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Effect of different controlled hypotension technique on important organ function in patients undergoing orthognathic surgery

Effect of different controlled hypotension technique on important organ function in patients undergoing orthognathic surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900024758
Enrollment
Unknown
Registered
2019-07-26
Start date
2019-11-01
Completion date
Unknown
Last updated
2019-10-28

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

Conditions

dentomaxillofacial deformities

Interventions

group A:increase the dose of anesthetic

Sponsors

The Third Affiliated Hospital of the Air Force Military Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Patients scheduled for orthognathic surgery in the department of Oral and maxillofacial surgery of The Third Affiliated Hospital of the Air Force Military Medical University; 2. Proposed surgery: Maxillary LEFORTI osteotomy + mandibular sagittal split surgery + genioplasty (with or without); 3. Aged 18 to 45 years old.

Exclusion criteria

Exclusion criteria: 1. Refused to sign the informed consent; 2. Preoperative SBP=140mmHg and/or DBP=90mmHg; Preoperative SBP=90mmHg and/or DBP=60mmHg; 3. patients with abnormal ECG; 4. patients with abnormal blood routine examination; 5. patients with abnormal coagulation system; 6. patients with abnormal renal function; 7. patients with abnormal Chest X-ray; 8. patients with ASA=II; 9. BMI=27kg/m2.

Design outcomes

Primary

MeasureTime frame
SIRS with brain dysfunction (stroke or postoperative delirium) during 24 hours after surgery;SIRS with renal dysfunction (AKIN: level? or above)during 24 hours after surgery;SIRS with with cardiac dysfunction (arrhythmia or myocardial ischemia or infarction) during 24 hours after surgery;SIRS with pulmonary dysfunction (hypoxemia or pneumonia) during 24 hours after surgery;

Secondary

MeasureTime frame
Incidence of SIRS during 24 hours after surgery;Incidence of brain dysfunction (stroke or postoperative delirium) during 24 hours after surgery;Incidence of acute kidney injury (AKIN: level?or above) during 24 hours after surgery;Incidence of cardiac dysfunction (arrhythmia, myocardial ischemia or infarction) during 24 hours after surgery;Incidence of pulmonary dysfunction (hypoxemia or pneumonia) during 24 hours after surgery;PSI and SR during the operation;HR and BP during the operation;Infusion volume, blood transfusion volume, blood loss volume, urine volume;dose of propofol, sevoflurane,remifentanil and nicardipine;time of controlled hypotension and time of operation;Incidence of PONV during 24 hours after surgery;Time of tracheal tube removal;Time of waking up to steward 6;The time when MAP increased to 65mmHg after the cessation of controlled hypotension;Incidence of postoperative infection;LOS(length of stay);

Countries

China

Contacts

Public ContactZhang Hui

The Third Affiliated Hospital of the Air Force Military Medical University

zhanghuifmmua@163.com+86 029-84776119

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026