Clinical Trials Directory

Trials / Completed

CompletedNCT07277478

Effects of Auricular Acupressure on Relieving Pain in Postpartum Women With Episiotomy

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
90 (actual)
Sponsor
HSIAO AI WEN · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Accepted

Summary

This randomized, single-blind controlled trial examined the effects of auricular acupressure on postpartum women who underwent episiotomy. A total of 86 participants were allocated to either an intervention group, which received routine care plus transparent auricular patches containing magnetic beads applied to selected acupoints, or a control group, which received identical patches without magnetic beads. The patches were applied for 48 hours after delivery. Perineal pain and its impact on daily activities were assessed at 2, 12, 24, and 48 hours postpartum, while satisfaction with perineal pain care was measured at 48 hours. Using independent t-tests, chi-square tests, and generalized estimating equations, the study evaluated whether auricular acupressure reduced perineal wound pain, lessened pain-related interference with daily activities, and improved satisfaction with perineal pain management.

Conditions

Interventions

TypeNameDescription
DEVICEauricular patchAfter placental delivery, the intervention group received routine care plus a transparent patented auricular patch containing magnetic beads, while the control group received a transparent patented auricular patch without magnetic beads. The selected acupoints included internal genitalia (TF2), external genitalia (HX4), Shenmen (TF4), sympathetic (AH6a), and subcortex (AT4)

Timeline

Start date
2024-12-07
Primary completion
2025-04-10
Completion
2025-09-12
First posted
2025-12-11
Last updated
2025-12-11

Locations

1 site across 1 country: Taiwan

Source: ClinicalTrials.gov record NCT07277478. Inclusion in this directory is not an endorsement.