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Active rTMS to the DLPFC for patients undergoing major abdominal surgeryTrial plans to use magnetic pulses for abdominal surgery recovery

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Key Takeaway
Note that this is a study protocol for a planned trial; no clinical results are currently available.

This study protocol outlines a planned randomized controlled trial involving 208 participants undergoing major abdominal surgery. The study aims to evaluate the impact of noninvasive interventions on perioperative recovery and patient experience.

Participants will be randomized to receive either active repetitive transcranial magnetic stimulation (rTMS) to the dorsolateral prefrontal cortex (DLPFC) at 120% of the resting motor threshold (RMT) and 10 Hz, or a sham rTMS procedure. The primary outcome is the Quality of Recovery-15 (QoR-15) score at 24 hours postoperatively.

Secondary outcomes include QoR-15 scores at additional time points, pain intensity, delirium incidence, opioid consumption, postoperative nausea and vomiting (PONV), anxiety, patient satisfaction, and gastrointestinal recovery. Safety and tolerability data are not yet available.

As this is a protocol for a prospective trial, no results are reported. The study is designed to evaluate rTMS as a noninvasive adjunct in perioperative care. Clinical application cannot be determined until the trial is completed and data are analyzed.

Recovering from major abdominal surgery is often a long and difficult road. Patients frequently deal with intense pain, anxiety, and the physical stress of the procedure. Researchers are looking for ways to make this period easier and more comfortable for those undergoing these intense operations.

To do this, a new study plans to test a noninvasive treatment called repetitive transcranial magnetic stimulation (rTMS). This method uses magnetic pulses delivered to a specific part of the brain. The goal is to see if these pulses can improve a patient's quality of recovery and help manage symptoms like pain and nausea after surgery.

Because this is a study protocol, the trial has not been conducted yet. No results are available at this time. The study will involve 208 participants to see if this magnetic treatment can be a helpful addition to standard care for patients recovering from abdominal surgery.

What this means for you:
A new trial will test if magnetic brain stimulation helps patients recover from major abdominal surgery.

Common questions

What is the treatment being tested?

The trial plans to use repetitive transcranial magnetic stimulation (rTMS). This is a noninvasive method that uses magnetic pulses delivered to a specific part of the brain called the dorsolateral prefrontal cortex. The goal is to see if it helps patients during their recovery from abdominal surgery.

Are there any results from this study yet?

No results are available yet. This document is a study protocol, which means it is a plan for a future trial. The study has not been conducted yet, so no data on pain, anxiety, or recovery times are currently known.

Who will participate in this study?

The study plans to involve 208 participants. These will be individuals who are undergoing major abdominal surgery. The goal is to see if the magnetic treatment can be a helpful addition to their standard care.

Study Details

Study typeRct
EvidenceLevel 2
PublishedOct 2026
View Original Abstract ↓
Major abdominal surgery is a primary therapeutic strategy for various abdominal diseases, but it is often related to severe postoperative pain, complications, and delayed recovery. Repetitive transcranial magnetic stimulation (rTMS), a noninvasive neuromodulatory technique, may influence pain processing, emotional regulation, and other neural functions relevant to postoperative recovery. However, its role in improving quality of postoperative recovery remains insufficiently investigated, particularly with respect to patient-reported recovery outcomes. This investigation is a single-center, prospective, randomized controlled study. A total of 208 participants undergoing major abdominal surgery will be classified into receiving either active or sham rTMS in a random manner. Active stimulation will be delivered to the dorsolateral prefrontal cortex (DLPFC) at 120% of the resting motor threshold (RMT) and 10 Hz. The primary outcome is the Quality of Recovery-15 (QoR-15) score at 24 h postoperatively. Exploratory secondary outcomes include QoR-15 scores at additional time points, pain intensity, delirium incidence, opioid consumption, postoperative nausea and vomiting (PONV), anxiety, patient satisfaction, and gastrointestinal recovery. Safety outcomes include adverse events (AEs). We will conduct the primary analysis according to the intention-to-treat (ITT) principle, comprising all randomized participants. This investigation is designed to estimate whether rTMS can enhance quality of postoperative recovery in participants experiencing a major abdominal operation. The outcomes will provide evidence about the potential role of rTMS as a noninvasive adjunct in perioperative care and inform future multicenter trials. Clinical Trial registration:https://www.chictr.org.cn/index.html, identifier ChiCTR2600119250.
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