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NCT06294743

Posterior Tibia Nerve Neuroprolotherapy for Dysmenorrhea

Status unknown EARLY_PHASE1 Last updated 6 March 2024
What this trial tests

EARLY_PHASE1 trial testing Posterior tibial nerve neuroprolotherapy in Dysmenorrhea in 60 participants. Status unknown.

Timeline
23 November 2023
Primary endpoint
31 December 2025
31 December 2025

Quick facts

Lead sponsorTaichung Armed Forces General Hospital
PhaseEARLY_PHASE1
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingnone
Primary purposetreatment
Enrollment60
Start date23 November 2023
Primary completion31 December 2025
Estimated completion31 December 2025
Sites1 location across Taiwan

Drugs / interventions tested

Conditions studied

Sponsor

Taichung Armed Forces General Hospital

Who can join

Adults 18 to 50, female only, with Dysmenorrhea or Prolotherapy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this crossover study is to assessed the treatment efficacy of posterior tibia nerve neuroprolotherapy on dysmenorrhea. The primary outcome is the improvement of Visual Analogue Scale. The main question it aims to answer is: •Could the posterior tibial nerve neuroprolotherapy alleviate the pain of dysmenorrhea. Participants will be randomly allocated into two groups, Group-1 will receive neuroprolotherapy in the first 2 menstrual cycles followed by oral acetaminophen(500mg) for the subsequent 2 menstrual cycles. Group02 will received oral acetaminophen(500mg) in initial 2 menstrual cycles, followed by receiving neuroprolotherapy for the subsequent 2 menstrual cycles.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Dysmenorrhea

Currently open trials in the same condition.

Other Taichung Armed Forces General Hospital trials

Trials by the same sponsor.

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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/NCT06294743.

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