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Effect of intralesional bevacizumab injection on disease recurrence in children with recurrent laryngeal papillomatosis

Evaluation of the Effect of Intralesional Bevacizumab Injection on Recurrence Frequency and Histopathological Factors Associated with It in Children with Recurrent Laryngeal Papillomatosis:a case series study

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
IRCT
Registry ID
IRCT20251230068497N1
Enrollment
15
Registered
2026-01-24
Start date
2026-01-30
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Recurrent laryngeal papillomatosis (juvenile-onset recurrent respiratory papillomatosis), a benign HPV-related disease of the larynx characterized by recurrent papillomatous lesions requiring repeated surgical interventions.. Benign neoplasm of larynx

Interventions

Intervention group: Intervention group: Intralesional bevacizumab injection as an adjuvant to standard surgical debulking for recurrent laryngeal papillomatosis in children.

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 18 Years

Inclusion criteria

Inclusion criteria: Children aged =18 years Confirmed diagnosis of recurrent laryngeal papillomatosis based on clinical and/or histopathological findings History of recurrent disease requiring repeated surgical intervention Candidate for surgical debulking with intralesional bevacizumab injection Written informed consent obtained from parents or legal guardians

Exclusion criteria

Exclusion criteria: Known hypersensitivity or contraindication to bevacizumab Presence of uncontrolled bleeding disorders Severe concomitant systemic disease precluding surgery or anesthesia Incomplete medical records or inability to complete follow-up Concomitant use of other adjuvant therapies affecting recurrence rate (if applicable)

Design outcomes

Primary

MeasureTime frame
Time to first recurrence of laryngeal papillomatosis after intralesional bevacizumab (adjuvant to surgical debulking). Timepoint: From the date of intervention to the date of first documented recurrence, assessed during follow-up (up to 12 months). Method of measurement: Recurrence will be determined by clinical assessment and endoscopic laryngeal examination (and operative findings if re-intervention is required). Dates of intervention and first confirmed recurrence/need for repeat surgery will be recorded to calculate the interval.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactArya jafari

Iran University of Medical Sciences

Jafari.arya@iums.ac.ir+98 21 6435 1000

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 7, 2026