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A Visual Analogue Scale (VAS) Method for the Evaluation of Endometriosis related Pai

Not Applicable
Completed
Conditions
Endometriosis related Pain
Registration Number
JPRN-jRCTs031210592
Lead Sponsor
agashima Hirotaka
Brief Summary

The p-VAS and e-VAS were compared and examined as methods of assessing pain associated with endometriosis. The Brandt-Altman plot analysis showed that the p-VAS and e-VAS are highly consistent as methods for evaluating pain associated with endometriosis. The validity of the e-VAS as an alternative method to the p-VAS, which is based on the principle of 100 mm actual size, was confirmed in the evaluation of pain associated with endometriosis.

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
38
Inclusion Criteria

1.Japanese patients diagnosed with Endometriosis
2. Patients aged more than 20 years at the time of obtaining informed consent
3.To obtain a written informed consent from the patient for participation in the clinical trial

Exclusion Criteria

1.Patients who underwent any of the following procedures 2 months before the end of the last two menstruation cycles prior to obtaining written informed consent: cyst puncture (transvaginal alcohol fixation); laparotomy; or laparoscopic examination for endometriosis, adenomyosis, or uterine fibroids.
2.Patients with complications (excluding endometriosis) having an impact on pelvic pain assessment after the end of the last two menstruation cycles before obtaining written informed consent

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Values of p-VAS and e-VAS in pelvic pain (lower abdominal pain and low back pain)
Secondary Outcome Measures
NameTimeMethod
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