Management

NCT ID: NCT04086927 Withdrawn - Ankle Fractures Clinical Trials

Unna Boots for Ankle Fracture Swelling

Start date: January 31, 2021
Phase: N/A
Study type: Interventional

This study will evaluate the difference in soft tissue swelling prior to surgery and wound complications after surgery between unna boot application versus standard splint application. An unna boot is an extra zinc covered wrap around your leg followed by standard splint application (cotton dressing, plaster, then soft dressing). Prior to surgery the participant's swelling will be measured and compared to the standard splint application group. After surgery, the participant will be monitored for wound complications, pain, and range of motion.

NCT ID: NCT03084263 Withdrawn - Ankle Fractures Clinical Trials

Arthroscopic Assisted Open Reduction Internal Fixation Versus Open Reduction Internal Fixation in Ankle Fractures

Start date: May 1, 2017
Phase: N/A
Study type: Interventional

The objective of this study is to compare the functional outcomes of patients with ankle fractures treated by Arthroscopic assisted Open Reduction Internal Fixation (AORIF) versus Open Reduction Internal Fixation (ORIF).

NCT ID: NCT02863042 Withdrawn - Ankle Fracture Clinical Trials

Is Deltoid Ligament Repair for Ankle Fracture Necessary?

AnkleFX
Start date: May 2016
Phase: N/A
Study type: Interventional

The investigator hypothesizes that primary acute ankle deltoid ligament repair can help restore ankle radiographic congruity and functional outcomes.

NCT ID: NCT02281968 Withdrawn - Clinical trials for Closed Fracture of Ankle

NSAIDs for Pain After Ankle Fracture Surgery

Start date: December 2014
Phase: Phase 4
Study type: Interventional

The purpose of this study is to investigate if it is possible to decrease opioid consumption in patients undergoing ankle fracture surgery by providing scheduled doses of nonsteroidal inflammatory drugs (NSAIDs). This is a prospective, randomized, double-blinded, placebo controlled study with two groups of patients: one getting NSAIDs to take at regularly scheduled times plus a traditional prescription for opioid medication and one receiving the traditional prescription for opioid medication and a placebo. Patients will be assigned to a group from a computer-generated program. Neither the patients nor their doctors or nurses will know what group they are in, only the pharmacist will have that information. Patients in both groups will have the opportunity to take opioid medications if the pain becomes unmanageable.

NCT ID: NCT01923623 Withdrawn - Clinical trials for Ankle Fracture in Need of Surgical Fixation

The Effect of Nerve Blockades in Addition to General Anesthesia in Surgical Fixation of Ankle Fractures.

Start date: July 1, 2013
Phase: Phase 4
Study type: Interventional

This clinical, randomized, and controlled study will provide valuable scientific evidence regarding the effect of adding peripheral nerve blockades to general anaesthesia during ankle surgery. In particular, the investigators want to determine if the need for postoperative opioids will be reduced and whether this will lead to shorter admission to recovery room and fewer instances of side effects such as postoperative nausea and vomiting. In addition, the investigators will determine whether the functional outcome is improved i.e. faster and more successful rehabilitation. This would have profound benefits not only to the individual patient but also to society by reducing expenses during admission, the cost of sick leave etc.