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Erector Spinae Plane Block and Its Impact on Postoperative Diaphragmatic Dysfunction in Morbidly Obese Patients Undergoing Laparoscopic Sleeve Gastrectomy

Erector Spinae Plane Block and Its Impact on Postoperative Diaphragmatic Dysfunction in Morbidly Obese Patients Undergoing Laparoscopic Sleeve Gastrectomy, A Double-blind Randomized Control Trial.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07022600
Enrollment
80
Registered
2025-06-15
Start date
2025-05-27
Completion date
2025-07-31
Last updated
2025-09-18

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

Conditions

Diaphragmatic Dysfunction

Keywords

erector spinae block, diaphragmatic dysfunction, morbidly obese

Brief summary

postoperative diaphragmatic dysfunction is critical especially in morbidly obese patients

Detailed description

Investigators aimed to evaluate the impact of erector spinae plane block on the incidence of postoperative diaphragmatic dysfunction in morbidly obese patients (Body mass index more than or equal 40)

Interventions

diaphragmatic excursion will be conducted at baseline and at 2 and 24 hours postoperatively

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* morbidly obese (body mass index\> 40) * undergoing sleeve gastrectomy

Exclusion criteria

* allergy to bupivacaine * respiratory comorbidities * preoperative diaphragmatic dysfunction * Patient refusal * inability to adequately visualize diaphragm

Design outcomes

Primary

MeasureTime frameDescription
Incidence of diaphragmatic dysfunction in both groupsbaseline and 2 hours after surgerypostoperative diaphragmatic excursion 10 mm at 2 hours after surgery

Secondary

MeasureTime frameDescription
Forced expiratory volume at one secondat baseline, 2 and 24 hours postoperativelyFEV1 (in liter)
numeric rating scaleat 24 hours after surgeryscore from zero to 10
Forced vital capacity (in Liter)at baseline, 2 hours, and 24 hours after surgeryFVC (in liter)
Peak expiratory flow rate (Liter/sec)baseline, 2 hours, and 24 hoursPEFR (Liter/sec)

Countries

Egypt

Outcome results

None listed

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