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临床试验/NCT07720856
NCT07720856招募中不适用

Surgical Recovery Support Pillow for Spine Surgeries

Montefiore Medical Center1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2026年8月10日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
10
试验地点
1
主要终点
Pillow use

研究概览

简要总结

The present study investigates the feasibility of a support pillow for use after spinal surgical procedures, and more particularly, to protect the midline region of the back following spinal surgery.

Existing cushioning pillows do not accommodate the anatomy of the human back nor the requirements of isolating a vertical spinal incision. For example, donut-style or ring-shaped pillows are designed for entirely different purposes, such as hemorrhoidal relief, and cannot provide the desired spinal relief. As a result, there is no suitable, dedicated support structure that allows a patient to rest on their back while eliminating pressure on the surgical site. Accordingly, there is a need for a device that permits postoperative spinal surgery patients to sit or lie in a supine or reclined position without the surgical incision contacting or being compressed by any supporting surface.

详细描述

The investigators hypothesize that use of the back saver pillow as currently designed will be feasible and that patients will report subjective improvement in pain when applying the pillow. Our specific aims are two-fold, namely (1) Determine if patients are able to utilize the back saver pillow as currently designed and (2) Survey patients as to whether they feel the back saver pillow was beneficial for their recovery.

Our study design is as follows. Eligible patients will be asked pre-op whether they would like to be part of this study and asked for informed consent prior to surgery. A total of 10 patients will be recruited. Enrolled patients will be provided with the back saver pillow either while admitted, if inpatient, or at the time of discharge for same-day surgery patients. Patients will be asked to fill out a survey with questions related to how easy the pillow was to use and whether they found it to reduce their pain on the rating scale of 1-10, where 1 is no pain and 10 is most painful. There will be 3 survey timepoints post-surgery: (1) on the day following surgery, (2) right before discharge and (3) 2-weeks post-surgery. Surveys will assess patient feedback about ease of use, and pain, first without the pillow in the supine position and sitting up with the back against another surface, then with the pillow in the supine position and sitting up with the back against another surface.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Supportive Care
盲法
None

入排标准

年龄范围
19 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Adult patients who have lumbar fusion surgery, who consent to participate

排除标准

  • •Pediatric patients 18 years old and under

研究组 & 干预措施

Participant

Experimental

Surgical Recovery Support Pillow

干预措施: Surgical Recovery Support Pillow (Device)

结局指标

主要结局

Pillow use

时间窗: One day after surgery, on discharge day (approximately 1-3 days after surgery) and 2 weeks after surgery

Pillow use will be measured as a dichotomous measure of whether or not the pillow was used. Results will be summarized.

次要结局

  • Pillow comfort and pain(One day after surgery, at discharge (approximately 1- 3 days after surgery) and 2 weeks after surgery)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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