Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05844800
Other study ID # Maria Jarosz PhD Thesis
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 2011
Est. completion date September 2022

Study information

Verified date March 2023
Source Poznan University of Physical Education
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this study is to determine the effect of Nuss minimally-invasive repair technique of pectus excavatum (PE) on the postural stability in patients with PE. The main questions it aims to answer are: - How surgical chest wall repair will affect postural stability of PE patients? - What is the difference in postural stability between patients with PE and healthy controls? Participants will undergo the Nuss repair surgery and will be tested before and afterwards for their postural stability with the use of the posturography method. Researchers will compare PE male patients and healthy young men to see if PE posture defect affects postural stability.


Description:

The experiment was designed as a pretest-posttest control trial. The clinical examination and surgery intervention (minimally invasive repair of pectus excavatum - MIRPE) of pectus excavatum patients are done in Wielkopolska Centre of Pulmonology and Thoracosurgery in Poznań, Poland. Other postural stability assessment of both, experimental group and control group subjects are done in the Poznań University of Physical Education in Poland. The measurements are carried out twice, before and three months after the intervention for experimental group, and twice for control group as well. Before the experiment initial measurements connected to basic and somatic characteristics assessments are recorded. Participants are also familiarized with measurement methods. All PE patients included in the study after preoperative examination undergo the Nuss surgery procedure (MIRPE): curved metal bars are inserted behind the sternum to correct the shape of the anterior chest wall. The bars are left in situ for three years and then removed. The operation is performed under general anesthesia in a hospital setting. Postural stability as a dependent variable was examined with the use of the posturography method based on the measurement of centre of pressure (COP) displacements. The stabilometric platform CQStab2P in two-plates version (CQ Electronic System, Poland) is used for collecting COP data during trials. The platforms are equipped with strain gauges that facilitated the monitoring of the changes in ground reaction forces. It is connected to a computer equipped with software provided by the manufacturer of the platforms. Based on the data of ground reaction forces the position and displacements of COP are estimated in the software. The sampling frequency of 200 Hz is used during data acquisition. According to producer declaration processing accurancy is equal to 0.1% (12-bit processing, effective 10-bit) during reproduction of statokinesiogram with accurancy of 1 mm with radius fluctuation of 10cm. The force platforms are placed on a hard and flat floor surface. Before the start of the testing procedures, the participants rest in a sitting position for 5 min. During the measurement, only the researcher and the participant are present in the room. Participants need to perform trials in three conditions: 1) double stance with eyes open (EO); 2) double stance with eyes closed (EC); 3) one-leg standing with eyes open (OLS). Each trial is run two times - summing 6 trials in each measurement with a 20-second break between the following trials. The order of trials is random to avoid potential learning effects. An average of two repetitions of specific trials is taken as the final result. The primary outcomes of the study are: 1. Average velocity of COP displacements and its components in anterior-posterior (AP) and medio-lateral (ML) directions (Vavg, VavgAP, VavgML, respectively). It's calculated as a ratio of the total path length covered by COP during the trial, and the time of the trial (mm/s). 2. Indicators of the spatial distribution of COP displacements i.e.sway area (SA) and maximal COP displacementin AP and ML directions (MaxAP and MaxML, respectively). SA is calculated as the size of the area covered by the COP during the trial (mm2). MaxAP and MaxML are calculated as maximal swaydistance (mm) of the COP from the 0.0 point along Y and X axis in Cartesian coordinate system, respectively. Study population is characterized also by age, body weight and height, and body mass index (BMI) - calculated as body weight/height2. The main calculations related to the assessment of the variability of dependent variables are based on the ANOVA variance analysis method (test F). The analysis applied takes into account within-group factor of repeated measurements "time" with two levels (pre and post), and between-group factor "group" (experimental and control). For interaction effects ("group" × "time") the eta-squared effect size is calculated. The effect size indicates the percent of variance explained by particular effects of the dependent variable. To compare the average values of average velocities, area, and maximal COP displacement (both pre-post values within groups, and between groups in pre and post conditions) Bonferroni detailed post-hoc comparisons is used. Between-groups comparison for secondary outcomes in pretest is done with the use of t-Student test. The minimum level of statistical significance was defined as p ≤ 0.05. The study is conducted using the Statistica v. 13.0 software program.


