NCT07569705 Effect of Transcutaneous Electrical Nerve Stimulation on PODD in Bariatric Surgery Patients
| NCT ID | NCT07569705 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Cairo University |
| Condition | Bariatric Surgery |
| Study Type | INTERVENTIONAL |
| Enrollment | 70 participants |
| Start Date | 2026-05-17 |
| Primary Completion | 2026-08-15 |
Eligibility & Interventions
Eligibility Fast-Check
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What to Expect as a Participant
You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.
This trial targets 70 participants in total. It began in 2026-05-17 with a primary completion date of 2026-08-15.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
Researchers aim to evaluate impact of transcutaneous electric nerve stimulator on the incidence of postoperative diaphragmatic dysfunction in patients living with obesity undergoing bariatric surgery
Eligibility 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
Contact & Investigator
Frequently Asked Questions
Who can join the NCT07569705 clinical trial?
This trial is open to participants of all sexes, aged 20 Years or older, up to 60 Years, studying Bariatric Surgery. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07569705 currently recruiting?
Yes, NCT07569705 is actively recruiting participants. Contact the research team at minaadolf1988@cu.edu.eg for enrollment information.
Where is the NCT07569705 trial being conducted?
This trial is being conducted at Cairo, Egypt, Cairo, Egypt.
Who is sponsoring the NCT07569705 clinical trial?
NCT07569705 is sponsored by Cairo University. The trial plans to enroll 70 participants.