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NCT06795594

Effectiveness of Cheek Acupuncture Therapy for Pain Control After Cesarean Delivery

Completed NA Last updated 25 March 2025
What this trial tests

NA trial testing cheek acupuncture in Acupuncture Analgesia in 80 participants. Completed in 10 March 2025.

Timeline
5 January 2025
Primary endpoint
10 March 2025
10 March 2025

Quick facts

Lead sponsorBeijing Tongren Hospital
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Enrollment80
Start date5 January 2025
Primary completion10 March 2025
Estimated completion10 March 2025
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Beijing Tongren Hospital

Who can join

Adults 18 to 45, female only, with Acupuncture Analgesia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study investigates whether cheek acupuncture therapy can alleviate postoperative pain in cesarean section patients and explores its mechanisms of action through a prospective randomized controlled clinical trial.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of cheek acupuncture

Trials testing the same drug.

Other recruiting trials for Acupuncture Analgesia

Currently open trials in the same condition.

Other Beijing Tongren Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06795594.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing