Buccal Fat for Transoral Robotic Lateral Oropharyngectomy Defects to and Postoperative Pain

Phase 2

Not yet recruiting

• Conditions: Tonsil Neoplasm; Oropharynx Neoplasm; Transoral Robotic Surgery

• Registration Number: NCT06965738
• Lead Sponsor: University Health Network, Toronto

Brief Summary

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.

Detailed Description

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.

Study Timeline

• Study First Submitted: 2025-03-31
• Status Verified: 2025-05
• Study First Submitted QC: 2025-05-01
• Study First Posted: 2025-05-11
• Last Update Submitted: 2025-05-19
• Last Update Posted: 2025-05-21
• Study Start: 2025-06-01
• Primary Completion: 2027-04-01
• Study Completion: 2027-05-01

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

1. Age > 18

2. 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

3. Ability to understand and willing to sign a written informed consent

Exclusion Criteria

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Postoperative pain during rest and swallowing	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

Secondary Outcome Measures

Name	Time	Method
Surgical Complications	30 days postoperatively	Surgical complications and adverse events within 30 days postoperatively using the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTC-AE v4.0)
Opioid usage	30 days postoperatively	Determine opioid usage
Postoperative Hemorrhage	30 days postoperatively	Postoperative hemorrhage after TORS
Speech and Swallowing	Once each at the following timepoints: 1-2 week preoperatively, postoperative day 7-10, postoperative day 21-28	Determine postoperative speech and swallowing using the Performance Status Scale for Head and Neck (PSS-HN)
Oral Diet	Once each at the following timepoints: 1-2 week preoperatively, postoperative day 7-10, postoperative day 21-28	Determine food consistencies achieved at short post-operative follow up (per PSS-HN)
Feeding Tube Placement	30 days postoperatively	Determine rate of feeding tube placement
Blood Glucose	30 days postoperatively	Determine blood glucose levels

Trial Locations

Locations (1)

Toronto General Hospital; 🇨🇦 Toronto, Ontario, Canada