Evaluation of the efficacy and safety of conventional and interlaminar full-endoscopic decompressive laminectomy to treat lumbar spinal stenosis (ENDO-F trial): Protocol for a prospective, randomized, multicenter trial.
Jin-Sung L KimJunseok BaeDong Chan LeeSang-Ha ShinHan Joong KeumYoung Soo ChoiSang Soo EunSeung Ho ShinHyun Jin HongJi Yeon KimTae Hyun KimWoojung LimJunghoon KimSang-Min ParkHyun-Jin ParkHong-Jae LeePublished in: PloS one (2023)
Lumbar spinal stenosis is a common spinal degenerative condition. Minimally invasive interlaminar full-endoscopic decompressive laminectomy provides greater patient satisfaction and faster recovery than open decompressive laminectomy. The aim of our randomized controlled trial will be to compare the safety and efficacy of interlaminar full-endoscopic laminectomy and open decompressive laminectomy. Our trial will include 120 participants (60 per group) who will undergo surgical treatment for lumbar spinal stenosis. The primary outcome will be the Oswestry Disability Index measured at 12 months postoperatively. Secondary patient-reported outcomes will include back and radicular leg pain measured via a visual analog scale; the Oswestry Disability Index; the Euro-QOL-5 Dimensions score measured at 2 weeks and at 3, 6, and 12 months postoperatively; and patient satisfaction. The functional measures will include time to return to daily activities postoperatively and walking distance/time. The surgical outcomes will include postoperative drainage, operation time, duration of hospital stay, postoperative creatine kinase (an indicator of muscle injury) level, and postoperative surgical scarring. Magnetic resonance and computed tomography images and simple radiographs will be obtained for all patients. The safety outcomes will include surgery-related complications and adverse effects. All evaluations will be performed by a single assessor at each participating hospital who will be blinded to group allocation. The evaluations will be conducted preoperatively and at 2 weeks and 3, 6, and 12 months postoperatively. The randomized, multicenter design of the trial, blinding, and justification of the sample size will reduce the risk of bias in our trial. The results of the trial will provide data regarding the use of interlaminar full-endoscopic laminectomy as an alternative to open decompressive laminectomy that results in similar surgical findings with less invasiveness. Trial registration: This trial is registered at cris.nih.go.kr. (KCT0006198; protocol version 1; 27 May 2021).
Keyphrases
- phase iii
- study protocol
- minimally invasive
- randomized controlled trial
- phase ii
- clinical trial
- open label
- patient satisfaction
- computed tomography
- patient reported outcomes
- magnetic resonance
- ultrasound guided
- patients undergoing
- placebo controlled
- metabolic syndrome
- type diabetes
- magnetic resonance imaging
- emergency department
- machine learning
- spinal cord
- chronic pain
- acute coronary syndrome
- systematic review
- positron emission tomography
- neuropathic pain
- adipose tissue
- atrial fibrillation
- skeletal muscle
- contrast enhanced
- image quality