- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06102733
Chronic Pelvic Pain in Females and Males
Chronic Pelvic Pain Management in Female and Male Adult Patients
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.
Study Overview
Status
Conditions
Intervention / Treatment
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.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Olu Bamgbade, MD,FRCPC
- Phone Number: 17786286600
- Email: salem.painclinic@gmail.com
Study Contact Backup
- Name: Olumuyiwa Bamgbade, MD,FRCPC
- Phone Number: 17786286600
- Email: salem.painclinic@gmail.com
Study Locations
-
-
British Columbia
-
Surrey, British Columbia, Canada, V3S 7J1
- Recruiting
- Salem Anaesthesia Pain Clinic
-
Contact:
- Olu Bamgbade, MD,FRCPC
- Phone Number: 17786286600
- Email: salem.painclinic@gmail.com
-
Contact:
- Olumuyiwa Bamgbade, MD, FRCPC
- Phone Number: +17786286600
- Email: salem.painclinic@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
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
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Adult chronic pain patients
Adult chronic pain patients with pelvic, inguinal or sacroiliac pain
|
Chronic pain rehabilitation therapy
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Pain score, objective measurement using the validated Numeric Pain Rating scale
Time Frame: 12 months
|
Pain score, using the Numeric Pain Rating scale of 0 to 10, low scores indicate less pain, high scores indicate worse pain
|
12 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Olumuyiwa Bamgbade, MD,FRCPC, Salem Anaesthesia Pain Clinic
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Pathologic Processes
- Nervous System Diseases
- Pain
- Neurologic Manifestations
- Disease
- Neuromuscular Diseases
- Sciatic Neuropathy
- Mononeuropathies
- Peripheral Nervous System Diseases
- Neuralgia
- Nerve Compression Syndromes
- Pathological Conditions, Anatomical
- Hernia, Abdominal
- Hernia
- Syndrome
- Hernia, Inguinal
- Piriformis Muscle Syndrome
- Pelvic Pain
Other Study ID Numbers
- SalemAne2018 Pelvic Pain WoMen
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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