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Quantification of Chest Wall Changes After Nuss Bar Removal Utilizing Three-dimensional Optical Surface Scans (CHEST)

Z

Zuyderland Medisch Centrum

Status

Unknown

Conditions

Pectus Excavatum

Treatments

Other: 3D optical surface scan

Study type

Interventional

Funder types

Other

Identifiers

NCT04052321
METCZ20190103

Details and patient eligibility

About

Pectus excavatum is the most common anterior chest wall deformity that affects up to 1:400 of newborns. If an operative correction is indicated, patients are often operated via the Ravitsch or Nuss bar procedure. The latter (i.e. the Nuss bar procedure) is the most commonly performed procedure. During this procedure one or more metal bars are inserted behind the sternum to push the sternum back into its normal position. These bars remain in situ for two-to-three years before being removed. Despite the fact that the Nuss bar procedure is regarded as an effective procedure, retraction may occur after removal. A recent study has investigated this phenomenon, utilizing three-dimensional (3D) optical surface scans acquired before and after Nuss bar removal. The authors found statistically significant changes to occur in chest wall dimensions directly after, as well as between 2 and 8 weeks after Nuss bar explantation, in comparison to the situation just prior to bar removal. They, moreover, found the time the bar was in situ to be predictive for retraction. However, the authors also stressed that further studies are needed to reinforce their preliminary findings and perform long-term assessments. Subsequently, a similar study with long-term assessments will be conducted.

Enrollment

25 estimated patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients that received 1 or more Nuss bar(s) to treat pectus excavatum and is/are scheduled to be removed due to the end of treatment.

Exclusion criteria

  • Patients in which the Nuss bar(s) or its stabilizers are or have been dislocated.
  • Patients that received a second operation to treat any complications regarding the initial Nuss bar implantation.
  • Patients with proven connective tissue diseases (e.g. Marfan's syndrome).
  • Patients with a diagnosis of epilepsy (as the 3D scanner utilizes flashing light to acquire the torso topography)
  • Patients that are not fit to remain in a standing position with their arms above shoulder level for a maximum of 60 seconds.

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

25 participants in 1 patient group

3D scan arm
Experimental group
Description:
This is a single arm study. Patients in this arm will receive a 3D scan just prior to, 2 weeks after, as well as 6 and 12 months after Nuss bar removal.
Treatment:
Other: 3D optical surface scan

Trial contacts and locations

1

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Central trial contact

Jean Daemen

Data sourced from clinicaltrials.gov

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