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Percutaneous Peristyloid Glossopharyngeal Block After Tonsillectomy

Comparison Between Two Techniques of Percutaneous Peristyloid Glossopharyngeal Block as an Analgesic Tool After Tonsillectomy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04970680
Enrollment
84
Registered
2021-07-21
Start date
2019-02-01
Completion date
2022-07-30
Last updated
2022-09-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Pain

Keywords

analgesia, tonsillectomy

Brief summary

Adenotonsillectomy surgery in paediatrics is commonly managed as an ambulatory surgery. This may be attributed to the use of the electro-dissection surgical technique that decreases the incidence of immediate postoperative haemorrhage. However, the use of the electro-cautery technique increases postoperative inflammation. This study aimed to compare the glossopharyngeal nerve block using the blind technique with the use of the ultrasound guidance Primary: FLACC score in the two groups 0,2,4,6 h after surgery at rest and with swallowing Secondary: need to analgesics, the difficulty of the technique, time consumption, recovery time, surgeon satisfaction, parents satisfaction, staff nurse satisfaction, anaesthetist self-confidence

Detailed description

INTRODUCTION Adenotonsillectomy surgery in paediatrics is commonly managed as an ambulatory surgery. This may be attributed to the use of the electro-dissection surgical technique that decreases the incidence of immediate postoperative haemorrhage. However, the use of the electro-cautery technique increases postoperative inflammation. Sensory fibres of the glossopharyngeal nerve supply the tonsillar and peri-tonsillar areas. Thus, a bilateral glossopharyngeal nerve block may alleviate post-tonsillectomy pain and improve postoperative analgesia. This is a Prospective randomized controlled clinical study, to compare two different technique used to block the glossopharyngeal nerve. AIM OF WORK To improve post tonsillectomy pain control in children Anaesthesia, postoperative analgesia Paediatrics 3-7 years Tonsillectomy NOT adenotonsillectomy Postoperative control of pain OBJECTIVES This study aimed to compare the glossopharyngeal nerve block using the blind technique with the use of the ultrasound guidance Primary: FLACC score in the two groups 0,2,4,6 h after surgery at rest and with swallowing Secondary: need to analgesics, the difficulty of the technique, time consumption, recovery time, surgeon satisfaction, parents satisfaction, staff nurse satisfaction, anaesthetist self-confidence METHODOLOGY 54 ASA I children allocated randomly into two groups: Group BL: Blind percutaneous peristyloid injection Group US: ultrasound-guided percutaneous peristyloid glossopharyngeal nerve block 54 children aged 3 to 7 years undergoing adenotonsillectomy without adenoidectomy were randomized to receive either local blind percutaneous peistyloid glossopharyngeal nerve block (n=27) or the use of ultrasound guidance for the same block (n=27). The pain was assessed by the FLACC scale or Face, Legs, Activity, Cry, Consolability scale, need for analgesics, and acceptance of diet during the postoperative period.

Interventions

glossopharyngeal nerve block either blindly or using the ultrasonic technique

Sponsors

Suez Canal University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Masking description

the participant will have the block while anaesthetized, the care provider will do the block either blindly or using ultrasonic, the outcome assessor will not know which one have which technique

Intervention model description

two groups, each will have peristyloid glossopharyngeal block, one with the help of ultrasound technology and the other blindly

Eligibility

Sex/Gender
ALL
Age
3 Years to 7 Years
Healthy volunteers
No

Inclusion criteria

* children aged 3-7 years * scheduled for tonsillectomy

Exclusion criteria

* younger or elder children * associated adenoidectomy * history of allergy to local anaesthetics

Design outcomes

Primary

MeasureTime frameDescription
change in face, legs, activity, cry, and consolability (FLACC) scoreImmediately postoperatively considered as 0 hour, then at 2 hours, again at 4 hours, and lastly at 6 hours after surgery all measures will be both at rest and with swallowingFLACC is a behavioural pain assessment scale used for nonverbal or preverbal patients who cannot self-report their pain level. Pain is assessed through observation of 5 categories including the face, legs, activity, cry, and consolability. The scale ranges from 0 to 10 where 0 records for no pain and 10 records for the worst pain

Secondary

MeasureTime frameDescription
difficulty of the techniqueimmediately after the interventionprescribed by the operator either easy or difficult
time consumptionimmediately after the interventionfrom the start of preparation of the procedure, till the end of the block time in minutes
recovery timeimmediately before shifting the patient to recovery roomfrom the end of the surgery, till shifting the patient from operation table to recovery bed time in minutes
need for postoperative analgesiaimmediately postoperatively considered as 0 hour, then at 2 hours, again at 4 hours, and lastly at 6 hours after surgeryneed to analgesics in doses and frequencies both at rest and with swallowing.
anesthetists self-confidenceimmediately after the interventiondescribed as yes or no
parents satisfactionimmediately before discharging the patient to homedescribed by the parents on a scale ranging from very satisfactory to unsatisfactory
staff nurse satisfactionimmediately before shifting the patient from the recovery room to the day care unite by recovery nurse, and immediately after discharging the patient to home by daycare unite nursedescribed by the recovery nurse and daycare unite nurse on a scale ranging from very satisfactory to unsatisfactory
surgeon satisfaction assessed by visual analogue scale (VAS)immediately after discharging the patient to homedescribed by the surgeon him self on a scale ranging from very satisfactory to unsatisfactory

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026