NCT07591558

Brief Summary

Atelectasis is considered a common complication in the perioperative period, especially following surgeries under general anesthesia. Postoperative atelectasis could occur anytime during the perioperative period from intraoperative period to 24 hours postoperative and contribute to a variety of other complications, including hypoxemia and pneumonia. In the literature, several methods were utilized to combat this phenomenon, therefore, we investigate the role of intraoperative salbutamol in reducing the incidence of atelectasis. It is well known that salbutamol could be an adjunctive bronchodilator medication used in the intraoperative anesthetic regimens.

Trial Health

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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
80

participants targeted

Target at P75+ for early_phase_1

Timeline
6mo left

Started Jun 2026

Shorter than P25 for early_phase_1

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 3, 2026

Completed
12 days until next milestone

First Posted

Study publicly available on registry

May 15, 2026

Completed
17 days until next milestone

Study Start

First participant enrolled

June 1, 2026

Expected
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 1, 2026

2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2026

Last Updated

May 15, 2026

Status Verified

May 1, 2026

Enrollment Period

4 months

First QC Date

May 3, 2026

Last Update Submit

May 11, 2026

Conditions

Keywords

atelectasissalbutamolpulmonarybronchodilator

Outcome Measures

Primary Outcomes (3)

  • Postoperative atelectasis (vital signs)

    All patients will undergo a thorough medical history, appropriate physical examination, and relevant investigations according to their clinical needs. Particular attention will be given to vital signs, especially pulse oximetry.

    5 months

  • Postoperative atelectasis (x-ray)

    All patients will undergo a chest X-ray to investigate for atelectasis.

    5 months

  • Postoperative atelectasis (blood gases)

    Postoperatively blood gases will be assessed to investigate for atelectasis. This will be done through arterial blood gases sample at 24 hours postoperative.

    5 months

Study Arms (4)

salbutamol group for diabetic patients

EXPERIMENTAL

for diabetic patients

Drug: Salbutamol (Ventolin®)

no intervention for diabetic

NO INTERVENTION

salbutamol group for non-diabetic patients

EXPERIMENTAL

for non-diabetic patients

Drug: Salbutamol (Ventolin®)

no intervention for non-diabetic patients

NO INTERVENTION

for non-diabetic patients

Interventions

-4 puffs of salbutamol (each puff = 100 µg, total dose 200-400 µg)

salbutamol group for diabetic patientssalbutamol group for non-diabetic patients

Eligibility Criteria

Age18 Years - 70 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • The study will include patients aged 18-70 years
  • American Society of Anesthesiologists (ASA) physical status of I or II
  • Will undergo thoracic, abdominal or spinal surgery

You may not qualify if:

  • cardiac conditions other than hypertension like arrhythmia
  • previous cardiac surgeries and valvular heart diseases

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

King Abdullah University Hospital

Irbid, Jordan

Location

MeSH Terms

Conditions

Pulmonary AtelectasisDiabetes Mellitus

Interventions

Albuterol

Condition Hierarchy (Ancestors)

Lung DiseasesRespiratory Tract DiseasesGlucose Metabolism DisordersMetabolic DiseasesNutritional and Metabolic DiseasesEndocrine System Diseases

Intervention Hierarchy (Ancestors)

EthanolaminesAmino AlcoholsAlcoholsOrganic ChemicalsAminesPhenethylaminesEthylamines

Central Study Contacts

Diab Bani Hani Bani Hani

CONTACT

Study Design

Study Type
interventional
Phase
early phase 1
Allocation
RANDOMIZED
Masking
QUADRUPLE
Who Masked
PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor of Anesthesia

Study Record Dates

First Submitted

May 3, 2026

First Posted

May 15, 2026

Study Start (Estimated)

June 1, 2026

Primary Completion (Estimated)

October 1, 2026

Study Completion (Estimated)

December 1, 2026

Last Updated

May 15, 2026

Record last verified: 2026-05

Data Sharing

IPD Sharing
Will not share

Locations