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Postoperative Pulmonary Complications In Obstructive Sleep Apnea Patients

NCT06041750 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 500

Last updated 2023-09-18

No results posted yet for this study

Summary

It is known that perioperative respiratory complications occur more often in obstructive sleep apnea syndrome (OSAS) patients during general anesthesia. Although there are prospective RCTs in this area, the need for further and larger studies remains due to the heterogenity of the results. Moreover, the incidence of postoperative pulmonary complications in OSAS patients undergoing surgery in Turkey and the predictive factors affecting the respiratory adverse events are uncertain. Therefore, in this prospective observational cohort study, it was aimed to determine the incidence of postoperative pulmonary complications and the predictor factors associated with patient, anesthesia and surgery in surgical patients with a confirmed or highly suspected OSAS diagnosis undergoing general anesthesia.

Conditions

Interventions

PROCEDURE

Elective surgical procedure under general anesthesia

The incidence of postoperative pulmonary complications in OSAS patients undergoing elective surgery under general anesthesia will be determined.

Sponsors & Collaborators

  • Istanbul University - Cerrahpasa

    collaborator OTHER

  • Acibadem University

    collaborator OTHER

  • Baskent University

    collaborator OTHER

  • Celal Bayar University

    collaborator OTHER

  • Cukurova University

    lead OTHER

Principal Investigators

  • Çiğdem Tütüncü, Prof. Dr. · İstanbul University, Cerrahpaşa, Faculty of Medicine

  • Demet Laflı Tunay, Dr. · Çukurova University, Faculty of Medicine

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-10-15
Primary Completion
2024-12-15
Completion
2025-03-31

Countries

  • Turkey (Türkiye)

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06041750 on ClinicalTrials.gov