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Neurophysiological Validation of the Clinical Criteria of Sensitization in Chronic Pelvic and Perineal Pain Population

NCT03541954 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2022-04-05

No results posted yet for this study

Summary

The purpose of this study is to assess and validate the clinical criteria of sensitization ("Convergences PP criteria") selected by the expert consensus with neurophysiological sensory testing.

Conditions

  • Chronic Pelvic Pain
  • Chronic Perineal Pain

Interventions

OTHER

Sensory testing of lower urinary tract.

Non invasive lower urinary tract sensitivity testing: provoked diuresis with sonographic estimates of sensory thresholds.

OTHER

Sensory testing of lower rectal tract

Lower digestive tract sensitivity testing: rectal electronic barostat with ascending pressure (phasic distension).

OTHER

Sensory testing of vulva muscles

Vulvar sensitivity testing: pressure pain threshold evaluated using vulvagesiometer.

OTHER

Sensory testing of pelvic muscles

Myofascial sensitivity testing: piriformis, levator ani and obturator internus muscles pressure pain threshold evaluated using intra-vaginal algometer.

Sponsors & Collaborators

  • Nantes University Hospital

    lead OTHER

Study Design

Allocation
NON_RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
25 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-07-17
Primary Completion
2022-02-14
Completion
2022-02-14

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03541954 on ClinicalTrials.gov