Transcutaneous Nerve Stimulation to Help Breathing After Bariatric Surgery
Official title: Effect of Transcutaneous Electrical Nerve Stimulation on Postoperative Diaphragmatic Dysfunction in Morbidly Obese Patients Undergoing Bariatric Surgery: A Randomized Controlled Trial
Run by Cairo University · NCT07569705 · Data updated 2026-11-12
A randomized trial tests whether a skin-placed nerve stimulator can reduce diaphragmatic dysfunction after bariatric surgery in people with obesity.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 20 Years to 60 Years |
| Sex | All |
| Enrollment | 70 (estimated) |
| Sponsor | Cairo University Academic / other |
| Locations | 2 sites (Cairo and 1 other locations) |
| Status | Recruiting |
| Started | May 17, 2026 |
| Main results expected | August 15, 2026 |
| Study ends | August 30, 2026 |
| Registry record updated | May 20, 2026 |
| Trial ID | NCT07569705 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults with BMI > 40 kg/m2 undergoing bariatric surgery and ASA II, with adequate ultrasound imaging.
✕Probably not a fit
Patients with preexisting pulmonary diseases or poor ultrasound windows may not benefit or may be excluded.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This randomized trial compares a transcutaneous electrical nerve stimulation (TENS) device to a sham device in morbidly obese patients undergoing bariatric surgery. Diaphragmatic function is measured by ultrasound, with dysfunction defined as diaphragmatic excursion under 10 mm. The study aims to see if TENS can improve postoperative diaphragmatic movement and potentially reduce respiratory complications. Eligible participants have BMI greater than 40 kg/m2 and ASA II; those with certain lung diseases or limited ultrasound views are excluded. The trial is led by Cairo University and conducted at Cairo University Hospitals.
Why it matters
Potential benefit: If successful, patients may experience better diaphragmatic function after surgery, which could improve breathing and recovery.
How similar studies have gone: Prior evidence supports diaphragmatic ultrasound as a reliable function measure in perioperative settings; the specific TENS approach for this indication is promising but requires confirmation.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Body mass index \> 40 kg/m2 * ASA II Exclusion Criteria: * Limited diaphragmatic ultrasound views * Patient with pulmonary diseases (COPD, bronchial asthma, and interstitial fibrosis) * Patient refusal
Where it's running
-
Cairo University Hospitals
Cairo, Egypt Recruiting -
Cairo University Hospitals
Cairo, Egypt Not yet recruiting
Study contacts
- Study coordinator: Mina Adolf Helmy, MD
- Email: minaadolf1988@cu.edu.eg
- Phone: 01275716942
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.