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Cyclic administration of Dienogest for dysmenorrhea in adenomyosis

Efficacy of a cyclic regimen of Dienogest for treatment of adenomyosis - NIL

Status
Unknown
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/02/062618
Enrollment
23
Registered
2024-02-14
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

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

Conditions

Health Condition 1: N800- Endometriosis of uterus

Interventions

Intervention1: Dienogest: 12-week course of cyclic regimen of Dienogest is given to all participant (21 days with 2 mg of dienogest starting on the first day of menstrual cycle followed by 7 drug free

Sponsors

Songklanagarind hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Adenomyosis is diagnosed by ultrasound 2.Dysmenorrhea with visual analog scale more than 3 3.Woman with regular frequency of menstruation 24-38 days for 3 cycles 4.No pregnancy desire during the treatment and trial period 5.No co-existing endometrioma or myoma or current PID by pelvic examination and ultrasonography

Exclusion criteria

Exclusion criteria: 1.Contraindication of dienogest 2.Previous hormonal treatment within 3 months or current use 3.History or suspicious of gynecologic malignancy or hormonal responsive tumor 4.Currently breastfeeding 5.Current use of drugs with interaction to cytochrome P450

Design outcomes

Primary

MeasureTime frame
To evaluate the change in visual analog scale (VAS) of dysmenorrhea during treatment women diagnosed with adenomyosis by cyclic regimen of dienogestTimepoint: 3 months

Secondary

MeasureTime frame
To evaluate adverse effect of cyclic regimen of dienogest.Timepoint: 3 months;To evaluate patterns and amount of uterine bleeding during treatment with cyclic regimen of dienogest.Timepoint: 3 months

Countries

Thailand

Contacts

Public ContactPakhanan Dankamak

Prince of Songklha University

Saranya.w@psu.ac.th66858842988

Outcome results

None listed

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