Actively Recruiting
Adenoidectomy: Correlation Between Individual Factors, Surgical Technique, and Residual Adenoids
Led by Fondazione IRCCS Policlinico San Matteo di Pavia · Updated on 2026-03-27
1200
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Adenoidectomy is the most common ear, nose, and throat surgery performed in children to remove lymphoid tissue from the nasopharynx and open the nasal airways. This procedure usually improves symptoms and quality of life, but some children may experience symptoms again due to leftover or regrown lymphoid tissue, which sometimes requires another surgery. The study aims to understand if individual patient factors like sex, age, weight, height, and soft palate length affect how well the traditional adenoidectomy technique removes this tissue. The traditional adenoidectomy is done without directly seeing the surgical area, often using instruments like an adenoid curette or Shambaugh adenotome. This method can sometimes leave residual tissue behind, which may cause symptom recurrence. This study observes pediatric patients undergoing this traditional surgical technique to evaluate how anatomical and individual factors relate to the completeness of tissue removal. Participants are children evaluated for adenoidectomy and followed for up to five years to assess surgical outcomes related to anatomical factors. Researchers will collect data on these patient-specific characteristics and monitor the presence of residual adenoid tissue after surgery. The main outcome measured is how these anatomical factors influence the success of the surgery over time, helping to clarify reasons behind tissue persistence or regrowth after the procedure.
CONDITIONS
Brief Title
Adenoidectomy: Correlation Between Individual Factors, Surgical Technique, and Residual Adenoids
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pediatric patients evaluated at the upper airway endoscopy clinic who are candidates for adenoidectomy
You will not qualify if you...
History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 1 week
Participants undergo adenoidectomy surgery and receive immediate post-operative care.
1 surgery visit and approximately 2 post-operative visits
Duration - Up to 5 years
Participants are monitored to assess the influence of anatomical factors on surgical outcomes.
Periodic follow-up visits as scheduled by the clinic
Trial Site Locations
Total: 1 location
1
Fondazione IRCCS Policlinico San Matteo di Pavia
Pavia, Lombardy, Italy, 27100
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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