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临床试验/NCT05200806
NCT05200806招募中4 期

A Prospective Pilot Study of a Non-Narcotic Post-Operative Course After Colectomy

University of Vermont1 个研究点 分布在 1 个国家目标入组 25 人开始时间: 2022年2月7日最近更新:
适应症
干预措施

试验速览

阶段
4 期
状态
招募中
入组人数
25
试验地点
1
主要终点
Failure Rate

研究概览

简要总结

With this pilot investigation, the investigators aim to challenge the reliance on opiate analgesia following colon and rectal surgery. Narcotic misuse and abuse is a pressing public health concern, and reduction in prescription rates could help to mitigate this issue. The goal of this pilot study is to establish feasibility of sufficient post-operative pain control after colectomy using non-narcotic analgesics. The investigators hypothesize that patients will be able to manage their post-operative pain without narcotic intervention, while minimizing side effects and complications. This initial pilot study will provide proof-of-concept for a larger, randomized investigation on non-narcotic analgesia after colectomy.

详细描述

Our primary objectives are:

  • Determine the rate of patients needing rescue narcotics prescriptions for breakthrough postoperative pain after colectomy while on a non-narcotic postoperative protocol.
  • Search for patterns pain and in timing of need for narcotic medication (e.g. in PACU, after intrathecal morphine wear off, etc.)

Secondary objectives:

  • Measure patient satisfaction with pain management via survey administered at discharge and during the 30 days post-operation. This will include questions regarding medication side-effects.
  • Determine factors that may affect patient need for narcotic pain medication, including complications (return to OR, anastomotic leak, prolonged ileus, post-operative hemorrhage), return of bowel function, side effects of medications, and length of hospital stay, which will be taken from patients' charts and surveys for analysis.

Procedures:

研究设计

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

入排标准

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

入选标准

  • •≥ 18 years of age
  • •Undergoing elective abdominal colectomy
  • •Eligible for the Enhanced Recovery After Surgery (ERAS) protocol currently in place for colectomy patients at UVMMC

排除标准

  • •allergy to any protocol medication
  • •emergent or urgent bowel surgery
  • •pre-operative plan for a stoma
  • •pre-operative diagnosis of rectal cancer (pre-operative diagnosis of rectosigmoid cancer is not necessarily excluded)
  • •neoadjuvant chemoradiation
  • •additional malignant disease outside of the colon
  • •narcotic usage within the three months of scheduled operation date, for more than one week
  • •chronic pain
  • •pain score >2 at the initial evaluation for study inclusion
  • •Note: Eligibility will be determined by the research coordinator and approved by the surgeon

研究组 & 干预措施

Intervention

Other

Pre-Op Enhanced Recovery After Surgery (ERAS): Gabapentin (900mg capsule), Acetaminophen (1,000mg tablet), Dexamethasone (8mg IV), Granisetron (1mg IV), Morphine (0.15mg Intrathecal) Intraoperatively: Appropriate medications administered at discretion of the treating anesthesiologist during colectomy, with Ketamine use encouraged if not contraindicated. Post-Op (PACU, Onward during inpatient stay): Acetaminophen (Oral) (650mg, q4hrs), Gabapentin (300mg, q6hours), Methocarbamol (750mg, QID), 5% Lidocaine Patch (q12hrs PRN) One time rescue dose (Hydromorphone, Morphine, Oxycodone) available for breakthrough pain during hospital stay (differs from traditional ERAS protocol where medications can be administered as needed). If one-time rescue dose is needed, the covering physician will be notified and can choose to order an appropriate narcotic regimen for remainder of patient's hospitalization. All patients are discharged with a narcotics prescription that they can choose to fill.

干预措施: Non-Narcotic ERAS Post-Operative Pain Management (Other)

结局指标

主要结局

Failure Rate

时间窗: Until post-op clinic visit (estimated 3-4 weeks post-op)

Need for rescue narcotics for inadequately controlled pain as indicated in Electronic Medical Record (EMR).

次要结局

  • Patient Satisfaction(Until post-op clinic visit (estimated 3-4 weeks post-op))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Peter Cataldo, MD

Colon and Rectal Surgeon, General Surgeon, Professor of Surgery

University of Vermont

研究点 (1)

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