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NCT05851742

Effects of Myofascial Release and Electrical Stimulation in Chronic Pelvic Pain

Status unknown NA Last updated 10 May 2023
What this trial tests

NA trial testing TENS in Chronic Pelvic Pain in 24 participants. Status unknown.

Timeline
1 January 2023
Primary endpoint
1 July 2023
1 August 2023

Quick facts

Lead sponsorRiphah International University
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment24
Start date1 January 2023
Primary completion1 July 2023
Estimated completion1 August 2023
Sites1 location across Pakistan

Drugs / interventions tested

Conditions studied

Sponsor

Riphah International University

Who can join

Adults 25 to 45, female only, with Chronic Pelvic Pain or Myofascial Trigger Point Pain. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Myofascial pelvic pain (MFPP) caused by myofascial trigger points (MTrPs) is a major contributor to chronic pelvic pain in women.In females,pelvic pain is the single most common indication for referral to women's health services.Pelvic floor physical therapy with myofascial release improve mobility and reduce pain by releasing the painful trigger points.Tools that will be used,for pain numerical pain scale (NPS),functional pelvic pain scale(FPPS) and pelvic floor impact questionnaire-7 will be used to asses pain and functionality.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of TENS

Trials testing the same drug.

Other recruiting trials for Chronic Pelvic Pain

Currently open trials in the same condition.

Other Riphah International University 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/NCT05851742.

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