MedPath

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
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
ot 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
NameTimeMethod
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
NameTimeMethod
1.To correlate type of feature, number of features, site and extent of adenomyosis with quality of lifeTimepoint: zero weeks
© Copyright 2025. All Rights Reserved by MedPath