KCT0007636Not yet recruiting未知
Prognostic impact of preoperative echocardiography in elderly patients with fragility hip Fracture: A Randomized Controlled Trial
The Catholic University of Korea, Eunpyeong St. Mary's Hospital0 sites160 target enrollmentStarted: TBDLast updated:
Conditions
Trial Snapshot
- Phase
- 未知
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 160
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional Study
Eligibility Criteria
- Ages
- 65(Year) to 100(Year) (—)
- Sex
- All
Inclusion Criteria
- •(1) For adults over the age of 65 who undergo surgical treatment for fragility hip fractures.
- •(2) ASA grade 3 or higher (1-3)
- •(3) Koval activity grade 5 or higher (1-5)
- •(4) Patients who are able to comply with and cooperate with outpatient follow-up, functional and radiological evaluation after surgery
- •(5) A patient who understands the study and has given written consent by the patient's own or the patient's representative to participate in the study.
Exclusion Criteria
- •(1) Patients who have difficulty breathing, chest pain, fainting or significant dizziness or who have worsened within the last 3 months
- •(2) ASA grade 4 and below (4-6)
- •(3) Patients with a revised cardiac risk index of 3 or higher
- •(4) Patients who were unable to walk independently prior to the fracture: Koval activity grade 6 or less (6-7)
- •(5) Among ASA grade 3 patients, if you have cardiovascular disease (heart failure, heart valve disease, coronary artery disease, coronary artery interventional strength, artificial pacemaker/intra-heart device retention, dialysis patients, serious arrhythmias such as atrial fibrillation, chronic obstructive pulmonary disease, etc.) and the evaluation of heart function has not been carried out within the last 1 year.
- •(6) If there was a previous local infection, sepsis, lower extremity vein thrombosis, etc. in the lower extremities at the surgical site
- •(7) Patients with past surgical history in the hip joint
- •(8) Patients who are not able to be tracked after alcohol and on an outpatient basis
Investigators
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