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Recruiting NCT06102733

Chronic Pelvic Pain in Females and Males

— Observational Pelvic Pain Syndrome Sacroiliac Disorder Piriformis Syndrome Sacrococcygeal Disorder

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Rehabilitation therapy.
Who it may be relevant to
Registry conditions: Pelvic Pain Syndrome, Sacroiliac Disorder, Piriformis Syndrome, Sacrococcygeal Disorder. Basic parameters: 20 years — 99 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Canada
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Chronic Pelvic Pain Management in Female and Male Adult Patients

Overview

Pelvic pain is under-reported in healthy adults. Many patients with pelvic pain under-estimate the problem. Chronic pelvic pain can be managed properly, if diagnosed promptly. This is a quantitative analysis of prospective clinical data. It evaluates the management of pelvic pain in a cohort population, and analyzes the treatment outcome.

Detailed description

Pelvic pain is common, but under-reported in healthy adults. Pelvic pain is reported more commonly in women than in men. Many patients with pelvic pain under-estimate the severity of the problem. Chronic pelvic pain can be managed successfully, if diagnosed properly. Many combinations of multimodal analgesia and rehabilitation therapy may be safe and effective for pelvic pain.

This study is a quantitative analysis of prospective clinical data. It is an evaluation of the prevalence and management of pelvic pain in a cohort population of chronic pain patients. This is an analysis of multimodal analgesia types, rehabilitation therapy types, treatment outcome, and complications.

Interventions

  • Behavioral Rehabilitation therapy
    Chronic pain rehabilitation therapy

Primary outcome measures

  • Pain score, objective measurement using the validated Numeric Pain Rating scale [Time frame: 12 months]

Eligibility criteria

Inclusion criteria

  • Patients with chronic pelvic pain
  • Patients with sacroiliac pain
  • Patients with inguinal pain
  • Patients with coccygeal pain
  • Patients with piriformis pain

Exclusion criteria

  • Patients with spinal pain
  • Patients who had spine surgery

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

Canada · 1 center
  • Salem Anaesthesia Pain Clinic — Surrey

Identifiers

NCT: NCT06102733 · SalemAne2018 Pelvic Pain WoMen

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