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Prediction of Response to IUCD Associated Menorrhagia Using Doppler

Assessment of Efficacy of Uterine Artery Doppler in Predicting the Response to Mefenamic Acid During Treatment of Women With IUCD Associated Menorrhagia

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03794895
Enrollment
156
Registered
2019-01-07
Start date
2017-05-01
Completion date
2018-05-01
Last updated
2019-01-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Women's Health: Amenorrhea/Dysmenorrhea

Brief summary

Studying the efficacy of uterine artery doppler in predicting response to mefenamic acid in women having IUCD associated menorrhagia

Interventions

DEVICEDoppler

Doing doppler for women having IUCD associated menorrhagia

Sponsors

Ain Shams University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SCREENING
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

* women in chile bearing period (age 20-35 yrs ) with history of regular menstrual cycle presenting with recent onset of more then three months menorrhagia after IUCD copper T 380 A insertion

Exclusion criteria

* history of bleeding tendency * history of abnormal uterine bleeding due to other causes * history of active liver disease * history of antiplatelet or anticoagulant intake in the last month * history of thyroid disease * history of endometritis * history of allergy to NSAIDs * Adenomyosis * women having contraindications to use NSAIDs e.g. peptic ulcer * Insulin dependant diabetes mellitus

Design outcomes

Primary

MeasureTime frameDescription
Resistance index and Pulsitality index (Predicting the response to IUCD associated menorrhagia)1 yearBase line uterine artery doppler is done to the patient complaining of IUCD related menorrhagia prior to treatment , parameters of doppler are: resistance index and pulsitality index, then the patient takes mefenamic acid tablets 500 mg three times daily for five days, assessment of response whether the patient is responder or not is done using pictorial blood loss assessment chart then base line doppler parameters in responders and non responders are compared to correlate the response to base line doppler parameters

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026