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Recruiting NCT07104825

NCT07104825 Autonomic Neural Blockade in Bariatric Surgery

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Clinical Trial Summary
NCT ID NCT07104825
Status Recruiting
Phase —
Sponsor Endeavor Health
Condition Bariatric Surgery Candidate
Study Type INTERVENTIONAL
Enrollment 200 participants
Start Date 2026-02-05
Primary Completion 2027-12

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 90 Years
Study Type INTERVENTIONAL
Interventions
Intraoperative autonomic neural blockade (ANB)Laparoscopic Standard of Care Abdominal Wall Block

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

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 200 participants in total. It began in 2026-02-05 with a primary completion date of 2027-12.

⚠ 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

The purpose of this research is to evaluate if autonomic nerve block (ANB- blocking pain and nausea signals) decreases pain and anti-nausea medication requirements as well as the experience of pain/nausea during the first 72 hours after sleeve gastrectomy or gastric bypass surgery. Participants will be randomly assigned either to the standard of care or the ANB group before surgery. As part of standard of care, in both groups, laparoscopic bariatric surgery will be initiated with local anesthetic injected into the abdominal wall. In the ANB group, participants will be given an additional injection of local anesthetic medication to block nerves on and around the stomach.

Eligibility Criteria

Inclusion Criteria: * Individuals able and willing to consent and participate in all study activities * Adults, ages 18-90 * All patients with severe obesity undergoing laparoscopic/robotic gastric bypass or sleeve gastrectomy Exclusion Criteria: * Patients taking opiates chronically * Patients allergic to study medications * Patients with any prior adverse reaction to ingredients included in the block * Adults unable to consent * Pregnant women * Prisoners

Contact & Investigator

Central Contact

Herbert Hedberg, MD

✉ herbert.hedberg@endeavorhealth.org

📞 508-728-2106

Principal Investigator

Herbert Hedberg, MD

PRINCIPAL INVESTIGATOR

Endeavor Health

Frequently Asked Questions

Who can join the NCT07104825 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 90 Years, studying Bariatric Surgery Candidate. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07104825 currently recruiting?

Yes, NCT07104825 is actively recruiting participants. Contact the research team at herbert.hedberg@endeavorhealth.org for enrollment information.

Where is the NCT07104825 trial being conducted?

This trial is being conducted at Evanston, United States.

Who is sponsoring the NCT07104825 clinical trial?

NCT07104825 is sponsored by Endeavor Health. The principal investigator is Herbert Hedberg, MD at Endeavor Health. The trial plans to enroll 200 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology