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Implementing a Postoperative MIRP (Minimally Invasive Repair of Pectus) Program Via Tele-monitoring

A

Antwerp University Hospital (UZA)

Status

Completed

Conditions

Postoperative Pain
Postoperative Nausea

Treatments

Procedure: Pectus surgery

Study type

Observational

Funder types

Other

Identifiers

NCT03100669
17/08/082

Details and patient eligibility

About

MIRP (Minimally Invasive Repair of Pectus) as surgical correction of pectus excavatum or carinatum is performed to achieve physiological, cosmetic, and psychological benefits for the patient. Surgery is often associated with severe postoperative pain. In this study the researchers want to registrate pain, sleep, nausea/vomiting, and daily activities in short and long term follow up.

Full description

In order to provide pain patients with an individualized approach to their pain problem after MIRP we developed an electronic medical record coupled to a set of telemetric medical-grade devices. Appi@Home (Antwerp Personalized Pain Initiative) supports an innovative approach to (sub)acute conditions by offering a platform for continuous follow-up. Patients are provided with a toolbox and an app that continuously collects objective outcome data (i.e. pain intensity, sleep quality, physical activity). The integrated system allows the care givers to respond very quickly to changing clinical conditions of the patient, making a very adaptive and individualized follow-up possible for these patients. In addition, the patient becomes an active participant in the global therapeutic approach.

Patients receive the toolbox two week prior to surgery with access to the internet platform for questionnaires fill-in procedure. Up to ten week after surgery pain intensity, sleep quality and physical activity will be monitored subjectively by a scoring table (0-10, 0 no pain-bad sleeping quality-no activity, 10 maximum of pain-excellent sleeping quality- a lot of activity) and objectively by blood pressure device, oxygen saturation monitoring, activity tracker and sleep registration tool.

Enrollment

47 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • elective pectus repair
  • signed informed consent

Exclusion criteria

  • chronic opioid use (> 3 months)
  • history of ongoing psychiatric disease

Trial design

47 participants in 1 patient group

Pectus surgery
Description:
Single arm study: patient undergoing pectus repair surgery
Treatment:
Procedure: Pectus surgery

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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