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临床试验/NCT06965738
NCT06965738尚未招募2 期

Buccal Fat Applied to Transoral Robotic Lateral Oropharyngectomy Defects to Lessen Radical Tonsillectomy Pain (BOLT)

University Health Network, Toronto1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年6月1日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
尚未招募
入组人数
40
试验地点
1
主要终点
Postoperative pain during rest and swallowing

研究概览

简要总结

The goal of this randomized clinical trial is to determine the pain intensity during rest and swallowing in patients undergoing transoral robotic surgery for tonsil lesions with and without buccal fat reconstruction. The main question it aims to answer is: does buccal fat after transoral robotic surgery reduce pain after surgery? Additional questions to be explored include if there is a difference in swallowing, complication rates, pain medication usage, and feeding tube usage. Participants will be asked to rate their pain and swallowing on a visual analogue scale after surgery. The group will be compared compared to a control group that undergoes transoral robotic surgery without buccal fat reconstruction.

详细描述

Trans-oral robotic surgery (TORS) for oropharyngeal cancers have transformed how oropharyngeal cancers are managed, allowing for minimally invasive surgical access to remove tumors of the tonsil and base of tongue. While large incisions and open approaches can be avoided, oropharyngeal defects following TORS are traditionally left as an open wound to heal by secondary intention, resulting in significant postoperative pain, and possibly dysphagia and dehydration.

While this has been highlighted as a key outcome measure, studies on acute pain following TORS have not had any standardization regarding the timing of pain measurement, and pain assessment. Only one study has assessed pain during 'movement-related pain', such as swallowing, which has been advocated as a key metric. Most studies used a visual analogue scale, however, majority failed to describe the timing of pain assessment relative to administration of analgesia, time of day, or diet. Overall, pain ratings and opioid utilization were highly variable between studies resulting in pain ratings ranging widely from 2.5-8 in the first few days postoperatively.

Based on the current evidence, multimodal analgesia resulted in the lowest pain ratings following TORS, with those that included gabapentin, a COX-2 inhibitor and acetaminophen having excellent pain control in the early postoperative period. Using these regimens, Castellanos et al. found that postoperative opioid consumption significantly decreased in the first three postoperative days. Clayburgh, et al. identified that addition of perioperative corticosteroids was safe and significantly improved diet consistency, and decreased length of hospital stay, though pain scores were minimally affected.

No study thus far has assessed the impact of surgical interventions on postoperative pain and swallowing. This single center, phase II, randomized control trial aims to evaluate the impact of the buccal fat rotational flap on the postoperative pain following TORS.

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
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
否

入选标准

  • •Require a transoral robotic lateral oropharyngectomy as a result of the following conditions :
  • •Early - intermediate stage tonsillar squamous cell carcinoma (T1-2N0-1 p16+/- SCC of the palatine tonsils)
  • •Early -intermediate stage salivary gland tumors of the palatine tonsils
  • •based on FNA, Core biopsy, Punch biopsy
  • •Ability to understand and willing to sign a written informed consent

排除标准

  • •History of prior head and neck squamous cell carcinoma, or prior head and neck radiotherapy
  • •Presence of retropharyngeal lymphadenopathy
  • •Presence of bilateral lymphadenopathy, or patients requiring bilateral neck dissections.
  • •Patients with trismus at baseline
  • •Patients with psychological risk factors for persistent opioid use or drug addiction
  • •Need for open surgery (transcervical lateral oropharyngectomy), free tissue transfer, or alternative regional flap.

研究组 & 干预措施

Transoral lateral oropharyngectomy alone

Active Comparator

Transoral lateral oropharyngectomy without buccal fat reconstruction

干预措施: No buccal fat reconstruction (Procedure)

Transoral lateral oropharyngectomy with buccal fat reconstruction

Experimental

Transoral lateral oropharyngectomy with buccal fat reconstruction

干预措施: Buccal fat reconstruction (Procedure)

结局指标

主要结局

Postoperative pain during rest and swallowing

时间窗: Once each at the following timepoints: 1-2 week preoperatively, postoperative day 1-3, postoperative day 7-10, postoperative day 21-28

Postoperative pain during rest and swallowing on visual analogue scale at multiple time points

次要结局

  • Surgical Complications(30 days postoperatively)
  • Opioid usage(30 days postoperatively)
  • Postoperative Hemorrhage(30 days postoperatively)
  • Speech and Swallowing(Once each at the following timepoints: 1-2 week preoperatively, postoperative day 7-10, postoperative day 21-28)
  • Oral Diet(Once each at the following timepoints: 1-2 week preoperatively, postoperative day 7-10, postoperative day 21-28)
  • Feeding Tube Placement(30 days postoperatively)
  • Blood Glucose(30 days postoperatively)

研究者

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

Christopher Yao

Principal Investigator

University Health Network, Toronto

研究点 (1)

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