Actively Recruiting

Age: 0Years - 18Years
All Genders
ID07494370

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

Age: 0Years - 18Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Pediatric patients evaluated at the upper airway endoscopy clinic who are candidates for adenoidectomy
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery and Immediate Post-operative Care

Duration - Up to 1 week

Participants undergo adenoidectomy surgery and receive immediate post-operative care.

1 surgery visit and approximately 2 post-operative visits

Long-term Monitoring

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

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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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