Recruitment information / eligibility

Status Completed
Enrollment 43
Est. completion date September 2022
Est. primary completion date September 2022
Accepts healthy volunteers No
Gender Male
Age group 14 Years and older
Eligibility Inclusion Criteria: - pectus excavatum (experimental group) - no posture defects (control group) - no neurological disorders - consent to the surgical intervention procedure (experimental group) Exclusion Criteria: - co-existence of defects in the anterior chest wall other than pectus excavatum - presence of musculoskeletal anomalies

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Nuss repair of Pectus Excavatum
The Nuss procedure is a minimally-invasive repair technique of PE (MIRPE), whereby one to three curved metal bars are inserted behind the sternum to correct the shape of the anterior chest wall. The bars are left in situ for three years and then removed.
Drug:
Epidural anesthesia
The Nuss procedure of pectus excavatum repair surgery is performed under general anesthesia. Epidural anesthesia, with a constant infusion of 0.25% bupivacaine, was routinely used and was maintained in the early postoperative period.

Locations

Country Name City State
Poland Poznan University of Physical Education Poznan
Poland Wielkopolska Centre of Pulmonology and Thoracic Surgery in Poznan Poznan

Sponsors (2)

Lead Sponsor Collaborator
Poznan University of Physical Education Wielkopolska Centre of Pulmonology and Thoracic Surgery in Poznan

Country where clinical trial is conducted

Poland, 

References & Publications (3)

Blaszczyk JW, Beck M, Sadowska D. Assessment of postural stability in young healthy subjects based on directional features of posturographic data: vision and gender effects. Acta Neurobiol Exp (Wars). 2014;74(4):433-42. — View Citation

de Loos ER, Daemen JHT, Pennings AJ, Heuts S, Maessen JG, Hulsewe KWE, Vissers YLJ. Minimally invasive repair of pectus excavatum by the Nuss procedure: The learning curve. J Thorac Cardiovasc Surg. 2022 Mar;163(3):828-837.e4. doi: 10.1016/j.jtcvs.2020.11.154. Epub 2020 Dec 10. — View Citation

Pawlak K, Gasiorowski L, Gabryel P, Galecki B, Zielinski P, Dyszkiewicz W. Early and Late Results of the Nuss Procedure in Surgical Treatment of Pectus Excavatum in Different Age Groups. Ann Thorac Surg. 2016 Nov;102(5):1711-1716. doi: 10.1016/j.athoracsur.2016.04.098. Epub 2016 Jun 30. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Postural Stability Postural stability as a dependent variable examined with the use of the posturography method based on the measurement of Centre of Pressure displacements. Three months
Secondary BMI Body mass index (BMI) - calculated as body weight/height2 Single measurement
See also
  Status Clinical Trial Phase
Completed NCT05034601 - ESPB vs TPVB for Postoperative Analgesia After the Nuss Procedure N/A
Completed NCT02552186 - Non-invasive Clinical Pectus Index as a Measurement of Severity in Pectus N/A
Recruiting NCT04167865 - Effects of Exercise Therapy on Pectus Excavatum N/A
Completed NCT05443113 - Young Pectus Excavatum Patients and Genetic Defects
Completed NCT04362878 - Psychological Assessment of Patients With Chest Wall Deformities
Recruiting NCT06110689 - Capturing Physiologic Autonomic Data From Clinically Indicated Magnetic Resonance Imaging Scans in Children
Completed NCT02009267 - Nuss Procedure: Clinical Options in Pediatric Pain Management? N/A
Recruiting NCT01486953 - Pulmonary Mechanics During Minimally Invasive Repair of Pectus Excavatum Phase 4
Completed NCT02169297 - Sub-Paraspinal Block in Nuss Patients. A Pilot Project Phase 4
Completed NCT02174796 - Hemodynamic Repercussions of the Correction (Surgical and Non Surgical) of Pectus Excavatum-type Thoracic Deformities N/A
Recruiting NCT04211935 - Identification of Best Postoperative Analgesia Method Following a Minimally Invasive Repair of Pectus Excavatum N/A
Completed NCT02721017 - Cryoanalgesia vs. Epidural in the Nuss Procedure Phase 4
Completed NCT02337621 - Pain, Exercise and Psychological Well-being in Pectus Excavatum
Terminated NCT01863498 - Prospective Trial: Pain Management After Pectus Excavatum Repair, Epidural Versus PCA N/A
Recruiting NCT04418583 - Quantifying the Effect of the Crane Technique Through Three-dimensional Imaging N/A
Active, not recruiting NCT05063695 - Pectus ESC Outcomes and Comparative Effectiveness Study
Completed NCT01816373 - Non-invasive Negative Pressure Treatment for Pectus Excavatum N/A
Withdrawn NCT02376634 - Hypnotherapy in Major Surgical Procedures N/A
Not yet recruiting NCT06436755 - Serratus Anterior Plane Block and Transthoracic Plane Block in Pectus Surgery
Completed NCT02163265 - Impact of Surgical Treatments of Thoracic Deformation on Cardiopulmonary Functions N/A