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临床试验/NCT06580951
NCT06580951尚未招募不适用

Regenerative Peripheral Nerve Interface for Prophylaxis Against Post-Breast Surgery Pain

George Kokosis1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2026年10月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
200
试验地点
1
主要终点
Incidence of neuroma-related PBSPS

研究概览

简要总结

Regenerative peripheral nerve interface (RPNI) was first developed in 2012 by Dr. Paul Cederna at the University of Michigan as a means for amputees to control their prothesis with their minds. In the decade that followed, it was found RPNI surgery not only provided amputees with neuroma (a growth made up nerve tissue) pain relief but could help prevent neuroma from developing as well.

This single center, randomized controlled, investigator-initiated study will look at whether the RPNI, a nerve burying procedure involving protecting sensory nerves with a small piece of the patient's pectoralis muscle, performed at the time of the standard mastectomy with immediate breast reconstruction surgery can prevent and/or reduce the risk for long-term nerve pain after breast cancer surgery (also called neuroma-related post-breast surgery pain syndrome (PBSPS)) versus the standard surgery alone (Control group). Symptoms of PBSPS include discomfort, numbness, tingling, and shooting pain in the chest and breast area. It is relatively common and may have many causes.

About 200 adult females (18-65 years old) who are scheduled to undergo mastectomy with immediate breast reconstruction surgery will be approached for this study. Those who agree and sign the informed consent form will be randomized in 1:1 fashion (50/50 chance) to either the RPNI group or the no RPNI (Control) group. Study participants will complete self-reported surveys (pre-surgery and at Months 1, 3, 6, and 12 post-surgery) designed to measure pain levels, quality of life, and function before and after surgery. Study participation will last approximately 12 months. Subjects will remain blinded to their assigned study arm until their study participation has concluded.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

盲法说明

Those who agree and sign the informed consent form will be randomized in 1:1 fashion (50/50 chance) to either the RPNI group or the no RPNI (Control) group. Subjects will remain blinded to their assigned study arm until their study participation has concluded.

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Adult female 18 to 65 years of age.
  • Undergoing breast mastectomy with immediate reconstruction.
  • Able to provide informed consent and comply with study procedures.

排除标准

  • History of chronic pain syndrome unrelated to breast surgery.
  • Unwillingness or inability to comply with the study's follow-up requirements.
  • Cognitive impairment or language barriers preventing proper understanding of study procedures and assessments.
  • Participation in other interventional trials or treatments aimed at pain management that could confound study outcomes as determined by the PI.
  • Other medical or surgical contraindication to the involved procedure (RPNI) as determined by the PI.

研究组 & 干预措施

RPNI

Experimental

Subjects will complete BREAST-Q Pre-Op (Qol) survey and Pain Distribution survey prior to Surgery. Subjects will in the RPNI arm will undergo mastectomy with breast reconstruction surgery with regenerative peripheral nerve interface. Subjects will complete BREAST-Q Post-Op (QoL) survey and Pain Distribution Survey at Months 1, 3, 6, and 12 post-surgery. Information about the patient and course of care will be collected from electronic medical records.

干预措施: Regenerative Peripheral Nerve Interface (Procedure)

No RPNI (Control)

No Intervention

Subjects will complete BREAST-Q Pre-Op (Qol) survey and Pain Distribution survey prior to Surgery. Subjects undergo mastectomy with breast reconstruction surgery without regenerative peripheral nerve interface. Subjects will complete BREAST-Q Post-Op (QoL) survey and Pain Distribution Survey at Months 1, 3, 6, and 12 post-surgery. Information about the patient and course of care will be collected from electronic medical records.

结局指标

主要结局

Incidence of neuroma-related PBSPS

时间窗: 12 months

The study's primary endpoint will be the incidence of neuroma-related PBSPS, assessed by comparing the proportion of participants in each group who experience this condition during a follow-up period of 12 months, through review of electronic medical records.

次要结局

  • Quality of Life change(12 months)
  • Safety and Adverse Events(12 months)
  • Pain change(12 months)

研究者

发起方
George Kokosis
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

George Kokosis

Associate Professor

Rush University Medical Center

研究点 (1)

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