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Postoperative Complications in Patients With Obesity Hypoventilation Syndrome

Postoperative Complications in Patients With Obesity Hypoventilation Syndrome Based on Base Excess- OHBE Study: A National, Multicenter, Observational Cohort Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02980770
Acronym
OHBE
Enrollment
999
Registered
2016-12-02
Start date
2016-11-30
Completion date
2018-06-30
Last updated
2017-04-06

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

Conditions

Acid-Base Imbalance, Hypercapnia, Obesity Hypoventilation Syndrome, Obstructive Sleep Apnea, Post-Op Complication

Keywords

Obstructive Sleep Apnea, Obesity Hypoventilation Syndrome, Hypercapnia, Post-Op Complication, Acid-Base Imbalance

Brief summary

Obstructive sleep apnea (OSA) and Obesity-Hypoventilation Syndrome (OHS) are common conditions in obesity, which may influence the prognosis in patients undergoing surgery. There is a need for simple screening tools to identify such patients at high risk. The current multicenter observational study aims to investigate occurrence of OSA and OHS in obese individuals undergoing elective abdominal surgery and further address its impact on perioperative and postoperative complications.

Detailed description

Obstructive sleep apnea (OSA) and Obesity-Hypoventilation Syndrome (OHS) are common conditions in obesity, which may influence the prognosis in patients undergoing surgery. There is a need for simple screening tools to identify such patients at high risk. The current multicenter observational study aims to investigate occurrence of OSA and OHS in obese individuals undergoing elective abdominal surgery by using questionnaires (STOPBANG questionnaire, Berlin Questionnaire, and Epworth Sleepiness Scale) and arterial blood gases. Perioperative and 72-h postoperative complications will be documented.

Interventions

None listed

Sponsors

Elazig Education and Research Hospital
CollaboratorUNKNOWN
Mustafa Kemal University
CollaboratorOTHER
Aydin Adnan Menderes University
CollaboratorOTHER
TC Erciyes University
CollaboratorOTHER
Sisli Hamidiye Etfal Training and Research Hospital
CollaboratorOTHER
Haydarpasa Numune Training and Research Hospital
CollaboratorOTHER
Fatih Sultan Mehmet Training and Research Hospital
CollaboratorOTHER
Konya Meram State Hospital
CollaboratorOTHER
Ankara City Hospital Bilkent
CollaboratorOTHER
Adana Numune Training and Research Hospital
CollaboratorOTHER_GOV
Tepecik Training and Research Hospital
CollaboratorOTHER
Sakarya University
CollaboratorOTHER
Ankara University
CollaboratorOTHER
Kahramanmaras Sutcu Imam University
CollaboratorOTHER
Trakya University
CollaboratorOTHER
Karadeniz Technical University
CollaboratorOTHER
Dr. Lutfi Kirdar Kartal Training and Research Hospital
CollaboratorOTHER_GOV
Turkiye Yuksek Ihtisas Education and Research Hospital
CollaboratorOTHER_GOV
Ufuk University
CollaboratorOTHER
Kasımpasa Training and Research Hospital
CollaboratorUNKNOWN
Nevsehir Public Hospital
CollaboratorOTHER_GOV
Hitit University
CollaboratorOTHER
Bulent Ecevit University
CollaboratorOTHER
Medipol University
CollaboratorOTHER
Marmara University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Patients undergoing elective abdominal surgery * Body-Mass-Index \>=30 kg/m2 * Ability to read and speak * Signed informed consent.

Exclusion criteria

* Use of diuretics * Use of theophylline * Use of respiratory depressing drugs * Severe lung disease (FEV1/FVC\<%50) * Severe hearth failure (EF\<%35) * Central nervous system or muscle disease * Untreated hypothyroidism * Renal failure (GFR\<50) * Total parenteral nutrition more than 72 hours * Hypokalemia * Hyponatremia * Hypomagnesemia * Hypoalbuminemia * Known sleep apnea or obesity hypoventilation syndrome * Blood transfusion from blood bank within 72 hours prior to surgery

Design outcomes

Primary

MeasureTime frame
Postoperative complications72 hours

Countries

Turkey (Türkiye)

Contacts

Primary ContactIsmail Cinel, Prof Dr
cinelismail@yahoo.com+905324129596
Backup ContactYuksel Peker, Prof Dr
yukselpeker26@gmail.com+905443484866

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026