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Mechanical vibration used in Vibratory Platform after cardiac surgery.

Use of Mechanical Vibration Generated in Oscillating/Vibratory Platform in the Post-Operative Heart Surgery.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-3tgsqp
Enrollment
Unknown
Registered
2017-06-26
Start date
2017-08-12
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atherosclerotic cardiovascular disease

Interventions

Intervention group: 25 patients who will undergo cardiac surgery, both valvular and myocardial revascularization. They will begin treatment on the vibratory platform from the fourth postoperative day.
Device
Other
E02.190.525.186

Sponsors

Hospital Universitário da Universidade Federal do Maranhão
Lead Sponsor
Hospital Universitário da Universidade Federal do Maranhão
Collaborator

Eligibility

Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients undergoing cardiac surgery; Both genes; Age between 18 and 80.

Exclusion criteria

Exclusion criteria: Patients who die in the perioperative period Patients who develop pulmonary or neurological complications that impede the evaluations.

Design outcomes

Primary

MeasureTime frame
Expected 1 Recovery of lung function Verified by spirometry From a variation of at least 5% verified in the preoperative and on the sixth postoperative day.;Expected 2 Maintenance of peripheral muscle strength after six days of training. Verified using the handheld hydraulic dynamometer. From a variation of at least 5% in the measurements performed in the preoperative and sixth postoperative day.;Expected 3 Maintenance of functional capacity, after six days of training. checked using the Time Up and Go (TUG) test. From a variation of at least 5% in the preoperative and the sixth postoperative day.;Expected 4 Recovery of inspiratory muscle strength after six days of training. Verified using the digital manovacuometer. From a variation of at least 5% in the preoperative and sixth postoperative day.;Expected 5 Recovery of functional capacity after six days of training. Verified by functional independence measure scale (MIF). From a variation of at least 5% in the measurements performed in the preoperative and sixth postoperative days

Secondary

MeasureTime frame
No secondary outcomes are expected at the end of the study.

Countries

Brazil

Contacts

Public ContactJoão Vyctor Fortes

Hospital Universitário da Universidade Federal do Maranhão

vyctorfortes@yahoo.com.br+55 (98) 2109-2100

Outcome results

None listed

Source: REBEC (via WHO ICTRP)