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NCT06943703Completed

Bleomycin as an Effective and Curative Adjunct Therapy for Lymphangioma

Safety, Efficacy, and Long-Term Outcomes of Intralesional Bleomycin Injection as an Adjunctive Therapy for Pediatric Lymphatic Malformations: A Retrospective Study on Cosmetic and Health-Related Quality of Life Improvements.

Source: ClinicalTrials.gov · Last updated 24 Apr 2025

Brief summary (registry, in English)

Lymphatic malformations (LM), or lymphangiomas, are common vascular anomalies in children, most often occurring in the head and neck, less commonly in the axilla, abdomen, thorax, groin, and extremities. These benign but locally invasive lesions can cause complications such as respiratory issues, difficulty swallowing, nerve compression, bleeding, and cosmetic disfigurement. Treatment traditionally involves surgical excision, but this approach carries risks such as nerve damage, high recurrence, and poor cosmetic results. In recent years, sclerotherapy, specifically Bleomycin injection, has emerged as a less invasive alternative, offering potential benefits like reduced recurrence and better cosmetic outcomes. Since its introduction in Vietnam in 2016, Bleomycin has been used to treat LM, but comprehensive studies on its safety, efficacy, and long-term outcomes in pediatric patients are lacking. This study aims to fill this gap by evaluating the effectiveness of intralesional Bleomycin injections in children with LM treated at the National Children's Hospital between 2018 and 2022. The study will assess the safety, efficacy, and long-term outcomes of Bleomycin, focusing on lesion size reduction, recurrence rates, and cosmetic and health-related quality of life (QoL) improvements. The retrospective study will involve more than 800 pediatric patients and use tools like the Patient Scar Assessment Questionnaire (PSAQ) and Short Form-36 (SF-36) health survey to evaluate cosmetic outcomes and overall well-being. The research will also compare the effectiveness of Bleomycin alone versus in combination with surgery, examining whether Bleomycin can reduce the need for additional interventions. By offering a comprehensive evaluation of both clinical and patient-reported outcomes, the study aims to establish Bleomycin as a viable, minimally invasive treatment option for pediatric LM, improving both clinical and cosmetic outcomes for these patients. In addition, this study will provide valuable local data on Bleomycin's use in Vietnam, potentially influencing national treatment guidelines. The results will be disseminated in peer-reviewed journals, contributing to global understanding of Bleomycin's role in managing lymphatic malformations in children.

Status (registry)
Completed
Study type
Observational
Enrollment
809 (actual)
First submitted
6 Apr 2025
Start date
1 Jan 2018
Primary completion date
31 Dec 2022
Lead sponsor
National Children's Hospital, Vietnam
NCT number
NCT06943703

What you commit to

  • Study type: Observational
  • Participants enrolled: 809
  • From 1 Jan 2018 to the primary completion date, 31 Dec 2022
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Other Treatments: Patients who have received prior treatments with Bleomycin for lymphangioma.

Other illness

  • Severe Comorbidities: Presence of serious comorbidities (e.g., uncontrolled cardiovascular disease, active infections) that may interfere with the study or treatment process.
  • Allergy: Known allergy or hypersensitivity to Bleomycin or any of its components.
  • Active Infections: Patients with active local or systemic infections at the time of enrollment.
  • Immunosuppression: Immunocompromised patients (due to illness or medications).

Age

  • Age: Patients over the age of 18 years.

Other

  • Pregnancy: Pregnant or breastfeeding patients.

Who the study is looking for

  • Age: Pediatric patients under the age of 18 years.
  • Diagnosis: Confirmed diagnosis of lymphangioma (lymphatic malformation).
  • Location of Lesions: Lymphangiomas located in the head and neck, axilla, abdomen, thorax, groin, or extremities.
  • Treatment History: No prior treatment with Bleomycin for lymphangioma.
  • Health Status: No serious comorbidities or medical conditions that could interfere with the study or treatment process.
  • Informed Consent: Patients (or their legal guardians) provide informed consent to participate in the study.

Age in the registry: - to 18 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Department of Surgery, The National Children Hospital, Hanoi
Coordinator of this site? Confirm its status
HanoiVietnamUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.