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NCT01802528 Clinical Trial

Clinical Effectiveness of Obturator Externus Muscle Injection in Chronic Pelvic Pain Patients

Chronic Pelvic Pain Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01802528
Other study ID # 4-2012-0924
Secondary ID
Status Completed
Phase N/A
First received February 27, 2013
Last updated February 27, 2013
Start date March 2012
Est. completion date December 2012

Study information
Verified date February 2013
Source Yonsei University
Contact n/a
Is FDA regulated No
Health authority Korea: Institutional Review Board
Study type Observational

Clinical Trial Summary

Obturator externus (OE) muscle has the possibility as a pain generator, considering its anatomical and functional aspects, but this muscle as a possible target for therapeutic intervention is currently understudied in pain practice.

Recruitment information / eligibility
Status Completed
Enrollment 23
Est. completion date December 2012
Est. primary completion date December 2012
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 75 Years
Eligibility Inclusion Criteria:

- 1. 20-75 adults/ 2. Chronic pelvic pain patients who required the interventional procedures/ 3. patients with a localized tenderness on inferolateral side of the pubic tubercle

Exclusion Criteria:

- 1. Severe cardiovascular disease /2. Coagulation abnormality /3. Patient denial

Study Design

Observational Model: Cohort, Time Perspective: Retrospective

Related Conditions & MeSH terms

Locations
Country Name City State
Korea, Republic of Department of Anesthesiology and Pain Medicine, Anesthesia and Pain Research Institute, Seoul

Sponsors (1)
Lead Sponsor Collaborator
Yonsei University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary Post-injection pain score Before and after the OE muscle injection, patients were asked to rate their pain score using a 10-point numeric rating scale (NRS; 0=no pain, 10=worst possible pain). We also assessed the degree of patient satisfaction as excellent, good, fair, and bad during 2 weeks after injection. In this period, any analgesic medications did not change in all patients. Complications associated with OE muscle injection were investigated. at 2 weeks after injection No
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