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A Review of Surgical Management of Congenital Pulmonary Airway Malformations (CPAM): A Decade of Experience

NCT04449614 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 72

Last updated 2020-06-29

No results posted yet for this study

Summary

Congenital pulmonary malformation in children is a rare abnormality mostly diagnosed before birth during antenatal ultrasound examinations. These lesions may expand to form lung cysts in children, cause recurrent lung infections and has a potential for malignant change. Therefore, surgical removal in childhood is favoured as the treatment of choice.

The surgical correction may involve 'open' surgery or 'key hole' surgery. There is, however, a variation in surgical and anaesthetic techniques and timing of this surgery and subsequent complications reported post-surgery.

The purpose of this investigation is to review anaesthetic and surgical case notes and the subsequent well-being of all children who underwent lung surgery to remove above lung lesions over the last 10 years (2008-2017) at a regional centre. The aim is to look at the current status of these children in relation to their health, growth and development evaluated via a 20-minute structured telephone interview with prior consent.

Conditions

  • Pulmonary Arteriovenous Malformation
  • Congenital Disorders

Interventions

PROCEDURE

Thoracoscopic CPAM resection

Surgical removal of lung lesion

Sponsors & Collaborators

Principal Investigators

  • Chulananda Goonasekera · Consultant Anaesthetist

Eligibility

Max Age
16 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-01-10
Primary Completion
2019-09-30
Completion
2020-02-28

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04449614 on ClinicalTrials.gov