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NCT06730776

Effect of Transcutaneous Electrical Acupoint Stimulation on Dyspareunia

Not yet recruiting NA Last updated 12 December 2024
What this trial tests

NA trial testing Topical medication in Dyspareunia (Female) in 38 participants. Not yet recruiting.

Timeline
15 December 2024
Primary endpoint
15 May 2025
30 May 2025

Quick facts

Lead sponsorCairo University
PhaseNA
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment38
Start date15 December 2024
Primary completion15 May 2025
Estimated completion30 May 2025
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Cairo University

Who can join

Adults 25 to 35, female only, with Dyspareunia (Female). Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Transcutaneous electrical acupoint stimulation (TEAS)was proven to stimulate the secretion of endogenous opioid peptides which are partial substitutes for the exogenous opioids stimulated by drugs in the central nervous system and can thus relieve pain. Till now there is no previous study that investigates the effect of TEAS on dyspareunia. This study will determine the effect of transcutaneous acupoint stimulation on dyspareunia. Patients will be divided randomly into two groups equal in number: The control group will receive only topical medication. The study group will receive Acu-TENS and topical medication.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Cairo University 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/NCT06730776.

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