Evaluating ultrasound methods to prevent lung collapse after abdominal surgery
Ultrasound Evaluation of Different Preventive Measures of Post Operative Lung Atelectasis After Upper Abdominal Surgeries: Ventilation and Fluid Measures
This study is testing different ultrasound-guided methods to see if they can help prevent lung collapse in patients having elective abdominal surgery.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 60 (estimated) |
| Ages | 30 Years to 60 Years |
| Sex | All |
| Sponsor | Al-Azhar University Academic / other |
| Locations | 1 site (Assiut) |
| Trial ID | NCT06654778 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to assess the effectiveness of various ultrasound-guided preventive measures for postoperative lung atelectasis in patients undergoing elective abdominal surgeries. The study will utilize a prospective randomized blinded design to evaluate interventions such as positive end-expiratory pressure (PEEP), lung recruitment maneuvers (RM), and restrictive fluid management (RF). By monitoring lung function through ultrasound, the trial seeks to identify the best combination of these measures to reduce the incidence of lung collapse after surgery.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 30-60 with ASA physical status I or II, scheduled for elective abdominal surgeries, and with a BMI under 40.
Not a fit: Patients with a history of chest disorders, psychiatric disorders, or those classified as ASA physical status III or higher may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could significantly reduce the occurrence of postoperative lung atelectasis, leading to improved recovery and outcomes for patients undergoing abdominal surgery.
How similar studies have performed: While there have been studies exploring preventive measures for postoperative lung atelectasis, the specific use of ultrasound evaluation in this context is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * ASA physical status I or II, of either gender. * BMI \< 40 * Age 30-60 years * scheduled for elective abdominal surgeries Exclusion Criteria: * Patient refusal * American Society of Anesthesiologists (ASA) physical status classification system more than II * BMI \> 40 . * Psychiatric disorders * History of chest disorders such as asthma and obstructive pulmonary disease (COPD). * History of Previous Thoracic Procedures. * Pregnancy
Where this trial is running
Assiut
- Al-Azhar university — Assiut, Egypt (Recruiting)
Study contacts
- Principal investigator: Hamed M Wally Allah — Al-Azhar University
- Study coordinator: Hamed M Wally Allah, MSc
- Email: Hamed.mohamed@azhar.edu.eg
- Phone: 01067363929
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.