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Clinical Trial

tDCS for Reducing the Incidence of OEI After Cesarean Section

NCT: NCT07569783 · NOT_YET_RECRUITING

NCT IDNCT07569783
StatusNOT_YET_RECRUITING
Start Date2026-05-01
Completion2027-02-20

Brief Summary

Cesarean section is the most common obstetric surgery worldwide. Epidural anesthesia has become the preferred anesthesia method for cesarean sections due to its definite analgesic effect and minimal impact on mother and baby. To ensure postoperative analgesia, intrathecal administration of morphine (the preferred opioid for obstetric intrathecal analgesia) is a routine clinical protocol, but morphine-induced postoperative pruritus is a common adverse reaction. A study targeting the cesarean section population confirmed that the incidence of pruritus after epidural morphine administration is as high as 40%-75%.Transcranial direct current stimulation (tDCS) can enhance the activity of GABAergic inhibitory interneurons in the spinal dorsal horn through the cortical-spinal descending pathway, reverse the inhibitory effect of morphine on them, and restore negative feedback regulation of itch-specific GRPR⁺ neurons; at the same time, it downregulates the phosphorylation level and membrane expression of μ-opioid receptors in the spinal dorsal horn, weakening the receptor activation efficiency of morphine. On the other hand, tDCS can reduce peripheral nerve excitability, decrease mast cell degranulation in the skin, and reduce the release of histamine and tryptase; simultaneously, it inhibits the activation of glial cells in the spinal cord/cortex, decreases the secretion of pro-inflammatory factors such as TNF-α and IL-6, and blocks the vicious cycle of 'inflammation-receptor upregulation-itch exacerbation,' thereby reducing the occurrence of itch.This study aims to explore the effect of transcranial direct current stimulation (tDCS) on the incidence of morphine-induced itching after cesarean section by inhibiting the central itch perception circuits in cesarean section patients and antagonizing the disinhibitory effects mediated by μ-opioid receptors in the spinal dorsal horn.

Frequently Asked Questions

What is tDCS for Reducing the Incidence of OEI After Cesarean Section?

tDCS for Reducing the Incidence of OEI After Cesarean Section is a clinical trial registered under NCT07569783. Current status: NOT_YET_RECRUITING.

What is the status of NCT07569783?

The current status of NCT07569783 (tDCS for Reducing the Incidence of OEI After Cesarean Section) is: NOT_YET_RECRUITING.

When did tDCS for Reducing the Incidence of OEI After Cesarean Section start?

tDCS for Reducing the Incidence of OEI After Cesarean Section started on 2026-05-01.

Official Source

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Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.