relation of clinical symptoms of pain and heavy menstrual bleeding in adenomyosis with ultrasound features as mentioned in revised Morphological Ultrasonographic Assessment (MUSA) features
Not Applicable
Not yet recruiting
- Conditions
- Health Condition 1: N858- Other specified noninflammatory disorders of uterus
- Registration Number
- CTRI/2023/12/060484
- Lead Sponsor
- AIIMS New Delhi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients presenting with symptoms of dysmenorrhea/HMB/ and
Diagnosed to have adenomyosis based on ? 1 ultrasound features of adenomyosis as per revised MUSA criteria
Willing to give informed written consent
Exclusion Criteria
Coexisting fibroid (Fibroid >5 cm or FIGO type 0,1,2)
Coexisting endometriosis
Women using contraceptives or taking hormonal medications within 3 months of recruitment
Not willing to give consent for the study
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1.Correlation of pain score (NRS4) with direct/indirect features, number of features, site and extent of adenomyosis <br/ ><br>2.Correlation of total menstrual loss by PBAC(PBAC100) with direct/indirect features, number of features, site and extent of adenomyosis <br/ ><br>Timepoint: patient assessment at a given point only, no follow up required <br/ ><br>
- Secondary Outcome Measures
Name Time Method 1.To correlate type of feature, number of features, site and extent of adenomyosis with quality of lifeTimepoint: zero weeks