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Evaluation of the use of nasal cannula after the correction surgery of facial discrepancies: passage of air and patient's discomfort

Evaluation of the Nasal Cannula after Orthognathic Surgery: Nasal Airway Permeability and Patient Discomfort

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-57gtfg
Enrollment
Unknown
Registered
2018-05-01
Start date
2017-09-20
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

Respiratory discomfort in patients in the immediate postoperative period of orthognathic surgery Orthognathic Surgery

Interventions

Patients who agree to participate in the study will be randomly divided into two groups. The experimental group will consist of 15 patients of both sexes, where they will undergo orthognathic surgery
Device
Procedure/surgery
E06.892.500
E01.370.386.740
E02.041

Sponsors

Hospital de Reabilitação de Anomalias Craniofaciais
Lead Sponsor
Hospital de Reabilitação de Anomalias Craniofaciais
Collaborator

Eligibility

Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: In this study, 30 patients with repaired cleft palate and / or lip submitted to orthognathic surgery with Le Fort I type osteotomy and bilateral mandibular sagittal osteotomy performed by a single mandibular maxillofacial surgeon from the Hospital for the Rehabilitation of Anomalies Craniofacial of the University of São Paulo (HRAC / USP) of Bauru-SP. Age between 18 and 45 years.

Exclusion criteria

Exclusion criteria: Present cognitive deficit according to medical records; To present important intraoperative events in the intraoperative period and the first 24 postoperative hours, such as: Bleeding; Duration of surgery beyond 3 hours; Unwanted jaw fracture; Airway of difficult intubation (malampat 4, short neck, severe jaw deficiency, deficiency in cervical extension and difficulty in visual access of epiglottis in intubation); Selective intubation; Pulmonary problems due to intubation (pulmonary auscultation suggestive of atelectasis and barotraumas).

Design outcomes

Primary

MeasureTime frame
Difference, in the immediate postoperative period, between the recovery of patients with nasopharyngeal cannula use and without the use of it. Regarding discomfort and permeability, the evaluations were performed in two different moments (6 and 24 hours postoperatively), through rhinomanometry, mirror test and visual analogue ladder.—

Secondary

MeasureTime frame
No side effects expected—

Countries

Brazil

Contacts

Public ContactMaycon Jordão

Hospital de Reabilitação de Anomalias Craniofaciais

mayconjordao@usp.br+55 14 998198968

Outcome results

None listed

Source: REBEC (via WHO ICTRP)