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Comparison effect ofmefenamic acid and tranexamic acid in the treatment of bleeding secondary to the use of IUD

Comparison effect ofmefenamic acid and tranexamic acid ontreatmentofmenorrhagiasecondrydueIUD(TCU380)user referring to health clinic in Bandarabbass1390

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT201205092515N8
Enrollment
84
Registered
2012-07-05
Start date
2011-09-30
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

menorrhagia.

Interventions

Tranksymyk acid 250 mg capsule three times a day (every 8 hours) Mefenamic acid 250 mg capsule three times a day (every 8 hours).
Treatment - Drugs
Tranksymyk acid 250 mg capsule three times a day (every 8 hours) Mefenamic acid 250 mg capsule three times a day (every 8 hours)

Sponsors

Vice chancellor for research, Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Inclusion criteria: willingness to cooperate in women using TCU380 (IUD); no experiment coagulation disorders and systemic disorders; none ultrasound malignancies; counting padding to verify menorrhagia; none use of other methods of contraception; no disease of the digestive and liver, brain and kidney; no trombosis; no history of allergy to mefenamic acid and hemoglobin; no history thrombosis and clotting disorders; no history of irregular uterine bleeding; uterine size between 9-6 cm; hemoglobin above 10; having 1 to 5 parity and no unwanted pregnancy. Exclusion criteria: sensitivity to the drug use the drug note continued; dissatisfaction with the plan; unwanted pregnancy with IUD and IUD removal.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Menorrhagia. Timepoint: before intervention and first and second months after intervention. Method of measurement: PBAC Table.

Secondary

MeasureTime frame
Side effects. Timepoint: One month and two months after intervention. Method of measurement: Standard questionnaire.

Countries

Iran (Islamic Republic of)

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026