Last updated: November 8, 2023
Sponsor: National Cancer Institute, Egypt
Overall Status: Active - Recruiting
Phase
N/A
Condition
Oral Cavity Cancer
Human Papilloma Virus (Hpv)
Acute Pain
Treatment
Standard voltage pulsed radiofrequency glossopharyngeal nerve block
Supervoltage pulsed radiofrequency glossopharyngeal nerve block
Clinical Study ID
NCT06121102
2203-301-013
Ages 18-70 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Age ≥ 18 and ≤ 70 Years.
- Both sexes
- American Society of Anesthesiologists (ASA) class II and III.
- Patients under pain management for oropharyngeal cancer (failed medical treatment orintolerance to the side effects of the drug).
- Visual analog scale (VAS) equal to or more than 6 cm in spite medical treatment.
Exclusion
Exclusion Criteria:
- Patient refusal.
- Patients with local or systemic sepsis.
- Uncorrectable coagulopathy.
- Unstable cardiovascular disease.
- History of psychiatric and cognitive disorders.
- Patients allergic to medication used.7
- Unable to lie supine.
- Local anatomical distortion (either congenital, post-surgical or post-radiotherapy)making intervention difficult and hazardous.
- Elongated styloid process > 25 mm.
- Age less than 18 year and more than 70 year.
Study Design
Total Participants: 60
Treatment Group(s): 2
Primary Treatment: Standard voltage pulsed radiofrequency glossopharyngeal nerve block
Phase:
Study Start date:
November 08, 2023
Estimated Completion Date:
April 01, 2024
Study Description
Connect with a study center
Cairo University
Cairo, 11796
EgyptActive - Recruiting
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