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Effect of transcutaneous electrical nerve stimulation on postoperative pain in patients after surgical treatment of distal radius fracture.

Physiotherapeutic treatment of patients after radio-distal fracture during the hospital and outpatient phases.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-2gfygv
Enrollment
Unknown
Registered
2018-07-24
Start date
2018-06-01
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

Fracture of the distal end of the radius

Interventions

It will be a prospective, controlled, randomized, double-blind clinical trial including patients undergoing radical radical distal surgery at the Hospital de Clínicas of UFTM. Participants will partic
• visual analogue scale (EVA) (Annex 3), which consists of a wave of 10 centimeters or an individual mark of agreement according to its level, with the zero end corresponding to "no pain" at the end 1
• Catastrophic pain thinking scale (B-PCS) (Annex 4). This scale is translated and validated for Brazilians or Portuguese and reliable research is used to evaluate catastrophization and association wi
Procedure/surgery
E02.331.800
G16.762.891.500

Sponsors

Universidade Federal do Triângulo Mineiro
Lead Sponsor
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
Collaborator

Eligibility

Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Age greater than 18 years; Both sexes, female or male; Subjected to distal radio-fracture surgery with internal fixation that are hospitalized at the UFTM Clinical Hospital; With postoperative pain complaint; Ability to respond to assessment; Ability to sign the TCLE; Absence of: neurovascular lesions; pregnancy or lactation; severe arrhythmia and use of cardiac equipment; history of epilepsy; severe medical illness, such as uremia, decompensated liver cirrhosis and cancer; psychosis unable to cooperate; and experience with TENS.

Exclusion criteria

Exclusion criteria: To present dehiscence or infection in the surgical incision with exposure of the injured skin; New surgery during the period of intervention or death; Neurovascular lesions diagnosed after hospital intervention;

Design outcomes

Primary

MeasureTime frame
As a primary endpoint or direct result, the pain relief of the patients in the postoperative period of Radio Distal Fracture surgeries after the application of TENS is expected.

Secondary

MeasureTime frame
And as a side effect it is expected that it will promote a reduction in the consumption of analgesics aiding in the reduction of symptoms and improvement of the functional capacity. Reducing hospital costs and reducing possible complications.

Countries

Brazil

Contacts

Public Contactluciane;luciane fernandes;fernandes

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior;Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

fernandes.luciane72@gmail.com;fernandes.luciane72@gmail.com+55-034-992622254;+55-034-992622254.

Outcome results

None listed

Source: REBEC (via WHO ICTRP)