Curved versus Straight Stem Uncemented Total Hip Arthroplasty Osteoarthritis Multicenter trial (CUSTOM): design of a prospective blinded randomised controlled multicentre trial

被引:4
作者
van Beers, Loes W. A. H. [1 ]
van Oldenrijk, Jakob [2 ]
Scholtes, Vanessa A. B. [1 ]
Geerdink, Carel H. [3 ]
Niers, Bob B. A. M. [3 ]
Runne, Wouter [1 ]
Bhandari, Mohit [4 ]
Poolman, Rudolf W. [1 ]
机构
[1] OLVG, Joint Res, Dept Orthopaed Surg, Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Dept Orthopaed Surg, Meibergdreef 9, NL-1105 AZ Amsterdam, Netherlands
[3] Ikazia Hosp, Dept Orthopaed Surg, Rotterdam, Netherlands
[4] McMaster Univ Hosp, Dept Surg, Hamilton, ON, Canada
来源
BMJ OPEN | 2016年 / 6卷 / 03期
关键词
ORTHOPAEDIC & TRAUMA SURGERY; ORTHOPEDIC-SURGERY; PROSPECTIVE COHORT; LEARNING-CURVE; FOLLOW-UP; REPLACEMENT; SYSTEM; 10-YEAR; QUALITY; JOINT; DAMAGE;
D O I
10.1136/bmjopen-2015-010472
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Answering the demands of an increasingly young and active patient population, recent developments in total hip arthroplasty (THA) have shifted towards minimising tissue damage. The Collum Femoris Preserving (CFP) stem was developed to preserve the trochanteric region of the femur, which potentially preserves the insertion of the gluteus musculature. This might accelerate early postoperative rehabilitation and improve functional outcome. Currently the functional results of the CFP stem have not been compared with conventional straight stems in a randomised controlled trial (RCT). The primary purpose of this trial is to compare the functional result of CFP stem THA with conventional uncemented straight stem THA, measured by the Dutch Hip disability and Osteoarthritis Outcome Score (HOOS) at 3-month follow-up. Methods A prospective blinded multicentre RCT will be performed. We aim to recruit 150 patients. The patients will be randomly allocated to a THA with a straight or a curved stem. All patients, research assistants, clinical assessors and investigators will be blinded for the type of prosthesis for 5years. Clinical assessments and roentgenograms will be taken preoperative, at 6weeks after surgery, at 1, 2, 3, 4 and 5years after surgery. Patient reported outcome measures (PROMs) will be obtained at the same follow-up moments. In addition, the PROMs will also be sent to the patients at 3 and 6months after surgery. The HOOS at 3-month follow-up will be our primary outcome. Ethics and dissemination This trial will be performed in accordance with the Declaration of Helsinki. A local ethics committee has approved this trial. Written informed consent will be obtained from all participating patients. All serious adverse events will be reported to the ethics committee. Results Results will be submitted for publication to an orthopaedics related journal. Trial registration number NTR1560.
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页数:7
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