Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06759623

Assessment of Pulmonary Function in Relation to the Anesthetic Used in Patients Undergoing Bariatric Surgery

Led by Medical University of Gdansk · Updated on 2025-01-06

100

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the effects of different inhalational anesthetics on lung function in obese patients undergoing bariatric surgery. The study focuses on comparing pulmonary function before anesthesia and after awakening, specifically examining the impact of sevoflurane versus desflurane during general anesthesia. It is known that pulmonary function often declines after anesthesia, and this study aims to clarify how these two anesthetics influence lung function in this patient group. Participants will be randomly assigned to receive general anesthesia with either sevoflurane or desflurane as the volatile agent during their bariatric surgery. The study monitors several anesthesia-related measures continuously during the procedure, including heart rate, oxygen saturation, carbon dioxide levels, and blood pressure. Lung function tests, such as forced vital capacity and peak expiratory flow, will be conducted three months before surgery and at 10 and 30 minutes after awakening from anesthesia. During the study, participants will undergo continuous monitoring of vital signs and anesthesia depth throughout surgery. Lung function assessments will be performed at set times before and after the procedure. Researchers will measure various lung function parameters to evaluate respiratory health changes related to the anesthetic used. The total participation includes preoperative assessments, surgery with monitored anesthesia, and short-term postoperative lung function tests to understand recovery dynamics.

CONDITIONS

Brief Title

Assessment of Pulmonary Function in Relation to the Anesthetic Used in Patients Undergoing Bariatric Surgery

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Obese patients qualified for bariatric surgery
Not Eligible

You will not qualify if you...

  • Patients with absolute contraindications to spirometry testing
  • Patients with aneurysms of the aorta or cerebral arteries at risk of rupture or recent vascular surgery
  • Patients with increased intracranial pressure or recent intracranial bleeding or head surgery
  • Patients with acute conditions within 6 months prior to surgery such as stroke, myocardial infarction, unstable angina, or pneumothorax
  • Patients with uncontrolled hypertension
  • Patients after recent eye surgery or with a history of retinal detachment
  • Patients with hemoptysis of unknown cause
  • Patients unable to perform spirometry testing

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Duration of surgery and anesthesia

Participants undergo bariatric surgery under general anesthesia with either desflurane or sevoflurane. Pulmonary function and vital signs are monitored continuously during anesthesia.

1 surgery visit with continuous monitoring during anesthesia

Follow-up

Duration - 3 months before surgery through immediate post-anesthesia period

Pulmonary function tests are performed 3 months before surgery and repeated 10 and 30 minutes after emergence from anesthesia to assess recovery.

3 visits (1 before surgery, 2 shortly after surgery)

Trial Site Locations

Total: 1 location

1

University Clinical Center

Gdansk, Poland

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Research Team

K

Karolina Obara, MD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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