Assessment of therapeutic clinical trials for proximal humeral fractures

被引:0
作者
Koa, Jonathan [1 ]
Fares, Mohamad Y. [1 ]
Daher, Mohammad [1 ]
Abboud, Joseph A. [1 ]
机构
[1] Rothman Orthopaed Inst, Div Shoulder & Elbow Surg, 925 Chestnut St, Philadelphia, PA 19107 USA
来源
CLINICS IN SHOULDER AND ELBOW | 2024年 / 27卷 / 02期
关键词
Proximal humerus fracture; Shoulder; Treatment; Trial; Systematic review; REVERSE SHOULDER ARTHROPLASTY; SURGICAL-TREATMENT; ELDERLY-PATIENTS; PLATE FIXATION; HEMIARTHROPLASTY; EPIDEMIOLOGY; SUPERIOR; SURGERY; RISK;
D O I
10.5397/cise.2023.00521
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Proximal humeral fractures (PHFs) are a common injury among the older population. An ideal therapeutic protocol has yet to be developed, and numerous clinical trials are being conducted to find the best therapeutic approach. The purpose of this study is to evaluate the current body of knowledge available via interventional clinical trials. In December 2022, interventional clinical trials relating to PHFs on Clinicaltrials.gov were screened. Trial characteristics included duration, status, intervention, phase, outcomes, location, and study design. Publications associated with each trial were searched on PubMed/Medline using the ClinicalTrials.gov registry number. The final dataset comprised 64 trials. The most common trial status was completed (36%). The majority did not have a Food and Drug Administration-defined phase (67%), was randomized (81%), involved a single facility (72%), used a parallel assignment intervention model (80%), and used an open-label approach (45%). Eleven trials were associated with a publication, and the publication rate was 17%. Average enrollment was 86 participants, and mean trial duration was 51.4 months. Europe/UK/Russia/Turkey participated in the most trials (70%). Most of the trials were initiated after 2010 (87.5%). Procedure-related interventions (55%) were most common. Disability/function was the most common primary outcome assessed (61%). The low publication rate and the multitude of trials conducted after 2010 highlight the urgency and need for trial results to be published to establish an ideal therapeutic protocol. Since the majority of the trials involved a single institution and an open-label approach, reinforcing blinding and establishing multi-centered trials can improve the validity of the clinical trial results.
引用
收藏
页码:237 / 246
页数:10
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